Optics InfoBase > Virtual Journal for Biomedical Optics > Volume 4 > Issue 10 > Page 14418
Estimation of the effective orientation of the SHG source in primary cortical neurons
Sotiris Psilodimitrakopoulos, Valerie Petegnief, Guadalupe Soria, Ivan Amat-Roldan, David Artigas, Anna M. Planas, and Pablo Loza-Alvarez »View Author Affiliations
1ICFO-Institut de Ciéncies Fotòniques, Mediterranean Technology Park, 08860 Castelldefels (Barcelona), Spain
2Department of Brain Ischemia and Neurodegeneration, Institute for Biomedical Research of Barcelona (IIBB), Spanish Research Council (CSIC), Institut d’Investigacions Biomédiques August Pi Sunyer (IDIBAPS), Barcelona, Spain
3UPC- Universitat Politécnica de Catalunya, Department of signal theory and communications, 08034, Barcelona, Spain
*pablo.loza@icfo.es
Optics Express, Vol. 17, Issue 16, pp. 14418-14425 (2009)
http://dx.doi.org/10.1364/OE.17.014418
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Abstract
In this paper we provide, for the first time to our knowledge, the effective orientation of the SHG source in cultured cortical neuronal processes in vitro. This is done by the use of the polarization sensitive second harmonic generation (PSHG) imaging microscopy technique. By performing a pixel-level resolution analysis we found that the SHG dipole source has a distribution of angles centered at θe =33.96°, with a bandwidth of Δθe = 12.85°. This orientation can be related with the molecular geometry of the tubulin heterodimmer contained in microtubules.
© 2009 OSA
OCIS Codes
(170.3880) Medical optics and biotechnology : Medical and biological imaging
(180.5810) Microscopy : Scanning microscopy
(190.1900) Nonlinear optics : Diagnostic applications of nonlinear optics
(190.2620) Nonlinear optics : Harmonic generation and mixing
(180.4315) Microscopy : Nonlinear microscopy
(110.5405) Imaging systems : Polarimetric imaging
(170.6935) Medical optics and biotechnology : Tissue characterization
ToC Category:
Medical Optics and Biotechnology
History
Original Manuscript: June 18, 2009
Revised Manuscript: July 22, 2009
Manuscript Accepted: July 27, 2009
Published: July 31, 2009
Virtual Issues
Vol. 4, Iss. 10 Virtual Journal for Biomedical Optics
Citation
Sotiris Psilodimitrakopoulos, Valerie Petegnief, Guadalupe Soria, Ivan Amat-Roldan, David Artigas, Anna M. Planas, and Pablo Loza-Alvarez, "Estimation of the effective orientation of the SHG source in primary cortical neurons," Opt. Express 17, 14418-14425 (2009)
http://www.opticsinfobase.org/vjbo/abstract.cfm?URI=oe-17-16-14418
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References
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- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
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- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
- O. Nadiarnykh and P. J. Campagnola, “Retention of polarization signatures in SHG microscopy of scattering tissues through optical clearing,” Opt. Express 17(7), 5794–5806 (2009). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
- I. Freund, M. Deutsch, and A. Sprecher, “Connective tissue polarity. Optical second-harmonic microscopy, crossed-beam summation, and small-angle scattering in rat-tail tendon,” Biophys. J. 50(4), 693–712 (1986). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- K. J. De Vos, A. J. Grierson, S. Ackerley, and C. C. J. Miller, “Role of axonal transport in neurodegenerative diseases,” Annu. Rev. Neurosci. 31(1), 151–173 (2008). [CrossRef] [PubMed]
- A. Akhmanova and M. O. Steinmetz, “Tracking the ends: a dynamic protein network controls the fate of microtubule tips,” Nat. Rev. Mol. Cell Biol. 9(4), 309–322 (2008). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, D. Artigas, G. Soria, I. Amat-Roldan, A. M. Planas, and P. Loza-Alvarez, “Quantitative discrimination between endogenous SHG sources in mammalian tissue, based on their polarization response,” Opt. Express 17(12), 10168–10176 (2009). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, D. Artigas, G. Soria, I. Amat-Roldan, A. M. Planas, and P. Loza-Alvarez, “Quantitative discrimination between endogenous SHG sources in mammalian tissue, based on their polarization response,” Opt. Express 17(12), 10168–10176 (2009). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- W. H. Stoothoff, B. J. Bacskai, and B. T. Hyman, “Monitoring tau-tubulin interactions utilizing second harmonic generation in living neurons,” J. Biomed. Opt. 13(6), 064039 (2008). [CrossRef]
- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- O. Nadiarnykh and P. J. Campagnola, “Retention of polarization signatures in SHG microscopy of scattering tissues through optical clearing,” Opt. Express 17(7), 5794–5806 (2009). [CrossRef] [PubMed]
- S. V. Plotnikov, A. C. Millard, P. J. Campagnola, and W. A. Mohler, “Characterization of the myosin-based source for second harmonic generation from muscle sarcomeres,” Biophys. J. 90, 693–703 (2006). [CrossRef]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- P. J. Campagnola, M. D. Wei, A. Lewis, and L. M. Loew, “High-resolution nonlinear optical imaging of live cells by second harmonic generation,” Biophys. J. 77(6), 3341–3349 (1999). [CrossRef] [PubMed]
- S. Saxena and P. Caroni, “Mechanisms of axon degeneration: from development to disease,” Prog. Neurobiol. 83(3), 174–191 (2007). [CrossRef] [PubMed]
- P. Stoller, K. M. Reiser, P. M. Celliers, and A. M. Rubenchik, “Polarization-modulated second harmonic generation in collagen,” Biophys. J. 82(6), 3330–3342 (2002). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
- K. J. De Vos, A. J. Grierson, S. Ackerley, and C. C. J. Miller, “Role of axonal transport in neurodegenerative diseases,” Annu. Rev. Neurosci. 31(1), 151–173 (2008). [CrossRef] [PubMed]
- I. Freund, M. Deutsch, and A. Sprecher, “Connective tissue polarity. Optical second-harmonic microscopy, crossed-beam summation, and small-angle scattering in rat-tail tendon,” Biophys. J. 50(4), 693–712 (1986). [CrossRef] [PubMed]
- A. C. Kwan, D. A. Dombeck, and W. W. Webb, “Polarized microtubule arrays in apical dendrites and axons,” Proc. Natl. Acad. Sci. U.S.A. 105(32), 11370–11375 (2008). [CrossRef] [PubMed]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
- H. P. Erickson, “Microtubule surface lattice and subunit structure and observations on reassembly,” J. Cell Biol. 60(1), 153–167 (1974). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
- I. Freund, M. Deutsch, and A. Sprecher, “Connective tissue polarity. Optical second-harmonic microscopy, crossed-beam summation, and small-angle scattering in rat-tail tendon,” Biophys. J. 50(4), 693–712 (1986). [CrossRef] [PubMed]
- S. Roth and I. Freund, “Second harmonic generation in collagen,” J. Chem. Phys. 70(4), 1637–1643 (1979). [CrossRef]
- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
- K. J. De Vos, A. J. Grierson, S. Ackerley, and C. C. J. Miller, “Role of axonal transport in neurodegenerative diseases,” Annu. Rev. Neurosci. 31(1), 151–173 (2008). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- W. H. Stoothoff, B. J. Bacskai, and B. T. Hyman, “Monitoring tau-tubulin interactions utilizing second harmonic generation in living neurons,” J. Biomed. Opt. 13(6), 064039 (2008). [CrossRef]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
- A. C. Kwan, K. Duff, G. K. Gouras, and W. W. Webb, “Optical visualization of Alzheimer’s pathology via multiphoton-excited intrinsic fluorescence and second harmonic generation,” Opt. Express 17(5), 3679–3689 (2009). [CrossRef] [PubMed]
- A. C. Kwan, D. A. Dombeck, and W. W. Webb, “Polarized microtubule arrays in apical dendrites and axons,” Proc. Natl. Acad. Sci. U.S.A. 105(32), 11370–11375 (2008). [CrossRef] [PubMed]
- C. Odin, C. Heichette, D. Chretien, and Y. Le Grand, “Second harmonic microscopy of axonemes,” Opt. Express 17(11), 9235–9240 (2009). [CrossRef] [PubMed]
- C. Odin, T. Guilbert, A. Alkilani, O. P. Boryskina, V. Fleury, and Y. Le Grand, “Collagen and myosin characterization by orientation field second harmonic microscopy,” Opt. Express 16(20), 16151–16165 (2008). [CrossRef] [PubMed]
- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- P. J. Campagnola, M. D. Wei, A. Lewis, and L. M. Loew, “High-resolution nonlinear optical imaging of live cells by second harmonic generation,” Biophys. J. 77(6), 3341–3349 (1999). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
- P. J. Campagnola, M. D. Wei, A. Lewis, and L. M. Loew, “High-resolution nonlinear optical imaging of live cells by second harmonic generation,” Biophys. J. 77(6), 3341–3349 (1999). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, D. Artigas, G. Soria, I. Amat-Roldan, A. M. Planas, and P. Loza-Alvarez, “Quantitative discrimination between endogenous SHG sources in mammalian tissue, based on their polarization response,” Opt. Express 17(12), 10168–10176 (2009). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- S. V. Plotnikov, A. C. Millard, P. J. Campagnola, and W. A. Mohler, “Characterization of the myosin-based source for second harmonic generation from muscle sarcomeres,” Biophys. J. 90, 693–703 (2006). [CrossRef]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- K. J. De Vos, A. J. Grierson, S. Ackerley, and C. C. J. Miller, “Role of axonal transport in neurodegenerative diseases,” Annu. Rev. Neurosci. 31(1), 151–173 (2008). [CrossRef] [PubMed]
