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Imaging axonal transport in the rat visual pathwayCarla J. Abbott, Tiffany E. Choe, Theresa A. Lusardi, Claude F. Burgoyne, Lin Wang, and Brad Fortune »View Author Affiliations
Carla J. Abbott,1
Tiffany E. Choe,1
Theresa A. Lusardi,2
Claude F. Burgoyne,1
Lin Wang,1
and Brad Fortune1,*
1Discoveries in Sight Research Laboratories, Devers Eye Institute, and Legacy Research Institute, Legacy Health, Portland, OR 97232, USA 2R.S. Dow Neurobiology Laboratories, Legacy Research Institute, Legacy Health, Portland, OR 97232, USA *Corresponding author: bfortune@deverseye.org |
Biomedical Optics Express, Vol. 4, Issue 2, pp. 364-386 (2013)
http://dx.doi.org/10.1364/BOE.4.000364
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Abstract
A technique was developed for assaying axonal transport in retinal ganglion cells using 2 µl injections of 1% cholera toxin b-subunit conjugated to AlexaFluor488 (CTB). In vivo retinal and post-mortem brain imaging by confocal scanning laser ophthalmoscopy and post-mortem microscopy were performed. The transport of CTB was sensitive to colchicine, which disrupts axonal microtubules. The bulk rates of transport were determined to be approximately 80–90 mm/day (anterograde) and 160 mm/day (retrograde). Results demonstrate that axonal transport of CTB can be monitored in vivo in the rodent anterior visual pathway, is dependent on intact microtubules, and occurs by active transport mechanisms.
© 2013 OSA
OCIS Codes
(170.3880) Medical optics and biotechnology : Medical and biological imaging
(170.2655) Medical optics and biotechnology : Functional monitoring and imaging
ToC Category:
Functional Imaging
History
Original Manuscript: November 19, 2012
Revised Manuscript: January 10, 2013
Manuscript Accepted: January 28, 2013
Published: January 30, 2013
Citation
Carla J. Abbott, Tiffany E. Choe, Theresa A. Lusardi, Claude F. Burgoyne, Lin Wang, and Brad Fortune, "Imaging axonal transport in the rat visual pathway," Biomed. Opt. Express 4, 364-386 (2013)
http://www.opticsinfobase.org/boe/abstract.cfm?URI=boe-4-2-364
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References
- A. Brown, “Axonal transport of membranous and nonmembranous cargoes: a unified perspective,” J. Cell Biol.160(6), 817–821 (2003). [CrossRef] [PubMed]
- R. D. Vale and R. A. Milligan, “The way things move: looking under the hood of molecular motor proteins,” Science288(5463), 88–95 (2000). [CrossRef] [PubMed]
- A. J. Reynolds, S. E. Bartlett, and I. A. Hendry, “Molecular mechanisms regulating the retrograde axonal transport of neurotrophins,” Brain Res. Brain Res. Rev.33(2-3), 169–178 (2000). [CrossRef] [PubMed]
- P. J. Hollenbeck and W. M. Saxton, “The axonal transport of mitochondria,” J. Cell Sci.118(23), 5411–5419 (2005). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- J. O. Johansson, “Retrograde axoplasmic transport in rat optic nerve in vivo. What causes blockage at increased intraocular pressure?” Exp. Eye Res.43(4), 653–660 (1986). [CrossRef] [PubMed]
- J. O. Johansson, “Inhibition and recovery of retrograde axoplasmic transport in rat optic nerve during and after elevated IOP in vivo,” Exp. Eye Res.46(2), 223–227 (1988). [CrossRef] [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- D. R. Anderson and A. Hendrickson, “Effect of intraocular pressure on rapid axoplasmic transport in monkey optic nerve,” Invest. Ophthalmol.13(10), 771–783 (1974). [PubMed]
- H. Quigley and D. R. Anderson, “The dynamics and location of axonal transport blockade by acute intraocular pressure elevation in primate optic nerve,” Invest. Ophthalmol.15(8), 606–616 (1976). [PubMed]
- H. A. Quigley, J. Guy, and D. R. Anderson, “Blockade of rapid axonal transport. Effect of intraocular pressure elevation in primate optic nerve,” Arch. Ophthalmol.97(3), 525–531 (1979). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Breakdown of the normal optic nerve head blood-brain barrier following acute elevation of intraocular pressure in experimental animals,” Invest. Ophthalmol. Vis. Sci.19(3), 244–255 (1980). [PubMed]
- H. A. Quigley and D. R. Anderson, “Distribution of axonal transport blockade by acute intraocular pressure elevation in the primate optic nerve head,” Invest. Ophthalmol. Vis. Sci.16(7), 640–644 (1977). [PubMed]
- R. L. Radius, E. L. Schwartz, and D. R. Anderson, “Failure of unilateral carotid artery ligation to affect pressure-induced interruption of rapid axonal transport in primate optic nerves,” Invest. Ophthalmol. Vis. Sci.19(2), 153–157 (1980). [PubMed]
- D. S. Minckler, A. H. Bunt, and G. W. Johanson, “Orthograde and retrograde axoplasmic transport during acute ocular hypertension in the monkey,” Invest. Ophthalmol. Vis. Sci.16(5), 426–441 (1977). [PubMed]
- D. S. Minckler, A. H. Bunt, and I. B. Klock, “Radioautographic and cytochemical ultrastructural studies of axoplasmic transport in the monkey optic nerve head,” Invest. Ophthalmol. Vis. Sci.17(1), 33–50 (1978). [PubMed]
- D. Gaasterland, T. Tanishima, and T. Kuwabara, “Axoplasmic flow during chronic experimental glaucoma. 1. Light and electron microscopic studies of the monkey optic nervehead during development of glaucomatous cupping,” Invest. Ophthalmol. Vis. Sci.17(9), 838–846 (1978). [PubMed]
- P. W. Lampert, M. H. Vogel, and L. E. Zimmerman, “Pathology of the optic nerve in experimental acute glaucoma. Electron microscopic studies,” Invest. Ophthalmol.7(2), 199–213 (1968). [PubMed]
- R. L. Radius and D. R. Anderson, “Reversibility of optic nerve damage in primate eyes subjected to intraocular pressure above systolic blood pressure,” Br. J. Ophthalmol.65(10), 661–672 (1981). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Rapid axonal transport in primate optic nerve. Distribution of pressure-induced interruption,” Arch. Ophthalmol.99(4), 650–654 (1981). [CrossRef] [PubMed]
- H. A. Quigley and E. M. Addicks, “Chronic experimental glaucoma in primates. II. Effect of extended intraocular pressure elevation on optic nerve head and axonal transport,” Invest. Ophthalmol. Vis. Sci.19(2), 137–152 (1980). [PubMed]
- L. Dandona, A. Hendrickson, and H. A. Quigley, “Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus,” Invest. Ophthalmol. Vis. Sci.32(5), 1593–1599 (1991). [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- X. C. Wan, J. Q. Trojanowski, and J. O. Gonatas, “Cholera toxin and wheat germ agglutinin conjugates as neuroanatomical probes: their uptake and clearance, transganglionic and retrograde transport and sensitivity,” Brain Res.243(2), 215–224 (1982). [CrossRef] [PubMed]
- J. Q. Trojanowski, J. O. Gonatas, and N. K. Gonatas, “Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP,” Brain Res.231(1), 33–50 (1982). [CrossRef] [PubMed]
- P. H. Luppi, P. Fort, and M. Jouvet, “Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons,” Brain Res.534(1-2), 209–224 (1990). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, and H. J. Karten, “The transport rate of cholera toxin B subunit in the retinofugal pathways of the chick,” Neuroscience92(2), 665–676 (1999). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- S. Reuss and K. Decker, “Anterograde tracing of retinohypothalamic afferents with Fluoro-Gold,” Brain Res.745(1-2), 197–204 (1997). [CrossRef] [PubMed]
- M. D. Fleming, R. M. Benca, and M. Behan, “Retinal projections to the subcortical visual system in congenic albino and pigmented rats,” Neuroscience143(3), 895–904 (2006). [CrossRef] [PubMed]
- N. Rivera and N. Lugo, “Four retinal ganglion cell types that project to the superior colliculus in the thirteen-lined ground squirrel (Spermophilus tridecemlineatus),” J. Comp. Neurol.396(1), 105–120 (1998). [CrossRef] [PubMed]
- M. E. Schwab and H. Thoenen, “Retrograde axonal and transsynaptic transport of macromolecules: physiological and pathophysiological importance,” Agents Actions7(3), 361–368 (1977). [CrossRef] [PubMed]
- J. D. Mikkelsen, “Visualization of efferent retinal projections by immunohistochemical identification of cholera toxin subunit B,” Brain Res. Bull.28(4), 619–623 (1992). [CrossRef] [PubMed]
- A. Angelucci, F. Clascá, and M. Sur, “Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains,” J. Neurosci. Methods65(1), 101–112 (1996). [CrossRef] [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
- M. Hirakawa, J. T. McCabe, and M. Kawata, “Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit,” Cell Tissue Res.267(3), 419–427 (1992). [CrossRef] [PubMed]
- S. Ochs, “Fast transport of materials in mammalian nerve fibers,” Science176(4032), 252–260 (1972). [CrossRef] [PubMed]
- S. Inoue, “The effect of colchicine on the microscopic and submicroscopic structure of the mitotic spindle,” Exp. Cell Res. Suppl.2, 305–318 (1952).