- S. V. Plotnikov, A. C. Millard, P. J. Campagnola, and W. A. Mohler, “Characterization of the myosin-based source for second harmonic generation from muscle sarcomeres,” Biophys. J. 90, 693–703 (2006). [CrossRef]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- C. Odin, C. Heichette, D. Chretien, and Y. Le Grand, “Second harmonic microscopy of axonemes,” Opt. Express 17(11), 9235–9240 (2009). [CrossRef] [PubMed]
- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
- C. Odin, T. Guilbert, A. Alkilani, O. P. Boryskina, V. Fleury, and Y. Le Grand, “Collagen and myosin characterization by orientation field second harmonic microscopy,” Opt. Express 16(20), 16151–16165 (2008). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, D. Artigas, G. Soria, I. Amat-Roldan, A. M. Planas, and P. Loza-Alvarez, “Quantitative discrimination between endogenous SHG sources in mammalian tissue, based on their polarization response,” Opt. Express 17(12), 10168–10176 (2009). [CrossRef] [PubMed]
- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
- S. V. Plotnikov, A. C. Millard, P. J. Campagnola, and W. A. Mohler, “Characterization of the myosin-based source for second harmonic generation from muscle sarcomeres,” Biophys. J. 90, 693–703 (2006). [CrossRef]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, D. Artigas, G. Soria, I. Amat-Roldan, A. M. Planas, and P. Loza-Alvarez, “Quantitative discrimination between endogenous SHG sources in mammalian tissue, based on their polarization response,” Opt. Express 17(12), 10168–10176 (2009). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
- P. Stoller, K. M. Reiser, P. M. Celliers, and A. M. Rubenchik, “Polarization-modulated second harmonic generation in collagen,” Biophys. J. 82(6), 3330–3342 (2002). [CrossRef] [PubMed]
- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- S. Roth and I. Freund, “Second harmonic generation in collagen,” J. Chem. Phys. 70(4), 1637–1643 (1979). [CrossRef]
- F. Tiaho, G. Recher, and D. Rouède, “Estimation of helical angles of myosin and collagen by second harmonic generation imaging microscopy,” Opt. Express 15(19), 12286–12295 (2007). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- P. Stoller, K. M. Reiser, P. M. Celliers, and A. M. Rubenchik, “Polarization-modulated second harmonic generation in collagen,” Biophys. J. 82(6), 3330–3342 (2002). [CrossRef] [PubMed]
- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- S. Saxena and P. Caroni, “Mechanisms of axon degeneration: from development to disease,” Prog. Neurobiol. 83(3), 174–191 (2007). [CrossRef] [PubMed]
- I. Freund, M. Deutsch, and A. Sprecher, “Connective tissue polarity. Optical second-harmonic microscopy, crossed-beam summation, and small-angle scattering in rat-tail tendon,” Biophys. J. 50(4), 693–712 (1986). [CrossRef] [PubMed]
- A. Akhmanova and M. O. Steinmetz, “Tracking the ends: a dynamic protein network controls the fate of microtubule tips,” Nat. Rev. Mol. Cell Biol. 9(4), 309–322 (2008). [CrossRef] [PubMed]
- P. Stoller, K. M. Reiser, P. M. Celliers, and A. M. Rubenchik, “Polarization-modulated second harmonic generation in collagen,” Biophys. J. 82(6), 3330–3342 (2002). [CrossRef] [PubMed]
- W. H. Stoothoff, B. J. Bacskai, and B. T. Hyman, “Monitoring tau-tubulin interactions utilizing second harmonic generation in living neurons,” J. Biomed. Opt. 13(6), 064039 (2008). [CrossRef]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
- A. C. Kwan, K. Duff, G. K. Gouras, and W. W. Webb, “Optical visualization of Alzheimer’s pathology via multiphoton-excited intrinsic fluorescence and second harmonic generation,” Opt. Express 17(5), 3679–3689 (2009). [CrossRef] [PubMed]
- A. C. Kwan, D. A. Dombeck, and W. W. Webb, “Polarized microtubule arrays in apical dendrites and axons,” Proc. Natl. Acad. Sci. U.S.A. 105(32), 11370–11375 (2008). [CrossRef] [PubMed]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
- P. J. Campagnola, M. D. Wei, A. Lewis, and L. M. Loew, “High-resolution nonlinear optical imaging of live cells by second harmonic generation,” Biophys. J. 77(6), 3341–3349 (1999). [CrossRef] [PubMed]
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
Annu. Rev. Neurosci.