- O. J. Eigsti, “A cytological study of colchicine effects in the induction of polyploidy in plants,” Proc. Natl. Acad. Sci. U.S.A.24(2), 56–63 (1938). [CrossRef] [PubMed]
- O. J. Eigsti and P. D. Dustin, Jr., Colchicine— in Agriculture, Medicine, Biology and Chemistry (Iowa State College Press, Ames, IA, 1955)
- A. Dahlström, “Effect of colchicine on transport of amine storage granules in sympathetic nerves of rat,” Eur. J. Pharmacol.5(1), 111–113 (1968). [CrossRef] [PubMed]
- G. W. Kreutzberg, “Neuronal dynamics and axonal flow. IV. Blockage of intra-axonal enzyme transport by colchicine,” Proc. Natl. Acad. Sci. U.S.A.62(3), 722–728 (1969). [CrossRef] [PubMed]
- J. O. Karlsson and J. Sjöstrand, “The effect of colchicine on the axonal transport of protein in the optic nerve and tract of the rabbit,” Brain Res.13(3), 617–619 (1969). [CrossRef] [PubMed]
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- J. O. Karlsson, H. A. Hansson, and J. Sjöstrand, “Effect of colchicine on axonal transport and morphology of retinal ganglion cells,” Z. Zellforsch. Mikrosk. Anat.115(2), 265–283 (1971). [CrossRef] [PubMed]
- I. G. Morgan, “Intraocular colchicine selectively destroys immature ganglion cells in chicken retina,” Neurosci. Lett.24(3), 255–260 (1981). [CrossRef] [PubMed]
- C. Davidson, W. R. Green, and V. G. Wong, “Retinal atrophy induced by intravitreous colchicine,” Invest. Ophthalmol. Vis. Sci.24(3), 301–311 (1983). [PubMed]
- M. G. Honig and R. I. Hume, “Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures,” J. Cell Biol.103(1), 171–187 (1986). [CrossRef] [PubMed]
- R. D. Lund and S. D. Hauschka, “Transplanted neural tissue develops connections with host rat brain,” Science193(4253), 582–584 (1976). [CrossRef] [PubMed]
- P. W. Land and R. D. Lund, “Development of the rat’s uncrossed retinotectal pathway and its relation to plasticity studies,” Science205(4407), 698–700 (1979). [CrossRef] [PubMed]
- F. Mazzoni, E. Novelli, and E. Strettoi, “Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration,” J. Neurosci.28(52), 14282–14292 (2008). [CrossRef] [PubMed]
- U. C. Dräger and D. H. Hubel, “Topography of visual and somatosensory projections to mouse superior colliculus,” J. Neurophysiol.39(1), 91–101 (1976). [PubMed]
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- L. C. Katz, A. Burkhalter, and W. J. Dreyer, “Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex,” Nature310(5977), 498–500 (1984). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- J. Lu, P. Shiromani, and C. B. Saper, “Retinal input to the sleep-active ventrolateral preoptic nucleus in the rat,” Neuroscience93(1), 209–214 (1999). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- M. M. Black and R. J. Lasek, “Slow components of axonal transport: two cytoskeletal networks,” J. Cell Biol.86(2), 616–623 (1980). [CrossRef] [PubMed]
- J. E. Morgan, “Circulation and axonal transport in the optic nerve,” Eye (Lond.)18(11), 1089–1095 (2004). [CrossRef] [PubMed]
- R. J. Lasek, J. A. Garner, and S. T. Brady, “Axonal transport of the cytoplasmic matrix,” J. Cell Biol.99(1), 212s–221s (1984). [CrossRef] [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
- B. Grafstein and D. S. Forman, “Intracellular transport in neurons,” Physiol. Rev.60(4), 1167–1283 (1980). [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- T. A. Viancour and N. A. Kreiter, “Vesicular fast axonal transport rates in young and old rat axons,” Brain Res.628(1-2), 209–217 (1993). [CrossRef] [PubMed]
- T. Nakata, S. Terada, and N. Hirokawa, “Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons,” J. Cell Biol.140(3), 659–674 (1998). [CrossRef] [PubMed]
- C. Kaether, P. Skehel, and C. G. Dotti, “Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons,” Mol. Biol. Cell11(4), 1213–1224 (2000). [PubMed]
- B. Fortune, G. A. Cull, and C. F. Burgoyne, “Relative course of retinal nerve fiber layer birefringence and thickness and retinal function changes after optic nerve transection,” Invest. Ophthalmol. Vis. Sci.49(10), 4444–4452 (2008). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Microtubules contribute to the birefringence of the retinal nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.46(12), 4588–4593 (2005). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Linear birefringence of the retinal nerve fiber layer measured in vitro with a multispectral imaging micropolarimeter,” J. Biomed. Opt.7(2), 199–204 (2002). [CrossRef] [PubMed]
- Q. Zhou and R. W. Knighton, “Light scattering and form birefringence of parallel cylindrical arrays that represent cellular organelles of the retinal nerve fiber layer,” Appl. Opt.36(10), 2273–2285 (1997). [CrossRef] [PubMed]
- B. A. Sabel, R. Engelmann, and M. F. Humphrey, “In vivo confocal neuroimaging (ICON) of CNS neurons,” Nat. Med.3(2), 244–247 (1997). [CrossRef] [PubMed]
- R. Engelmann and B. A. Sabel, “In vivo imaging of mammalian central nervous system neurons with the in vivo confocal neuroimaging (ICON) method,” Methods Enzymol.307, 563–570 (1999). [CrossRef] [PubMed]
- S. Thanos, L. Indorf, and R. Naskar, “In vivo FM: using conventional fluorescence microscopy to monitor retinal neuronal death in vivo,” Trends Neurosci.25(9), 441–444 (2002). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. S. Leung and R. N. Weinreb, “Experimental detection of retinal ganglion cell damage in vivo,” Exp. Eye Res.88(4), 831–836 (2009). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- M. K. Walsh and H. A. Quigley, “In vivo time-lapse fluorescence imaging of individual retinal ganglion cells in mice,” J. Neurosci. Methods169(1), 214–221 (2008). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- H. A. Quigley and E. M. Addicks, “Chronic experimental glaucoma in primates. II. Effect of extended intraocular pressure elevation on optic nerve head and axonal transport,” Invest. Ophthalmol. Vis. Sci.19(2), 137–152 (1980). [PubMed]
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Rapid axonal transport in primate optic nerve. Distribution of pressure-induced interruption,” Arch. Ophthalmol.99(4), 650–654 (1981). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Reversibility of optic nerve damage in primate eyes subjected to intraocular pressure above systolic blood pressure,” Br. J. Ophthalmol.65(10), 661–672 (1981). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Breakdown of the normal optic nerve head blood-brain barrier following acute elevation of intraocular pressure in experimental animals,” Invest. Ophthalmol. Vis. Sci.19(3), 244–255 (1980). [PubMed]
- R. L. Radius, E. L. Schwartz, and D. R. Anderson, “Failure of unilateral carotid artery ligation to affect pressure-induced interruption of rapid axonal transport in primate optic nerves,” Invest. Ophthalmol. Vis. Sci.19(2), 153–157 (1980). [PubMed]
- H. A. Quigley, J. Guy, and D. R. Anderson, “Blockade of rapid axonal transport. Effect of intraocular pressure elevation in primate optic nerve,” Arch. Ophthalmol.97(3), 525–531 (1979). [CrossRef] [PubMed]
- H. A. Quigley and D. R. Anderson, “Distribution of axonal transport blockade by acute intraocular pressure elevation in the primate optic nerve head,” Invest. Ophthalmol. Vis. Sci.16(7), 640–644 (1977). [PubMed]
- H. Quigley and D. R. Anderson, “The dynamics and location of axonal transport blockade by acute intraocular pressure elevation in primate optic nerve,” Invest. Ophthalmol.15(8), 606–616 (1976). [PubMed]
- D. R. Anderson and A. Hendrickson, “Effect of intraocular pressure on rapid axoplasmic transport in monkey optic nerve,” Invest. Ophthalmol.13(10), 771–783 (1974). [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- A. Angelucci, F. Clascá, and M. Sur, “Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains,” J. Neurosci. Methods65(1), 101–112 (1996). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- A. J. Reynolds, S. E. Bartlett, and I. A. Hendry, “Molecular mechanisms regulating the retrograde axonal transport of neurotrophins,” Brain Res. Brain Res. Rev.33(2-3), 169–178 (2000). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- M. D. Fleming, R. M. Benca, and M. Behan, “Retinal projections to the subcortical visual system in congenic albino and pigmented rats,” Neuroscience143(3), 895–904 (2006). [CrossRef] [PubMed]
- M. D. Fleming, R. M. Benca, and M. Behan, “Retinal projections to the subcortical visual system in congenic albino and pigmented rats,” Neuroscience143(3), 895–904 (2006). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- M. M. Black and R. J. Lasek, “Slow components of axonal transport: two cytoskeletal networks,” J. Cell Biol.86(2), 616–623 (1980). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- R. J. Lasek, J. A. Garner, and S. T. Brady, “Axonal transport of the cytoplasmic matrix,” J. Cell Biol.99(1), 212s–221s (1984). [CrossRef] [PubMed]
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- A. Brown, “Axonal transport of membranous and nonmembranous cargoes: a unified perspective,” J. Cell Biol.160(6), 817–821 (2003). [CrossRef] [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- D. S. Minckler, A. H. Bunt, and I. B. Klock, “Radioautographic and cytochemical ultrastructural studies of axoplasmic transport in the monkey optic nerve head,” Invest. Ophthalmol. Vis. Sci.17(1), 33–50 (1978). [PubMed]
- D. S. Minckler, A. H. Bunt, and G. W. Johanson, “Orthograde and retrograde axoplasmic transport during acute ocular hypertension in the monkey,” Invest. Ophthalmol. Vis. Sci.16(5), 426–441 (1977). [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- B. Fortune, G. A. Cull, and C. F. Burgoyne, “Relative course of retinal nerve fiber layer birefringence and thickness and retinal function changes after optic nerve transection,” Invest. Ophthalmol. Vis. Sci.49(10), 4444–4452 (2008). [CrossRef] [PubMed]
- L. C. Katz, A. Burkhalter, and W. J. Dreyer, “Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex,” Nature310(5977), 498–500 (1984). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- A. Angelucci, F. Clascá, and M. Sur, “Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains,” J. Neurosci. Methods65(1), 101–112 (1996). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- B. Fortune, G. A. Cull, and C. F. Burgoyne, “Relative course of retinal nerve fiber layer birefringence and thickness and retinal function changes after optic nerve transection,” Invest. Ophthalmol. Vis. Sci.49(10), 4444–4452 (2008). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- A. Dahlström, “Effect of colchicine on transport of amine storage granules in sympathetic nerves of rat,” Eur. J. Pharmacol.5(1), 111–113 (1968). [CrossRef] [PubMed]
- L. Dandona, A. Hendrickson, and H. A. Quigley, “Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus,” Invest. Ophthalmol. Vis. Sci.32(5), 1593–1599 (1991). [PubMed]
- C. Davidson, W. R. Green, and V. G. Wong, “Retinal atrophy induced by intravitreous colchicine,” Invest. Ophthalmol. Vis. Sci.24(3), 301–311 (1983). [PubMed]
- S. Reuss and K. Decker, “Anterograde tracing of retinohypothalamic afferents with Fluoro-Gold,” Brain Res.745(1-2), 197–204 (1997). [CrossRef] [PubMed]
- C. Kaether, P. Skehel, and C. G. Dotti, “Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons,” Mol. Biol. Cell11(4), 1213–1224 (2000). [PubMed]
- U. C. Dräger and D. H. Hubel, “Topography of visual and somatosensory projections to mouse superior colliculus,” J. Neurophysiol.39(1), 91–101 (1976). [PubMed]
- L. C. Katz, A. Burkhalter, and W. J. Dreyer, “Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex,” Nature310(5977), 498–500 (1984). [CrossRef] [PubMed]
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- O. J. Eigsti, “A cytological study of colchicine effects in the induction of polyploidy in plants,” Proc. Natl. Acad. Sci. U.S.A.24(2), 56–63 (1938). [CrossRef] [PubMed]
- R. Engelmann and B. A. Sabel, “In vivo imaging of mammalian central nervous system neurons with the in vivo confocal neuroimaging (ICON) method,” Methods Enzymol.307, 563–570 (1999). [CrossRef] [PubMed]
- B. A. Sabel, R. Engelmann, and M. F. Humphrey, “In vivo confocal neuroimaging (ICON) of CNS neurons,” Nat. Med.3(2), 244–247 (1997). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- M. D. Fleming, R. M. Benca, and M. Behan, “Retinal projections to the subcortical visual system in congenic albino and pigmented rats,” Neuroscience143(3), 895–904 (2006). [CrossRef] [PubMed]
- B. Grafstein and D. S. Forman, “Intracellular transport in neurons,” Physiol. Rev.60(4), 1167–1283 (1980). [PubMed]
- P. H. Luppi, P. Fort, and M. Jouvet, “Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons,” Brain Res.534(1-2), 209–224 (1990). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- B. Fortune, G. A. Cull, and C. F. Burgoyne, “Relative course of retinal nerve fiber layer birefringence and thickness and retinal function changes after optic nerve transection,” Invest. Ophthalmol. Vis. Sci.49(10), 4444–4452 (2008). [CrossRef] [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- D. Gaasterland, T. Tanishima, and T. Kuwabara, “Axoplasmic flow during chronic experimental glaucoma. 1. Light and electron microscopic studies of the monkey optic nervehead during development of glaucomatous cupping,” Invest. Ophthalmol. Vis. Sci.17(9), 838–846 (1978). [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- R. J. Lasek, J. A. Garner, and S. T. Brady, “Axonal transport of the cytoplasmic matrix,” J. Cell Biol.99(1), 212s–221s (1984). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- X. C. Wan, J. Q. Trojanowski, and J. O. Gonatas, “Cholera toxin and wheat germ agglutinin conjugates as neuroanatomical probes: their uptake and clearance, transganglionic and retrograde transport and sensitivity,” Brain Res.243(2), 215–224 (1982). [CrossRef] [PubMed]
- J. Q. Trojanowski, J. O. Gonatas, and N. K. Gonatas, “Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP,” Brain Res.231(1), 33–50 (1982). [CrossRef] [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- J. Q. Trojanowski, J. O. Gonatas, and N. K. Gonatas, “Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP,” Brain Res.231(1), 33–50 (1982). [CrossRef] [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
- B. Grafstein and D. S. Forman, “Intracellular transport in neurons,” Physiol. Rev.60(4), 1167–1283 (1980). [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- C. Davidson, W. R. Green, and V. G. Wong, “Retinal atrophy induced by intravitreous colchicine,” Invest. Ophthalmol. Vis. Sci.24(3), 301–311 (1983). [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- H. A. Quigley, J. Guy, and D. R. Anderson, “Blockade of rapid axonal transport. Effect of intraocular pressure elevation in primate optic nerve,” Arch. Ophthalmol.97(3), 525–531 (1979). [CrossRef] [PubMed]
- J. O. Karlsson, H. A. Hansson, and J. Sjöstrand, “Effect of colchicine on axonal transport and morphology of retinal ganglion cells,” Z. Zellforsch. Mikrosk. Anat.115(2), 265–283 (1971). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- R. D. Lund and S. D. Hauschka, “Transplanted neural tissue develops connections with host rat brain,” Science193(4253), 582–584 (1976). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- L. Dandona, A. Hendrickson, and H. A. Quigley, “Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus,” Invest. Ophthalmol. Vis. Sci.32(5), 1593–1599 (1991). [PubMed]
- D. R. Anderson and A. Hendrickson, “Effect of intraocular pressure on rapid axoplasmic transport in monkey optic nerve,” Invest. Ophthalmol.13(10), 771–783 (1974). [PubMed]
- A. J. Reynolds, S. E. Bartlett, and I. A. Hendry, “Molecular mechanisms regulating the retrograde axonal transport of neurotrophins,” Brain Res. Brain Res. Rev.33(2-3), 169–178 (2000). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- M. Hirakawa, J. T. McCabe, and M. Kawata, “Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit,” Cell Tissue Res.267(3), 419–427 (1992). [CrossRef] [PubMed]
- T. Nakata, S. Terada, and N. Hirokawa, “Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons,” J. Cell Biol.140(3), 659–674 (1998). [CrossRef] [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- P. J. Hollenbeck and W. M. Saxton, “The axonal transport of mitochondria,” J. Cell Sci.118(23), 5411–5419 (2005). [CrossRef] [PubMed]
- M. G. Honig and R. I. Hume, “Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures,” J. Cell Biol.103(1), 171–187 (1986). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Microtubules contribute to the birefringence of the retinal nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.46(12), 4588–4593 (2005). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Linear birefringence of the retinal nerve fiber layer measured in vitro with a multispectral imaging micropolarimeter,” J. Biomed. Opt.7(2), 199–204 (2002). [CrossRef] [PubMed]
- U. C. Dräger and D. H. Hubel, “Topography of visual and somatosensory projections to mouse superior colliculus,” J. Neurophysiol.39(1), 91–101 (1976). [PubMed]
- M. G. Honig and R. I. Hume, “Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures,” J. Cell Biol.103(1), 171–187 (1986). [CrossRef] [PubMed]
- B. A. Sabel, R. Engelmann, and M. F. Humphrey, “In vivo confocal neuroimaging (ICON) of CNS neurons,” Nat. Med.3(2), 244–247 (1997). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- S. Thanos, L. Indorf, and R. Naskar, “In vivo FM: using conventional fluorescence microscopy to monitor retinal neuronal death in vivo,” Trends Neurosci.25(9), 441–444 (2002). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- S. Inoue, “The effect of colchicine on the microscopic and submicroscopic structure of the mitotic spindle,” Exp. Cell Res. Suppl.2, 305–318 (1952).
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- D. S. Minckler, A. H. Bunt, and G. W. Johanson, “Orthograde and retrograde axoplasmic transport during acute ocular hypertension in the monkey,” Invest. Ophthalmol. Vis. Sci.16(5), 426–441 (1977). [PubMed]
- J. O. Johansson, “Inhibition and recovery of retrograde axoplasmic transport in rat optic nerve during and after elevated IOP in vivo,” Exp. Eye Res.46(2), 223–227 (1988). [CrossRef] [PubMed]
- J. O. Johansson, “Retrograde axoplasmic transport in rat optic nerve in vivo. What causes blockage at increased intraocular pressure?” Exp. Eye Res.43(4), 653–660 (1986). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
- P. H. Luppi, P. Fort, and M. Jouvet, “Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons,” Brain Res.534(1-2), 209–224 (1990). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- C. Kaether, P. Skehel, and C. G. Dotti, “Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons,” Mol. Biol. Cell11(4), 1213–1224 (2000). [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- J. O. Karlsson, H. A. Hansson, and J. Sjöstrand, “Effect of colchicine on axonal transport and morphology of retinal ganglion cells,” Z. Zellforsch. Mikrosk. Anat.115(2), 265–283 (1971). [CrossRef] [PubMed]
- J. O. Karlsson and J. Sjöstrand, “The effect of colchicine on the axonal transport of protein in the optic nerve and tract of the rabbit,” Brain Res.13(3), 617–619 (1969). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, and H. J. Karten, “The transport rate of cholera toxin B subunit in the retinofugal pathways of the chick,” Neuroscience92(2), 665–676 (1999). [CrossRef] [PubMed]
- L. C. Katz, A. Burkhalter, and W. J. Dreyer, “Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex,” Nature310(5977), 498–500 (1984). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- M. Hirakawa, J. T. McCabe, and M. Kawata, “Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit,” Cell Tissue Res.267(3), 419–427 (1992). [CrossRef] [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
- D. S. Minckler, A. H. Bunt, and I. B. Klock, “Radioautographic and cytochemical ultrastructural studies of axoplasmic transport in the monkey optic nerve head,” Invest. Ophthalmol. Vis. Sci.17(1), 33–50 (1978). [PubMed]
- X. R. Huang and R. W. Knighton, “Microtubules contribute to the birefringence of the retinal nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.46(12), 4588–4593 (2005). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Linear birefringence of the retinal nerve fiber layer measured in vitro with a multispectral imaging micropolarimeter,” J. Biomed. Opt.7(2), 199–204 (2002). [CrossRef] [PubMed]
- Q. Zhou and R. W. Knighton, “Light scattering and form birefringence of parallel cylindrical arrays that represent cellular organelles of the retinal nerve fiber layer,” Appl. Opt.36(10), 2273–2285 (1997). [CrossRef] [PubMed]
- T. A. Viancour and N. A. Kreiter, “Vesicular fast axonal transport rates in young and old rat axons,” Brain Res.628(1-2), 209–217 (1993). [CrossRef] [PubMed]
- G. W. Kreutzberg, “Neuronal dynamics and axonal flow. IV. Blockage of intra-axonal enzyme transport by colchicine,” Proc. Natl. Acad. Sci. U.S.A.62(3), 722–728 (1969). [CrossRef] [PubMed]
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
- D. Gaasterland, T. Tanishima, and T. Kuwabara, “Axoplasmic flow during chronic experimental glaucoma. 1. Light and electron microscopic studies of the monkey optic nervehead during development of glaucomatous cupping,” Invest. Ophthalmol. Vis. Sci.17(9), 838–846 (1978). [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- P. W. Lampert, M. H. Vogel, and L. E. Zimmerman, “Pathology of the optic nerve in experimental acute glaucoma. Electron microscopic studies,” Invest. Ophthalmol.7(2), 199–213 (1968). [PubMed]
- P. W. Land and R. D. Lund, “Development of the rat’s uncrossed retinotectal pathway and its relation to plasticity studies,” Science205(4407), 698–700 (1979). [CrossRef] [PubMed]
- R. J. Lasek, J. A. Garner, and S. T. Brady, “Axonal transport of the cytoplasmic matrix,” J. Cell Biol.99(1), 212s–221s (1984). [CrossRef] [PubMed]
- M. M. Black and R. J. Lasek, “Slow components of axonal transport: two cytoskeletal networks,” J. Cell Biol.86(2), 616–623 (1980). [CrossRef] [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. S. Leung and R. N. Weinreb, “Experimental detection of retinal ganglion cell damage in vivo,” Exp. Eye Res.88(4), 831–836 (2009). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- J. Lu, P. Shiromani, and C. B. Saper, “Retinal input to the sleep-active ventrolateral preoptic nucleus in the rat,” Neuroscience93(1), 209–214 (1999). [CrossRef] [PubMed]
- N. Rivera and N. Lugo, “Four retinal ganglion cell types that project to the superior colliculus in the thirteen-lined ground squirrel (Spermophilus tridecemlineatus),” J. Comp. Neurol.396(1), 105–120 (1998). [CrossRef] [PubMed]
- P. W. Land and R. D. Lund, “Development of the rat’s uncrossed retinotectal pathway and its relation to plasticity studies,” Science205(4407), 698–700 (1979). [CrossRef] [PubMed]