- K. J. De Vos, A. J. Grierson, S. Ackerley, and C. C. J. Miller, “Role of axonal transport in neurodegenerative diseases,” Annu. Rev. Neurosci. 31(1), 151–173 (2008). [CrossRef] [PubMed]
Biochem. J.
- V. Petegnief, M. Font-Nieves, M. E. Martín, M. Salinas, and A. M. Planas, “Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis,” Biochem. J. 411(3), 667–677 (2008). [CrossRef] [PubMed]
Biophys. J.
- I. Freund, M. Deutsch, and A. Sprecher, “Connective tissue polarity. Optical second-harmonic microscopy, crossed-beam summation, and small-angle scattering in rat-tail tendon,” Biophys. J. 50(4), 693–712 (1986). [CrossRef] [PubMed]
- P. Stoller, K. M. Reiser, P. M. Celliers, and A. M. Rubenchik, “Polarization-modulated second harmonic generation in collagen,” Biophys. J. 82(6), 3330–3342 (2002). [CrossRef] [PubMed]
- S. W. Chu, S. Y. Chen, G. W. Chern, T. H. Tsai, Y. C. Chen, B. L. Lin, and C. K. Sun, “Studies of χ(2)/χ(3) tensors in submicron-scaled bio-tissues by polarization harmonics optical microscopy,” Biophys. J. 86(6), 3914–3922 (2004). [CrossRef] [PubMed]
- S. V. Plotnikov, A. C. Millard, P. J. Campagnola, and W. A. Mohler, “Characterization of the myosin-based source for second harmonic generation from muscle sarcomeres,” Biophys. J. 90, 693–703 (2006). [CrossRef]
- P. J. Campagnola, A. C. Millard, M. Terasaki, P. E. Hoppe, C. J. Malone, and W. A. Mohler, “Three – dimensional high-resolution second harmonic generation imaging of endogenous structural proteins in biological tissues,” Biophys. J. 82(1), 493–508 (2002). [CrossRef]
- P. J. Campagnola, M. D. Wei, A. Lewis, and L. M. Loew, “High-resolution nonlinear optical imaging of live cells by second harmonic generation,” Biophys. J. 77(6), 3341–3349 (1999). [CrossRef] [PubMed]
J. Biomed. Opt.
- W. H. Stoothoff, B. J. Bacskai, and B. T. Hyman, “Monitoring tau-tubulin interactions utilizing second harmonic generation in living neurons,” J. Biomed. Opt. 13(6), 064039 (2008). [CrossRef]
- G. Filippidis, C. Kouloumentas, G. Voglis, F. Zacharopoulou, T. G. Papazoglou, and N. Tavernarakis, “Imaging of Caenorhabditis elegans neurons by second-harmonic generation and two-photon excitation fluorescence,” J. Biomed. Opt. 10(2), 024015–024018 (2005). [CrossRef] [PubMed]
- S. Y. Chen, C. S. Hsieh, S. W. Chu, C. Y. Lin, C. Y. Ko, Y. C. Chen, H. J. Tsai, C. H. Hu, and C. K. Sun, “Noninvasive harmonics optical microscopy for long-term observation of embryonic nervous system development in vivo,” J. Biomed. Opt. 11(5), 054022–054028 (2006). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, S. Santos, I. Amat-Roldan, A. K. Thayil, D. Artigas, and P. Loza-Alvarez, “In vivo, pixel-resolution mapping of thick filaments’ orientation in nonfibrilar muscle using polarization-sensitive second harmonic generation microscopy,” J. Biomed. Opt. 14(1), 014001–014011 (2009). [CrossRef] [PubMed]
- A. Erikson, J. Örtegren, T. Hompland, C. de Lange Davies, and M. Lindgren, “Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope,” J. Biomed. Opt. 12(4), 044002–044010 (2007). [CrossRef] [PubMed]