- R. D. Lund and S. D. Hauschka, “Transplanted neural tissue develops connections with host rat brain,” Science193(4253), 582–584 (1976). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- P. H. Luppi, P. Fort, and M. Jouvet, “Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons,” Brain Res.534(1-2), 209–224 (1990). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- F. Mazzoni, E. Novelli, and E. Strettoi, “Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration,” J. Neurosci.28(52), 14282–14292 (2008). [CrossRef] [PubMed]
- M. Hirakawa, J. T. McCabe, and M. Kawata, “Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit,” Cell Tissue Res.267(3), 419–427 (1992). [CrossRef] [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- J. D. Mikkelsen, “Visualization of efferent retinal projections by immunohistochemical identification of cholera toxin subunit B,” Brain Res. Bull.28(4), 619–623 (1992). [CrossRef] [PubMed]
- R. D. Vale and R. A. Milligan, “The way things move: looking under the hood of molecular motor proteins,” Science288(5463), 88–95 (2000). [CrossRef] [PubMed]
- D. S. Minckler, A. H. Bunt, and I. B. Klock, “Radioautographic and cytochemical ultrastructural studies of axoplasmic transport in the monkey optic nerve head,” Invest. Ophthalmol. Vis. Sci.17(1), 33–50 (1978). [PubMed]
- D. S. Minckler, A. H. Bunt, and G. W. Johanson, “Orthograde and retrograde axoplasmic transport during acute ocular hypertension in the monkey,” Invest. Ophthalmol. Vis. Sci.16(5), 426–441 (1977). [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- I. G. Morgan, “Intraocular colchicine selectively destroys immature ganglion cells in chicken retina,” Neurosci. Lett.24(3), 255–260 (1981). [CrossRef] [PubMed]
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
- J. E. Morgan, “Circulation and axonal transport in the optic nerve,” Eye (Lond.)18(11), 1089–1095 (2004). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- T. Nakata, S. Terada, and N. Hirokawa, “Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons,” J. Cell Biol.140(3), 659–674 (1998). [CrossRef] [PubMed]
- S. Thanos, L. Indorf, and R. Naskar, “In vivo FM: using conventional fluorescence microscopy to monitor retinal neuronal death in vivo,” Trends Neurosci.25(9), 441–444 (2002). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- F. Mazzoni, E. Novelli, and E. Strettoi, “Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration,” J. Neurosci.28(52), 14282–14292 (2008). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- S. Ochs, “Fast transport of materials in mammalian nerve fibers,” Science176(4032), 252–260 (1972). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- H. Quigley and D. R. Anderson, “The dynamics and location of axonal transport blockade by acute intraocular pressure elevation in primate optic nerve,” Invest. Ophthalmol.15(8), 606–616 (1976). [PubMed]
- M. K. Walsh and H. A. Quigley, “In vivo time-lapse fluorescence imaging of individual retinal ganglion cells in mice,” J. Neurosci. Methods169(1), 214–221 (2008). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- L. Dandona, A. Hendrickson, and H. A. Quigley, “Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus,” Invest. Ophthalmol. Vis. Sci.32(5), 1593–1599 (1991). [PubMed]
- H. A. Quigley and E. M. Addicks, “Chronic experimental glaucoma in primates. II. Effect of extended intraocular pressure elevation on optic nerve head and axonal transport,” Invest. Ophthalmol. Vis. Sci.19(2), 137–152 (1980). [PubMed]
- H. A. Quigley, J. Guy, and D. R. Anderson, “Blockade of rapid axonal transport. Effect of intraocular pressure elevation in primate optic nerve,” Arch. Ophthalmol.97(3), 525–531 (1979). [CrossRef] [PubMed]
- H. A. Quigley and D. R. Anderson, “Distribution of axonal transport blockade by acute intraocular pressure elevation in the primate optic nerve head,” Invest. Ophthalmol. Vis. Sci.16(7), 640–644 (1977). [PubMed]
- R. L. Radius and D. R. Anderson, “Reversibility of optic nerve damage in primate eyes subjected to intraocular pressure above systolic blood pressure,” Br. J. Ophthalmol.65(10), 661–672 (1981). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Rapid axonal transport in primate optic nerve. Distribution of pressure-induced interruption,” Arch. Ophthalmol.99(4), 650–654 (1981). [CrossRef] [PubMed]
- R. L. Radius, E. L. Schwartz, and D. R. Anderson, “Failure of unilateral carotid artery ligation to affect pressure-induced interruption of rapid axonal transport in primate optic nerves,” Invest. Ophthalmol. Vis. Sci.19(2), 153–157 (1980). [PubMed]
- R. L. Radius and D. R. Anderson, “Breakdown of the normal optic nerve head blood-brain barrier following acute elevation of intraocular pressure in experimental animals,” Invest. Ophthalmol. Vis. Sci.19(3), 244–255 (1980). [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- S. Reuss and K. Decker, “Anterograde tracing of retinohypothalamic afferents with Fluoro-Gold,” Brain Res.745(1-2), 197–204 (1997). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- A. J. Reynolds, S. E. Bartlett, and I. A. Hendry, “Molecular mechanisms regulating the retrograde axonal transport of neurotrophins,” Brain Res. Brain Res. Rev.33(2-3), 169–178 (2000). [CrossRef] [PubMed]
- N. Rivera and N. Lugo, “Four retinal ganglion cell types that project to the superior colliculus in the thirteen-lined ground squirrel (Spermophilus tridecemlineatus),” J. Comp. Neurol.396(1), 105–120 (1998). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, and H. J. Karten, “The transport rate of cholera toxin B subunit in the retinofugal pathways of the chick,” Neuroscience92(2), 665–676 (1999). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- R. Engelmann and B. A. Sabel, “In vivo imaging of mammalian central nervous system neurons with the in vivo confocal neuroimaging (ICON) method,” Methods Enzymol.307, 563–570 (1999). [CrossRef] [PubMed]
- B. A. Sabel, R. Engelmann, and M. F. Humphrey, “In vivo confocal neuroimaging (ICON) of CNS neurons,” Nat. Med.3(2), 244–247 (1997). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- J. Lu, P. Shiromani, and C. B. Saper, “Retinal input to the sleep-active ventrolateral preoptic nucleus in the rat,” Neuroscience93(1), 209–214 (1999). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- P. J. Hollenbeck and W. M. Saxton, “The axonal transport of mitochondria,” J. Cell Sci.118(23), 5411–5419 (2005). [CrossRef] [PubMed]
- M. E. Schwab and H. Thoenen, “Retrograde axonal and transsynaptic transport of macromolecules: physiological and pathophysiological importance,” Agents Actions7(3), 361–368 (1977). [CrossRef] [PubMed]
- R. L. Radius, E. L. Schwartz, and D. R. Anderson, “Failure of unilateral carotid artery ligation to affect pressure-induced interruption of rapid axonal transport in primate optic nerves,” Invest. Ophthalmol. Vis. Sci.19(2), 153–157 (1980). [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- J. Lu, P. Shiromani, and C. B. Saper, “Retinal input to the sleep-active ventrolateral preoptic nucleus in the rat,” Neuroscience93(1), 209–214 (1999). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- J. O. Karlsson, H. A. Hansson, and J. Sjöstrand, “Effect of colchicine on axonal transport and morphology of retinal ganglion cells,” Z. Zellforsch. Mikrosk. Anat.115(2), 265–283 (1971). [CrossRef] [PubMed]
- J. O. Karlsson and J. Sjöstrand, “The effect of colchicine on the axonal transport of protein in the optic nerve and tract of the rabbit,” Brain Res.13(3), 617–619 (1969). [CrossRef] [PubMed]
- C. Kaether, P. Skehel, and C. G. Dotti, “Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons,” Mol. Biol. Cell11(4), 1213–1224 (2000). [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
- F. Mazzoni, E. Novelli, and E. Strettoi, “Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration,” J. Neurosci.28(52), 14282–14292 (2008). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- A. Angelucci, F. Clascá, and M. Sur, “Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains,” J. Neurosci. Methods65(1), 101–112 (1996). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- D. Gaasterland, T. Tanishima, and T. Kuwabara, “Axoplasmic flow during chronic experimental glaucoma. 1. Light and electron microscopic studies of the monkey optic nervehead during development of glaucomatous cupping,” Invest. Ophthalmol. Vis. Sci.17(9), 838–846 (1978). [PubMed]
- T. Nakata, S. Terada, and N. Hirokawa, “Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons,” J. Cell Biol.140(3), 659–674 (1998). [CrossRef] [PubMed]
- S. Thanos, L. Indorf, and R. Naskar, “In vivo FM: using conventional fluorescence microscopy to monitor retinal neuronal death in vivo,” Trends Neurosci.25(9), 441–444 (2002). [CrossRef] [PubMed]
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- M. E. Schwab and H. Thoenen, “Retrograde axonal and transsynaptic transport of macromolecules: physiological and pathophysiological importance,” Agents Actions7(3), 361–368 (1977). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
- X. C. Wan, J. Q. Trojanowski, and J. O. Gonatas, “Cholera toxin and wheat germ agglutinin conjugates as neuroanatomical probes: their uptake and clearance, transganglionic and retrograde transport and sensitivity,” Brain Res.243(2), 215–224 (1982). [CrossRef] [PubMed]
- J. Q. Trojanowski, J. O. Gonatas, and N. K. Gonatas, “Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP,” Brain Res.231(1), 33–50 (1982). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
- R. D. Vale and R. A. Milligan, “The way things move: looking under the hood of molecular motor proteins,” Science288(5463), 88–95 (2000). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- T. A. Viancour and N. A. Kreiter, “Vesicular fast axonal transport rates in young and old rat axons,” Brain Res.628(1-2), 209–217 (1993). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
- P. W. Lampert, M. H. Vogel, and L. E. Zimmerman, “Pathology of the optic nerve in experimental acute glaucoma. Electron microscopic studies,” Invest. Ophthalmol.7(2), 199–213 (1968). [PubMed]
- M. K. Walsh and H. A. Quigley, “In vivo time-lapse fluorescence imaging of individual retinal ganglion cells in mice,” J. Neurosci. Methods169(1), 214–221 (2008). [CrossRef] [PubMed]
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- X. C. Wan, J. Q. Trojanowski, and J. O. Gonatas, “Cholera toxin and wheat germ agglutinin conjugates as neuroanatomical probes: their uptake and clearance, transganglionic and retrograde transport and sensitivity,” Brain Res.243(2), 215–224 (1982). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- C. K. S. Leung and R. N. Weinreb, “Experimental detection of retinal ganglion cell damage in vivo,” Exp. Eye Res.88(4), 831–836 (2009). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- C. Davidson, W. R. Green, and V. G. Wong, “Retinal atrophy induced by intravitreous colchicine,” Invest. Ophthalmol. Vis. Sci.24(3), 301–311 (1983). [PubMed]
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, and H. J. Karten, “The transport rate of cholera toxin B subunit in the retinofugal pathways of the chick,” Neuroscience92(2), 665–676 (1999). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- P. W. Lampert, M. H. Vogel, and L. E. Zimmerman, “Pathology of the optic nerve in experimental acute glaucoma. Electron microscopic studies,” Invest. Ophthalmol.7(2), 199–213 (1968). [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
Acta Neuropathol.
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
Agents Actions
- M. E. Schwab and H. Thoenen, “Retrograde axonal and transsynaptic transport of macromolecules: physiological and pathophysiological importance,” Agents Actions7(3), 361–368 (1977). [CrossRef] [PubMed]
Appl. Opt.
- Q. Zhou and R. W. Knighton, “Light scattering and form birefringence of parallel cylindrical arrays that represent cellular organelles of the retinal nerve fiber layer,” Appl. Opt.36(10), 2273–2285 (1997). [CrossRef] [PubMed]
Arch. Ophthalmol.
- R. L. Radius and D. R. Anderson, “Rapid axonal transport in primate optic nerve. Distribution of pressure-induced interruption,” Arch. Ophthalmol.99(4), 650–654 (1981). [CrossRef] [PubMed]
- H. A. Quigley, J. Guy, and D. R. Anderson, “Blockade of rapid axonal transport. Effect of intraocular pressure elevation in primate optic nerve,” Arch. Ophthalmol.97(3), 525–531 (1979). [CrossRef] [PubMed]
Biochem. J.
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
Biomed. Opt. Express
- Y. Geng, A. Dubra, L. Yin, W. H. Merigan, R. Sharma, R. T. Libby, and D. R. Williams, “Adaptive optics retinal imaging in the living mouse eye,” Biomed. Opt. Express3(4), 715–734 (2012). [CrossRef] [PubMed]
Br. J. Ophthalmol.
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Reversibility of optic nerve damage in primate eyes subjected to intraocular pressure above systolic blood pressure,” Br. J. Ophthalmol.65(10), 661–672 (1981). [CrossRef] [PubMed]
Brain Res.
- S. Reuss and K. Decker, “Anterograde tracing of retinohypothalamic afferents with Fluoro-Gold,” Brain Res.745(1-2), 197–204 (1997). [CrossRef] [PubMed]
- X. C. Wan, J. Q. Trojanowski, and J. O. Gonatas, “Cholera toxin and wheat germ agglutinin conjugates as neuroanatomical probes: their uptake and clearance, transganglionic and retrograde transport and sensitivity,” Brain Res.243(2), 215–224 (1982). [CrossRef] [PubMed]
- J. Q. Trojanowski, J. O. Gonatas, and N. K. Gonatas, “Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP,” Brain Res.231(1), 33–50 (1982). [CrossRef] [PubMed]
- P. H. Luppi, P. Fort, and M. Jouvet, “Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons,” Brain Res.534(1-2), 209–224 (1990). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- J. O. Karlsson and J. Sjöstrand, “The effect of colchicine on the axonal transport of protein in the optic nerve and tract of the rabbit,” Brain Res.13(3), 617–619 (1969). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- T. A. Viancour and N. A. Kreiter, “Vesicular fast axonal transport rates in young and old rat axons,” Brain Res.628(1-2), 209–217 (1993). [CrossRef] [PubMed]
Brain Res. Brain Res. Rev.
- A. J. Reynolds, S. E. Bartlett, and I. A. Hendry, “Molecular mechanisms regulating the retrograde axonal transport of neurotrophins,” Brain Res. Brain Res. Rev.33(2-3), 169–178 (2000). [CrossRef] [PubMed]
Brain Res. Bull.
- J. D. Mikkelsen, “Visualization of efferent retinal projections by immunohistochemical identification of cholera toxin subunit B,” Brain Res. Bull.28(4), 619–623 (1992). [CrossRef] [PubMed]
Cell Death Dis
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
Cell Tissue Res.
- M. Hirakawa, J. T. McCabe, and M. Kawata, “Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit,” Cell Tissue Res.267(3), 419–427 (1992). [CrossRef] [PubMed]
Eur. J. Pharmacol.
- A. Dahlström, “Effect of colchicine on transport of amine storage granules in sympathetic nerves of rat,” Eur. J. Pharmacol.5(1), 111–113 (1968). [CrossRef] [PubMed]
Exp. Cell Res. Suppl.
- S. Inoue, “The effect of colchicine on the microscopic and submicroscopic structure of the mitotic spindle,” Exp. Cell Res. Suppl.2, 305–318 (1952).
Exp. Eye Res.
- J. O. Johansson, “Retrograde axoplasmic transport in rat optic nerve in vivo. What causes blockage at increased intraocular pressure?” Exp. Eye Res.43(4), 653–660 (1986). [CrossRef] [PubMed]
- J. O. Johansson, “Inhibition and recovery of retrograde axoplasmic transport in rat optic nerve during and after elevated IOP in vivo,” Exp. Eye Res.46(2), 223–227 (1988). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- C. K. S. Leung and R. N. Weinreb, “Experimental detection of retinal ganglion cell damage in vivo,” Exp. Eye Res.88(4), 831–836 (2009). [CrossRef] [PubMed]
Exp. Neurol.
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
Eye (Lond.)
- J. E. Morgan, “Circulation and axonal transport in the optic nerve,” Eye (Lond.)18(11), 1089–1095 (2004). [CrossRef] [PubMed]
Invest. Ophthalmol.
- D. R. Anderson and A. Hendrickson, “Effect of intraocular pressure on rapid axoplasmic transport in monkey optic nerve,” Invest. Ophthalmol.13(10), 771–783 (1974). [PubMed]
- H. Quigley and D. R. Anderson, “The dynamics and location of axonal transport blockade by acute intraocular pressure elevation in primate optic nerve,” Invest. Ophthalmol.15(8), 606–616 (1976). [PubMed]
- P. W. Lampert, M. H. Vogel, and L. E. Zimmerman, “Pathology of the optic nerve in experimental acute glaucoma. Electron microscopic studies,” Invest. Ophthalmol.7(2), 199–213 (1968). [PubMed]
Invest. Ophthalmol. Vis. Sci.
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Breakdown of the normal optic nerve head blood-brain barrier following acute elevation of intraocular pressure in experimental animals,” Invest. Ophthalmol. Vis. Sci.19(3), 244–255 (1980). [PubMed]
- H. A. Quigley and D. R. Anderson, “Distribution of axonal transport blockade by acute intraocular pressure elevation in the primate optic nerve head,” Invest. Ophthalmol. Vis. Sci.16(7), 640–644 (1977). [PubMed]
- R. L. Radius, E. L. Schwartz, and D. R. Anderson, “Failure of unilateral carotid artery ligation to affect pressure-induced interruption of rapid axonal transport in primate optic nerves,” Invest. Ophthalmol. Vis. Sci.19(2), 153–157 (1980). [PubMed]
- D. S. Minckler, A. H. Bunt, and G. W. Johanson, “Orthograde and retrograde axoplasmic transport during acute ocular hypertension in the monkey,” Invest. Ophthalmol. Vis. Sci.16(5), 426–441 (1977). [PubMed]
- D. S. Minckler, A. H. Bunt, and I. B. Klock, “Radioautographic and cytochemical ultrastructural studies of axoplasmic transport in the monkey optic nerve head,” Invest. Ophthalmol. Vis. Sci.17(1), 33–50 (1978). [PubMed]
- D. Gaasterland, T. Tanishima, and T. Kuwabara, “Axoplasmic flow during chronic experimental glaucoma. 1. Light and electron microscopic studies of the monkey optic nervehead during development of glaucomatous cupping,” Invest. Ophthalmol. Vis. Sci.17(9), 838–846 (1978). [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- H. A. Quigley and E. M. Addicks, “Chronic experimental glaucoma in primates. II. Effect of extended intraocular pressure elevation on optic nerve head and axonal transport,” Invest. Ophthalmol. Vis. Sci.19(2), 137–152 (1980). [PubMed]
- L. Dandona, A. Hendrickson, and H. A. Quigley, “Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus,” Invest. Ophthalmol. Vis. Sci.32(5), 1593–1599 (1991). [PubMed]
- C. Davidson, W. R. Green, and V. G. Wong, “Retinal atrophy induced by intravitreous colchicine,” Invest. Ophthalmol. Vis. Sci.24(3), 301–311 (1983). [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- B. Fortune, G. A. Cull, and C. F. Burgoyne, “Relative course of retinal nerve fiber layer birefringence and thickness and retinal function changes after optic nerve transection,” Invest. Ophthalmol. Vis. Sci.49(10), 4444–4452 (2008). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Microtubules contribute to the birefringence of the retinal nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.46(12), 4588–4593 (2005). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
J. Biomed. Opt.
- X. R. Huang and R. W. Knighton, “Linear birefringence of the retinal nerve fiber layer measured in vitro with a multispectral imaging micropolarimeter,” J. Biomed. Opt.7(2), 199–204 (2002). [CrossRef] [PubMed]
J. Cell Biol.
- R. J. Lasek, J. A. Garner, and S. T. Brady, “Axonal transport of the cytoplasmic matrix,” J. Cell Biol.99(1), 212s–221s (1984). [CrossRef] [PubMed]
- T. Nakata, S. Terada, and N. Hirokawa, “Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons,” J. Cell Biol.140(3), 659–674 (1998). [CrossRef] [PubMed]
- M. M. Black and R. J. Lasek, “Slow components of axonal transport: two cytoskeletal networks,” J. Cell Biol.86(2), 616–623 (1980). [CrossRef] [PubMed]
- M. G. Honig and R. I. Hume, “Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures,” J. Cell Biol.103(1), 171–187 (1986). [CrossRef] [PubMed]
- A. Brown, “Axonal transport of membranous and nonmembranous cargoes: a unified perspective,” J. Cell Biol.160(6), 817–821 (2003). [CrossRef] [PubMed]
J. Cell Sci.
- P. J. Hollenbeck and W. M. Saxton, “The axonal transport of mitochondria,” J. Cell Sci.118(23), 5411–5419 (2005). [CrossRef] [PubMed]
J. Clin. Invest.
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
J. Comp. Neurol.
- N. Rivera and N. Lugo, “Four retinal ganglion cell types that project to the superior colliculus in the thirteen-lined ground squirrel (Spermophilus tridecemlineatus),” J. Comp. Neurol.396(1), 105–120 (1998). [CrossRef] [PubMed]
J. Neurochem.
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
J. Neurophysiol.
- U. C. Dräger and D. H. Hubel, “Topography of visual and somatosensory projections to mouse superior colliculus,” J. Neurophysiol.39(1), 91–101 (1976). [PubMed]
J. Neurosci.
- F. Mazzoni, E. Novelli, and E. Strettoi, “Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration,” J. Neurosci.28(52), 14282–14292 (2008). [CrossRef] [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
J. Neurosci. Methods
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- A. Angelucci, F. Clascá, and M. Sur, “Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains,” J. Neurosci. Methods65(1), 101–112 (1996). [CrossRef] [PubMed]
- M. K. Walsh and H. A. Quigley, “In vivo time-lapse fluorescence imaging of individual retinal ganglion cells in mice,” J. Neurosci. Methods169(1), 214–221 (2008). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
Methods Enzymol.