J. Cell Biol.
- H. P. Erickson, “Microtubule surface lattice and subunit structure and observations on reassembly,” J. Cell Biol. 60(1), 153–167 (1974). [CrossRef] [PubMed]
J. Chem. Phys.
- S. Roth and I. Freund, “Second harmonic generation in collagen,” J. Chem. Phys. 70(4), 1637–1643 (1979). [CrossRef]
J. Microsc.
- C. Odin, Y. Le Grand, A. Renault, L. Gailhouste, and G. Baffet, “Orientation fields of nonlinear biological fibrils by second harmonic generation microscopy,” J. Microsc. 229(Pt 1), 32–38 (2008). [CrossRef] [PubMed]
- K. N. Anisha Thayil, E. J. Gualda, S. Psilodimitrakopoulos, I. G. Cormack, I. Amat-Roldán, M. Mathew, D. Artigas, and P. Loza-Alvarez, “Starch-based backwards SHG for in situ MEFISTO pulse characterization in multiphoton microscopy,” J. Microsc. 230(Pt 1), 70–75 (2008). [CrossRef] [PubMed]
Langmuir
- A. Leray, L. Leroy, Y. Le Grand, C. Odin, A. Renault, V. Vié, D. Rouède, T. Mallegol, O. Mongin, M. H. V. Werts, and M. Blanchard-Desce, “Organization and orientation of amphiphilic push-pull chromophores deposited in Langmuir-Blodgett monolayers studied by second harmonic generation and atomic force microscopy,” Langmuir 20(19), 8165–8171 (2004). [CrossRef] [PubMed]
Nat. Rev. Mol. Cell Biol.
- A. Akhmanova and M. O. Steinmetz, “Tracking the ends: a dynamic protein network controls the fate of microtubule tips,” Nat. Rev. Mol. Cell Biol. 9(4), 309–322 (2008). [CrossRef] [PubMed]
Opt. Express
- A. C. Kwan, K. Duff, G. K. Gouras, and W. W. Webb, “Optical visualization of Alzheimer’s pathology via multiphoton-excited intrinsic fluorescence and second harmonic generation,” Opt. Express 17(5), 3679–3689 (2009). [CrossRef] [PubMed]
- O. Nadiarnykh and P. J. Campagnola, “Retention of polarization signatures in SHG microscopy of scattering tissues through optical clearing,” Opt. Express 17(7), 5794–5806 (2009). [CrossRef] [PubMed]
- C. Odin, T. Guilbert, A. Alkilani, O. P. Boryskina, V. Fleury, and Y. Le Grand, “Collagen and myosin characterization by orientation field second harmonic microscopy,” Opt. Express 16(20), 16151–16165 (2008). [CrossRef] [PubMed]
- S. Psilodimitrakopoulos, D. Artigas, G. Soria, I. Amat-Roldan, A. M. Planas, and P. Loza-Alvarez, “Quantitative discrimination between endogenous SHG sources in mammalian tissue, based on their polarization response,” Opt. Express 17(12), 10168–10176 (2009). [CrossRef] [PubMed]
- F. Tiaho, G. Recher, and D. Rouède, “Estimation of helical angles of myosin and collagen by second harmonic generation imaging microscopy,” Opt. Express 15(19), 12286–12295 (2007). [CrossRef] [PubMed]
- C. Odin, C. Heichette, D. Chretien, and Y. Le Grand, “Second harmonic microscopy of axonemes,” Opt. Express 17(11), 9235–9240 (2009). [CrossRef] [PubMed]
Proc. Natl. Acad. Sci. U.S.A.
- A. C. Kwan, D. A. Dombeck, and W. W. Webb, “Polarized microtubule arrays in apical dendrites and axons,” Proc. Natl. Acad. Sci. U.S.A. 105(32), 11370–11375 (2008). [CrossRef] [PubMed]
- D. A. Dombeck, K. A. Kasischke, H. D. Vishwasrao, M. Ingelsson, B. T. Hyman, and W. W. Webb, “Uniform polarity microtubule assemblies imaged in native brain tissue by second-harmonic generation microscopy,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7081–7086 (2003). [CrossRef] [PubMed]
Prog. Neurobiol.
- S. Saxena and P. Caroni, “Mechanisms of axon degeneration: from development to disease,” Prog. Neurobiol. 83(3), 174–191 (2007). [CrossRef] [PubMed]
2009, Psilodimitrakopoulos, J. Biomed. Opt.
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