- R. Engelmann and B. A. Sabel, “In vivo imaging of mammalian central nervous system neurons with the in vivo confocal neuroimaging (ICON) method,” Methods Enzymol.307, 563–570 (1999). [CrossRef] [PubMed]
Mol. Biol. Cell
- C. Kaether, P. Skehel, and C. G. Dotti, “Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons,” Mol. Biol. Cell11(4), 1213–1224 (2000). [PubMed]
Mol. Cell. Biol.
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
Nat. Cell Biol.
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
Nat. Med.
- B. A. Sabel, R. Engelmann, and M. F. Humphrey, “In vivo confocal neuroimaging (ICON) of CNS neurons,” Nat. Med.3(2), 244–247 (1997). [CrossRef] [PubMed]
Nat. Methods
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
Nature
- L. C. Katz, A. Burkhalter, and W. J. Dreyer, “Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex,” Nature310(5977), 498–500 (1984). [CrossRef] [PubMed]
Neuroimage
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
Neurology
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
Neurosci. Lett.
- I. G. Morgan, “Intraocular colchicine selectively destroys immature ganglion cells in chicken retina,” Neurosci. Lett.24(3), 255–260 (1981). [CrossRef] [PubMed]
Neuroscience
- J. Lu, P. Shiromani, and C. B. Saper, “Retinal input to the sleep-active ventrolateral preoptic nucleus in the rat,” Neuroscience93(1), 209–214 (1999). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, and H. J. Karten, “The transport rate of cholera toxin B subunit in the retinofugal pathways of the chick,” Neuroscience92(2), 665–676 (1999). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- M. D. Fleming, R. M. Benca, and M. Behan, “Retinal projections to the subcortical visual system in congenic albino and pigmented rats,” Neuroscience143(3), 895–904 (2006). [CrossRef] [PubMed]
Opt. Express
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
Physiol. Rev.
- B. Grafstein and D. S. Forman, “Intracellular transport in neurons,” Physiol. Rev.60(4), 1167–1283 (1980). [PubMed]
Proc. Natl. Acad. Sci. U.S.A.
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- O. J. Eigsti, “A cytological study of colchicine effects in the induction of polyploidy in plants,” Proc. Natl. Acad. Sci. U.S.A.24(2), 56–63 (1938). [CrossRef] [PubMed]
- G. W. Kreutzberg, “Neuronal dynamics and axonal flow. IV. Blockage of intra-axonal enzyme transport by colchicine,” Proc. Natl. Acad. Sci. U.S.A.62(3), 722–728 (1969). [CrossRef] [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
Science
- S. Ochs, “Fast transport of materials in mammalian nerve fibers,” Science176(4032), 252–260 (1972). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- R. D. Lund and S. D. Hauschka, “Transplanted neural tissue develops connections with host rat brain,” Science193(4253), 582–584 (1976). [CrossRef] [PubMed]
- P. W. Land and R. D. Lund, “Development of the rat’s uncrossed retinotectal pathway and its relation to plasticity studies,” Science205(4407), 698–700 (1979). [CrossRef] [PubMed]
- R. D. Vale and R. A. Milligan, “The way things move: looking under the hood of molecular motor proteins,” Science288(5463), 88–95 (2000). [CrossRef] [PubMed]
Trends Neurosci.
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- S. Thanos, L. Indorf, and R. Naskar, “In vivo FM: using conventional fluorescence microscopy to monitor retinal neuronal death in vivo,” Trends Neurosci.25(9), 441–444 (2002). [CrossRef] [PubMed]
Z. Zellforsch. Mikrosk. Anat.
- J. O. Karlsson, H. A. Hansson, and J. Sjöstrand, “Effect of colchicine on axonal transport and morphology of retinal ganglion cells,” Z. Zellforsch. Mikrosk. Anat.115(2), 265–283 (1971). [CrossRef] [PubMed]
Other
- O. J. Eigsti and P. D. Dustin, Jr., Colchicine— in Agriculture, Medicine, Biology and Chemistry (Iowa State College Press, Ames, IA, 1955)
2012, Howell, J. Clin. Invest.
- G. R. Howell, I. Soto, X. Zhu, M. Ryan, D. G. Macalinao, G. L. Sousa, L. B. Caddle, K. H. MacNicoll, J. M. Barbay, V. Porciatti, M. G. Anderson, R. S. Smith, A. F. Clark, R. T. Libby, and S. W. John, “Radiation treatment inhibits monocyte entry into the optic nerve head and prevents neuronal damage in a mouse model of glaucoma,” J. Clin. Invest.122(4), 1246–1261 (2012). [CrossRef] [PubMed]
- B. Fortune, C. F. Burgoyne, G. A. Cull, J. Reynaud, and L. Wang, “Structural and functional abnormalities of retinal ganglion cells measured in vivo at the onset of optic nerve head surface change in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.53(7), 3939–3950 (2012). [CrossRef] [PubMed]
- J. J. Gallagher, X. Zhang, G. J. Ziomek, R. E. Jacobs, and E. L. Bearer, “Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI,” Neuroimage60(3), 1856–1866 (2012). [CrossRef] [PubMed]
- C. K. Leung, R. N. Weinreb, Z. W. Li, S. Liu, J. D. Lindsey, N. Choi, L. Liu, C. Y. Cheung, C. Ye, K. Qiu, L. J. Chen, W. H. Yung, J. G. Crowston, M. Pu, K. F. So, C. P. Pang, and D. S. Lam, “Long-term in vivo imaging and measurement of dendritic shrinkage of retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.52(3), 1539–1547 (2011). [CrossRef] [PubMed]
- G. Chidlow, A. Ebneter, J. P. M. Wood, and R. J. Casson, “The optic nerve head is the site of axonal transport disruption, axonal cytoskeleton damage and putative axonal regeneration failure in a rat model of glaucoma,” Acta Neuropathol.121(6), 737–751 (2011). [CrossRef] [PubMed]
- Y. Takihara, M. Inatani, H. Hayashi, N. Adachi, K. Iwao, T. Inoue, M. Iwao, and H. Tanihara, “Dynamic imaging of axonal transport in living retinal ganglion cells in vitro,” Invest. Ophthalmol. Vis. Sci.52(6), 3039–3045 (2011). [CrossRef] [PubMed]
- S. D. Crish, R. M. Sappington, D. M. Inman, P. J. Horner, and D. J. Calkins, “Distal axonopathy with structural persistence in glaucomatous neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.107(11), 5196–5201 (2010). [CrossRef] [PubMed]
- M. Salinas-Navarro, L. Alarcón-Martínez, F. J. Valiente-Soriano, M. Jiménez-López, S. Mayor-Torroglosa, M. Avilés-Trigueros, M. P. Villegas-Pérez, and M. Vidal-Sanz, “Ocular hypertension impairs optic nerve axonal transport leading to progressive retinal ganglion cell degeneration,” Exp. Eye Res.90(1), 168–183 (2010). [CrossRef] [PubMed]
- Y. Munemasa, Y. Kitaoka, J. Kuribayashi, and S. Ueno, “Modulation of mitochondria in the axon and soma of retinal ganglion cells in a rat glaucoma model,” J. Neurochem.115(6), 1508–1519 (2010). [CrossRef] [PubMed]
- A. Kanamori, M. M. Catrinescu, M. Traistaru, R. Beaubien, and L. A. Levin, “In vivo imaging of retinal ganglion cell axons within the nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.51(4), 2011–2018 (2010). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, K. M. Coxon, J. Duggan, S. Nizari, E. M. Normando, S. L. Sensi, A. M. Sillito, F. W. Fitzke, T. E. Salt, and S. E. Moss, “Imaging multiple phases of neurodegeneration: a novel approach to assessing cell death in vivo,” Cell Death Dis1(1), e3 (2010). [CrossRef] [PubMed]
- C. K. S. Leung and R. N. Weinreb, “Experimental detection of retinal ganglion cell damage in vivo,” Exp. Eye Res.88(4), 831–836 (2009). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, L. Chen, Q. Liu, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage assessed with blue-light confocal scanning laser ophthalmoscopy after ischaemic reperfusion injury,” Br. J. Ophthalmol.93(7), 964–968 (2009). [CrossRef] [PubMed]
- Y. Geng, K. P. Greenberg, R. Wolfe, D. C. Gray, J. J. Hunter, A. Dubra, J. G. Flannery, D. R. Williams, and J. Porter, “In vivo imaging of microscopic structures in the rat retina,” Invest. Ophthalmol. Vis. Sci.50(12), 5872–5879 (2009). [CrossRef] [PubMed]
- G. C. Walter, R. J. Phillips, E. A. Baronowsky, and T. L. Powley, “Versatile, high-resolution anterograde labeling of vagal efferent projections with dextran amines,” J. Neurosci. Methods178(1), 1–9 (2009). [CrossRef] [PubMed]
- F. Mazzoni, E. Novelli, and E. Strettoi, “Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration,” J. Neurosci.28(52), 14282–14292 (2008). [CrossRef] [PubMed]
- B. Fortune, L. Wang, G. Cull, and G. A. Cioffi, “Intravitreal colchicine causes decreased RNFL birefringence without altering RNFL thickness,” Invest. Ophthalmol. Vis. Sci.49(1), 255–261 (2008). [CrossRef] [PubMed]
- I. Soto, E. Oglesby, B. P. Buckingham, J. L. Son, E. D. O. Roberson, M. R. Steele, D. M. Inman, M. L. Vetter, P. J. Horner, and N. Marsh-Armstrong, “Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model,” J. Neurosci.28(2), 548–561 (2008). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, L. Ye, C. McKnight, S. J. Cringle, and D. Y. Yu, “Elevated pressure induced astrocyte damage in the optic nerve,” Brain Res.1244, 142–154 (2008). [CrossRef] [PubMed]
- C. K. S. Leung, J. D. Lindsey, J. G. Crowston, W. K. Ju, Q. Liu, D. U. Bartsch, and R. N. Weinreb, “In vivo imaging of murine retinal ganglion cells,” J. Neurosci. Methods168(2), 475–478 (2008). [CrossRef] [PubMed]
- C. K. Leung, J. D. Lindsey, J. G. Crowston, C. Lijia, S. Chiang, and R. N. Weinreb, “Longitudinal profile of retinal ganglion cell damage after optic nerve crush with blue-light confocal scanning laser ophthalmoscopy,” Invest. Ophthalmol. Vis. Sci.49(11), 4898–4902 (2008). [CrossRef] [PubMed]
- D. C. Gray, R. Wolfe, B. P. Gee, D. Scoles, Y. Geng, B. D. Masella, A. Dubra, S. Luque, D. R. Williams, and W. H. Merigan, “In vivo imaging of the fine structure of rhodamine-labeled macaque retinal ganglion cells,” Invest. Ophthalmol. Vis. Sci.49(1), 467–473 (2008). [CrossRef] [PubMed]
- H. Murata, M. Aihara, Y. N. Chen, T. Ota, J. Numaga, and M. Araie, “Imaging mouse retinal ganglion cells and their loss in vivo by a fundus camera in the normal and ischemia-reperfusion model,” Invest. Ophthalmol. Vis. Sci.49(12), 5546–5552 (2008). [CrossRef] [PubMed]
- M. K. Walsh and H. A. Quigley, “In vivo time-lapse fluorescence imaging of individual retinal ganglion cells in mice,” J. Neurosci. Methods169(1), 214–221 (2008). [CrossRef] [PubMed]
- B. Fortune, G. A. Cull, and C. F. Burgoyne, “Relative course of retinal nerve fiber layer birefringence and thickness and retinal function changes after optic nerve transection,” Invest. Ophthalmol. Vis. Sci.49(10), 4444–4452 (2008). [CrossRef] [PubMed]
- E. L. Bearer, T. L. Falzone, X. W. Zhang, O. Biris, A. Rasin, and R. E. Jacobs, “Role of neuronal activity and kinesin on tract tracing by manganese-enhanced MRI (MEMRI),” Neuroimage37(Suppl 1), S37–S46 (2007). [CrossRef] [PubMed]
- C. Balaratnasingam, W. H. Morgan, L. Bass, G. Matich, S. J. Cringle, and D. Y. Yu, “Axonal transport and cytoskeletal changes in the laminar regions after elevated intraocular pressure,” Invest. Ophthalmol. Vis. Sci.48(8), 3632–3644 (2007). [CrossRef] [PubMed]
- T. Misgeld, M. Kerschensteiner, F. M. Bareyre, R. W. Burgess, and J. W. Lichtman, “Imaging axonal transport of mitochondria in vivo,” Nat. Methods4(7), 559–561 (2007). [CrossRef] [PubMed]
- K. R. G. Martin, H. A. Quigley, D. Valenta, J. Kielczewski, and M. E. Pease, “Optic nerve dynein motor protein distribution changes with intraocular pressure elevation in a rat model of glaucoma,” Exp. Eye Res.83(2), 255–262 (2006). [CrossRef] [PubMed]
- M. D. Fleming, R. M. Benca, and M. Behan, “Retinal projections to the subcortical visual system in congenic albino and pigmented rats,” Neuroscience143(3), 895–904 (2006). [CrossRef] [PubMed]
- D. C. Gray, W. Merigan, J. I. Wolfing, B. P. Gee, J. Porter, A. Dubra, T. H. Twietmeyer, K. Ahamd, R. Tumbar, F. Reinholz, and D. R. Williams, “In vivo fluorescence imaging of primate retinal ganglion cells and retinal pigment epithelial cells,” Opt. Express14(16), 7144–7158 (2006). [CrossRef] [PubMed]
- T. Higashide, I. Kawaguchi, S. Ohkubo, H. Takeda, and K. Sugiyama, “In vivo imaging and counting of rat retinal ganglion cells using a scanning laser ophthalmoscope,” Invest. Ophthalmol. Vis. Sci.47(7), 2943–2950 (2006). [CrossRef] [PubMed]
- L. Guo, T. E. Salt, A. Maass, V. Luong, S. E. Moss, F. W. Fitzke, and M. F. Cordeiro, “Assessment of neuroprotective effects of glutamate modulation on glaucoma-related retinal ganglion cell apoptosis in vivo,” Invest. Ophthalmol. Vis. Sci.47(2), 626–633 (2006). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Microtubules contribute to the birefringence of the retinal nerve fiber layer,” Invest. Ophthalmol. Vis. Sci.46(12), 4588–4593 (2005). [CrossRef] [PubMed]
- S. Roy, B. Zhang, V. M. Lee, and J. Q. Trojanowski, “Axonal transport defects: a common theme in neurodegenerative diseases,” Acta Neuropathol.109(1), 5–13 (2005). [CrossRef] [PubMed]
- P. J. Hollenbeck and W. M. Saxton, “The axonal transport of mitochondria,” J. Cell Sci.118(23), 5411–5419 (2005). [CrossRef] [PubMed]
- J. E. Morgan, “Circulation and axonal transport in the optic nerve,” Eye (Lond.)18(11), 1089–1095 (2004). [CrossRef] [PubMed]
- M. F. Cordeiro, L. Guo, V. Luong, G. Harding, W. Wang, H. E. Jones, S. E. Moss, A. M. Sillito, and F. W. Fitzke, “Real-time imaging of single nerve cell apoptosis in retinal neurodegeneration,” Proc. Natl. Acad. Sci. U.S.A.101(36), 13352–13356 (2004). [CrossRef] [PubMed]
- A. Brown, “Axonal transport of membranous and nonmembranous cargoes: a unified perspective,” J. Cell Biol.160(6), 817–821 (2003). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, R. T. Nguyen, and H. J. Karten, “Tracing developing pathways in the brain: a comparison of carbocyanine dyes and cholera toxin b subunit,” Neuroscience117(4), 831–845 (2003). [CrossRef] [PubMed]
- X. R. Huang and R. W. Knighton, “Linear birefringence of the retinal nerve fiber layer measured in vitro with a multispectral imaging micropolarimeter,” J. Biomed. Opt.7(2), 199–204 (2002). [CrossRef] [PubMed]
- S. Thanos, L. Indorf, and R. Naskar, “In vivo FM: using conventional fluorescence microscopy to monitor retinal neuronal death in vivo,” Trends Neurosci.25(9), 441–444 (2002). [CrossRef] [PubMed]
- C. Kaether, P. Skehel, and C. G. Dotti, “Axonal membrane proteins are transported in distinct carriers: a two-color video microscopy study in cultured hippocampal neurons,” Mol. Biol. Cell11(4), 1213–1224 (2000). [PubMed]
- R. D. Vale and R. A. Milligan, “The way things move: looking under the hood of molecular motor proteins,” Science288(5463), 88–95 (2000). [CrossRef] [PubMed]
- A. J. Reynolds, S. E. Bartlett, and I. A. Hendry, “Molecular mechanisms regulating the retrograde axonal transport of neurotrophins,” Brain Res. Brain Res. Rev.33(2-3), 169–178 (2000). [CrossRef] [PubMed]
- H. A. Quigley, S. J. McKinnon, D. J. Zack, M. E. Pease, L. A. Kerrigan-Baumrind, D. F. Kerrigan, and R. S. Mitchell, “Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats,” Invest. Ophthalmol. Vis. Sci.41(11), 3460–3466 (2000). [PubMed]
- M. E. Pease, S. J. McKinnon, H. A. Quigley, L. A. Kerrigan-Baumrind, and D. J. Zack, “Obstructed axonal transport of BDNF and its receptor TrkB in experimental glaucoma,” Invest. Ophthalmol. Vis. Sci.41(3), 764–774 (2000). [PubMed]
- S. Roy, P. Coffee, G. Smith, R. K. Liem, S. T. Brady, and M. M. Black, “Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport,” J. Neurosci.20(18), 6849–6861 (2000). [PubMed]
- L. Wang, C. L. Ho, D. Sun, R. K. H. Liem, and A. Brown, “Rapid movement of axonal neurofilaments interrupted by prolonged pauses,” Nat. Cell Biol.2(3), 137–141 (2000). [CrossRef] [PubMed]
- J. Lu, P. Shiromani, and C. B. Saper, “Retinal input to the sleep-active ventrolateral preoptic nucleus in the rat,” Neuroscience93(1), 209–214 (1999). [CrossRef] [PubMed]
- C. C. Wu, R. M. Russell, and H. J. Karten, “The transport rate of cholera toxin B subunit in the retinofugal pathways of the chick,” Neuroscience92(2), 665–676 (1999). [CrossRef] [PubMed]
- R. Engelmann and B. A. Sabel, “In vivo imaging of mammalian central nervous system neurons with the in vivo confocal neuroimaging (ICON) method,” Methods Enzymol.307, 563–570 (1999). [CrossRef] [PubMed]
- T. Nakata, S. Terada, and N. Hirokawa, “Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons,” J. Cell Biol.140(3), 659–674 (1998). [CrossRef] [PubMed]
- N. Rivera and N. Lugo, “Four retinal ganglion cell types that project to the superior colliculus in the thirteen-lined ground squirrel (Spermophilus tridecemlineatus),” J. Comp. Neurol.396(1), 105–120 (1998). [CrossRef] [PubMed]
- S. Reuss and K. Decker, “Anterograde tracing of retinohypothalamic afferents with Fluoro-Gold,” Brain Res.745(1-2), 197–204 (1997). [CrossRef] [PubMed]
- B. A. Sabel, R. Engelmann, and M. F. Humphrey, “In vivo confocal neuroimaging (ICON) of CNS neurons,” Nat. Med.3(2), 244–247 (1997). [CrossRef] [PubMed]
- A. Angelucci, F. Clascá, and M. Sur, “Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains,” J. Neurosci. Methods65(1), 101–112 (1996). [CrossRef] [PubMed]
- S. Thanos, J. Kacza, J. Seeger, and J. Mey, “Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo,” Trends Neurosci.17(5), 177–182 (1994). [CrossRef] [PubMed]
- T. A. Viancour and N. A. Kreiter, “Vesicular fast axonal transport rates in young and old rat axons,” Brain Res.628(1-2), 209–217 (1993). [CrossRef] [PubMed]
- J. D. Mikkelsen, “Visualization of efferent retinal projections by immunohistochemical identification of cholera toxin subunit B,” Brain Res. Bull.28(4), 619–623 (1992). [CrossRef] [PubMed]
- M. Hirakawa, J. T. McCabe, and M. Kawata, “Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit,” Cell Tissue Res.267(3), 419–427 (1992). [CrossRef] [PubMed]
- L. Dandona, A. Hendrickson, and H. A. Quigley, “Selective effects of experimental glaucoma on axonal transport by retinal ganglion cells to the dorsal lateral geniculate nucleus,” Invest. Ophthalmol. Vis. Sci.32(5), 1593–1599 (1991). [PubMed]
- P. H. Luppi, P. Fort, and M. Jouvet, “Iontophoretic application of unconjugated cholera toxin B subunit (CTb) combined with immunohistochemistry of neurochemical substances: a method for transmitter identification of retrogradely labeled neurons,” Brain Res.534(1-2), 209–224 (1990). [CrossRef] [PubMed]
- J. J. Quattrochi, A. N. Mamelak, R. D. Madison, J. D. Macklis, and J. A. Hobson, “Mapping neuronal inputs to REM sleep induction sites with carbachol-fluorescent microspheres,” Science245(4921), 984–986 (1989). [CrossRef] [PubMed]
- J. O. Johansson, “Inhibition and recovery of retrograde axoplasmic transport in rat optic nerve during and after elevated IOP in vivo,” Exp. Eye Res.46(2), 223–227 (1988). [CrossRef] [PubMed]
- M. Vidal-Sanz, M. P. Villegas-Pérez, G. M. Bray, and A. J. Aguayo, “Persistent retrograde labeling of adult rat retinal ganglion cells with the carbocyanine dye diI,” Exp. Neurol.102(1), 92–101 (1988). [CrossRef] [PubMed]
- P. H. Luppi, K. Sakai, D. Salvert, P. Fort, and M. Jouvet, “Peptidergic hypothalamic afferents to the cat nucleus raphe pallidus as revealed by a double immunostaining technique using unconjugated cholera toxin as a retrograde tracer,” Brain Res.402(2), 339–345 (1987). [CrossRef] [PubMed]
- A. C. Breuer, M. P. Lynn, M. B. Atkinson, S. M. Chou, A. J. Wilbourn, K. E. Marks, J. E. Culver, and E. J. Fleegler, “Fast axonal transport in amyotrophic lateral sclerosis: an intra-axonal organelle traffic analysis,” Neurology37(5), 738–748 (1987). [CrossRef] [PubMed]
- M. G. Honig and R. I. Hume, “Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures,” J. Cell Biol.103(1), 171–187 (1986). [CrossRef] [PubMed]
- J. O. Johansson, “Retrograde axoplasmic transport in rat optic nerve in vivo. What causes blockage at increased intraocular pressure?” Exp. Eye Res.43(4), 653–660 (1986). [CrossRef] [PubMed]
- L. C. Katz, A. Burkhalter, and W. J. Dreyer, “Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex,” Nature310(5977), 498–500 (1984). [CrossRef] [PubMed]
- R. J. Lasek, J. A. Garner, and S. T. Brady, “Axonal transport of the cytoplasmic matrix,” J. Cell Biol.99(1), 212s–221s (1984). [CrossRef] [PubMed]
- N. K. Gonatas, A. Stieber, J. Gonatas, T. Mommoi, and P. H. Fishman, “Endocytosis of exogenous GM1 ganglioside and cholera toxin by neuroblastoma cells,” Mol. Cell. Biol.3(1), 91–101 (1983). [PubMed]
- C. Davidson, W. R. Green, and V. G. Wong, “Retinal atrophy induced by intravitreous colchicine,” Invest. Ophthalmol. Vis. Sci.24(3), 301–311 (1983). [PubMed]
- X. C. Wan, J. Q. Trojanowski, and J. O. Gonatas, “Cholera toxin and wheat germ agglutinin conjugates as neuroanatomical probes: their uptake and clearance, transganglionic and retrograde transport and sensitivity,” Brain Res.243(2), 215–224 (1982). [CrossRef] [PubMed]
- J. Q. Trojanowski, J. O. Gonatas, and N. K. Gonatas, “Horseradish peroxidase (HRP) conjugates of cholera toxin and lectins are more sensitive retrogradely transported markers than free HRP,” Brain Res.231(1), 33–50 (1982). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Reversibility of optic nerve damage in primate eyes subjected to intraocular pressure above systolic blood pressure,” Br. J. Ophthalmol.65(10), 661–672 (1981). [CrossRef] [PubMed]
- R. L. Radius and D. R. Anderson, “Rapid axonal transport in primate optic nerve. Distribution of pressure-induced interruption,” Arch. Ophthalmol.99(4), 650–654 (1981). [CrossRef] [PubMed]
- I. G. Morgan, “Intraocular colchicine selectively destroys immature ganglion cells in chicken retina,” Neurosci. Lett.24(3), 255–260 (1981). [CrossRef] [PubMed]
- M. M. Black and R. J. Lasek, “Slow components of axonal transport: two cytoskeletal networks,” J. Cell Biol.86(2), 616–623 (1980). [CrossRef] [PubMed]
- H. A. Quigley and E. M. Addicks, “Chronic experimental glaucoma in primates. II. Effect of extended intraocular pressure elevation on optic nerve head and axonal transport,” Invest. Ophthalmol. Vis. Sci.19(2), 137–152 (1980). [PubMed]
- R. L. Radius and D. R. Anderson, “Breakdown of the normal optic nerve head blood-brain barrier following acute elevation of intraocular pressure in experimental animals,” Invest. Ophthalmol. Vis. Sci.19(3), 244–255 (1980). [PubMed]
- R. L. Radius, E. L. Schwartz, and D. R. Anderson, “Failure of unilateral carotid artery ligation to affect pressure-induced interruption of rapid axonal transport in primate optic nerves,” Invest. Ophthalmol. Vis. Sci.19(2), 153–157 (1980). [PubMed]
- B. Grafstein and D. S. Forman, “Intracellular transport in neurons,” Physiol. Rev.60(4), 1167–1283 (1980). [PubMed]
- H. A. Quigley, J. Guy, and D. R. Anderson, “Blockade of rapid axonal transport. Effect of intraocular pressure elevation in primate optic nerve,” Arch. Ophthalmol.97(3), 525–531 (1979). [CrossRef] [PubMed]
- P. W. Land and R. D. Lund, “Development of the rat’s uncrossed retinotectal pathway and its relation to plasticity studies,” Science205(4407), 698–700 (1979). [CrossRef] [PubMed]
- K. C. Joseph, S. U. Kim, A. Stieber, and N. K. Gonatas, “Endocytosis of cholera toxin into neuronal GERL,” Proc. Natl. Acad. Sci. U.S.A.75(6), 2815–2819 (1978). [CrossRef] [PubMed]
- D. S. Minckler, A. H. Bunt, and I. B. Klock, “Radioautographic and cytochemical ultrastructural studies of axoplasmic transport in the monkey optic nerve head,” Invest. Ophthalmol. Vis. Sci.17(1), 33–50 (1978). [PubMed]
- D. Gaasterland, T. Tanishima, and T. Kuwabara, “Axoplasmic flow during chronic experimental glaucoma. 1. Light and electron microscopic studies of the monkey optic nervehead during development of glaucomatous cupping,” Invest. Ophthalmol. Vis. Sci.17(9), 838–846 (1978). [PubMed]
- D. S. Minckler, A. H. Bunt, and G. W. Johanson, “Orthograde and retrograde axoplasmic transport during acute ocular hypertension in the monkey,” Invest. Ophthalmol. Vis. Sci.16(5), 426–441 (1977). [PubMed]
- H. A. Quigley and D. R. Anderson, “Distribution of axonal transport blockade by acute intraocular pressure elevation in the primate optic nerve head,” Invest. Ophthalmol. Vis. Sci.16(7), 640–644 (1977). [PubMed]
- M. E. Schwab and H. Thoenen, “Retrograde axonal and transsynaptic transport of macromolecules: physiological and pathophysiological importance,” Agents Actions7(3), 361–368 (1977). [CrossRef] [PubMed]
- H. Quigley and D. R. Anderson, “The dynamics and location of axonal transport blockade by acute intraocular pressure elevation in primate optic nerve,” Invest. Ophthalmol.15(8), 606–616 (1976). [PubMed]
- R. D. Lund and S. D. Hauschka, “Transplanted neural tissue develops connections with host rat brain,” Science193(4253), 582–584 (1976). [CrossRef] [PubMed]
- U. C. Dräger and D. H. Hubel, “Topography of visual and somatosensory projections to mouse superior colliculus,” J. Neurophysiol.39(1), 91–101 (1976). [PubMed]
- D. R. Anderson and A. Hendrickson, “Effect of intraocular pressure on rapid axoplasmic transport in monkey optic nerve,” Invest. Ophthalmol.13(10), 771–783 (1974). [PubMed]
- S. Ochs, “Fast transport of materials in mammalian nerve fibers,” Science176(4032), 252–260 (1972). [CrossRef] [PubMed]
- J. O. Karlsson, H. A. Hansson, and J. Sjöstrand, “Effect of colchicine on axonal transport and morphology of retinal ganglion cells,” Z. Zellforsch. Mikrosk. Anat.115(2), 265–283 (1971). [CrossRef] [PubMed]
- K. A. James, J. J. Bray, I. G. Morgan, and L. Austin, “The effect of colchicine on the transport of axonal protein in the chicken,” Biochem. J.117(4), 767–771 (1970). [PubMed]
- G. W. Kreutzberg, “Neuronal dynamics and axonal flow. IV. Blockage of intra-axonal enzyme transport by colchicine,” Proc. Natl. Acad. Sci. U.S.A.62(3), 722–728 (1969). [CrossRef] [PubMed]
- J. O. Karlsson and J. Sjöstrand, “The effect of colchicine on the axonal transport of protein in the optic nerve and tract of the rabbit,” Brain Res.13(3), 617–619 (1969). [CrossRef] [PubMed]
- A. Dahlström, “Effect of colchicine on transport of amine storage granules in sympathetic nerves of rat,” Eur. J. Pharmacol.5(1), 111–113 (1968). [CrossRef] [PubMed]
- P. W. Lampert, M. H. Vogel, and L. E. Zimmerman, “Pathology of the optic nerve in experimental acute glaucoma. Electron microscopic studies,” Invest. Ophthalmol.7(2), 199–213 (1968). [PubMed]
- S. Inoue, “The effect of colchicine on the microscopic and submicroscopic structure of the mitotic spindle,” Exp. Cell Res. Suppl.2, 305–318 (1952).
- O. J. Eigsti, “A cytological study of colchicine effects in the induction of polyploidy in plants,” Proc. Natl. Acad. Sci. U.S.A.24(2), 56–63 (1938). [CrossRef] [PubMed]
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