OSA's Digital Library

Biomedical Optics Express

Biomedical Optics Express

  • Editor: Joseph A. Izatt
  • Vol. 2, Iss. 1 — Jan. 1, 2011
  • pp: 139–148
« Show journal navigation

Images of photoreceptors in living primate eyes using adaptive optics two-photon ophthalmoscopy

Jennifer J. Hunter, Benjamin Masella, Alfredo Dubra, Robin Sharma, Lu Yin, William H. Merigan, Grazyna Palczewska, Krzysztof Palczewski, and David R. Williams  »View Author Affiliations


Biomedical Optics Express, Vol. 2, Issue 1, pp. 139-148 (2011)
http://dx.doi.org/10.1364/BOE.2.000139


View Full Text Article

Acrobat PDF (1193 KB)





Browse Journals / Lookup Meetings

Browse by Journal and Year


   


Lookup Conference Papers

Close Browse Journals / Lookup Meetings

Article Tools

Share
Citations

Abstract

In vivo two-photon imaging through the pupil of the primate eye has the potential to become a useful tool for functional imaging of the retina. Two-photon excited fluorescence images of the macaque cone mosaic were obtained using a fluorescence adaptive optics scanning laser ophthalmoscope, overcoming the challenges of a low numerical aperture, imperfect optics of the eye, high required light levels, and eye motion. Although the specific fluorophores are as yet unknown, strong in vivo intrinsic fluorescence allowed images of the cone mosaic. Imaging intact ex vivo retina revealed that the strongest two-photon excited fluorescence signal comes from the cone inner segments. The fluorescence response increased following light stimulation, which could provide a functional measure of the effects of light on photoreceptors.

© 2010 OSA

1. Introduction

Human vision following light absorption by the retina is dependent on an initial phototransduction cascade that generates photocurrent and the subsequent regeneration of photopigments [1

1. T. D. Lamb and E. N. Pugh Jr., “Dark adaptation and the retinoid cycle of vision,” Prog. Retin. Eye Res. 23(3), 307–380 (2004). [CrossRef] [PubMed]

]. Much of our understanding of both these processes comes from in vitro work and animal models. Investigation of these pathways has been severely limited by difficulties in observing them in living eyes. However, it is valuable to study these processes in vivo in part because defects in these pathways can lead to irreversible blindness [2

2. G. H. Travis, M. Golczak, A. R. Moise, and K. Palczewski, “Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents,” Annu. Rev. Pharmacol. Toxicol. 47(1), 469–512 (2007). [CrossRef] [PubMed]

]. Though the kinetics of rod and cone photopigments have been extensively investigated for more than 50 years, functional measurements of other relevant molecules have not been possible. Here, we describe a new imaging method that marries adaptive optics and two-photon fluorescence imaging to demonstrate light dependent changes in individual photoreceptors inside the living primate eye. This technique could allow noninvasive monitoring of photoreceptor function in normal and diseased eyes.

The poor optical quality of the mammalian eye and its rapid involuntary ocular motion generally precludes imaging at cellular resolution, but recent advances in high-resolution imaging with a fluorescence adaptive optics scanning laser ophthalmoscope (FAOSLO) coupled with novel image registration methods can overcome this difficulty [3

3. 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. Express 14(16), 7144–7158 (2006). [CrossRef] [PubMed]

5

5. J. I. Morgan, A. Dubra, R. Wolfe, W. H. Merigan, and D. R. Williams, “In vivo autofluorescence imaging of the human and macaque retinal pigment epithelial cell mosaic,” Invest. Ophthalmol. Vis. Sci. 50(3), 1350–1359 (2008). [CrossRef] [PubMed]

]. Adaptive optics allows high-resolution imaging with the largest numerical aperture that can be obtained with a dilated pupil. Fluorescence imaging produces high contrast images of otherwise invisible structures. Although there are many different intrinsically-fluorescent molecules in the retina, many cannot be accessed in the living eye by single-photon fluorescence imaging. Excitation spectra for several molecules involved in photoreceptor function [6

6. C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]

] fall below 400 nm, where the eye’s optics prevent light from reaching the retina [7

7. J. Dillon, L. Zheng, J. C. Merriam, and E. R. Gaillard, “Transmission spectra of light to the mammalian retina,” Photochem. Photobiol. 71(2), 225–229 (2000). [CrossRef] [PubMed]

]. We capitalized on two-photon excited fluorescence by using a near infrared excitation wavelength to excite otherwise inaccessible fluorophores and produce the intrinsic contrast for imaging retinal structure. Two-photon fluorescence provides intrinsic axial resolution by preferentially exciting fluorophores near the focal plane. In addition, two-photon imaging will permit separation of functional imaging of retinal neurons from the intense visual stimulation that is produced by current single-photon imaging [3

3. 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. Express 14(16), 7144–7158 (2006). [CrossRef] [PubMed]

,4

4. J. I. Morgan, J. J. Hunter, B. Masella, R. Wolfe, D. C. Gray, W. H. Merigan, F. C. Delori, and D. R. Williams, “Light-induced retinal changes observed with high-resolution autofluorescence imaging of the retinal pigment epithelium,” Invest. Ophthalmol. Vis. Sci. 49(8), 3715–3729 (2008). [CrossRef] [PubMed]

].

2. Methods

2.1. Fluorescence adaptive optics scanning laser ophthalmoscope (FAOSLO)

High-resolution images of the retina were obtained with a fluorescence adaptive optics scanning laser ophthalmoscope (FAOSLO). This second generation instrument (Fig. 1
Fig. 1 Schematic of the FAOSLO system. Changes in the vertical plane are outlined by the dashed lines. Inset: A plot of the transmission spectrum for two-photon emission collection into the detector. DM, deformable mirror; HS, horizontal scanner; LD, laser diode; PMT, photomultiplier tube; SLD, superluminescent diode; VS, vertical scanner; WFS, wavefront sensor.
) is similar to the first generation FAOSLO previously described in detail [3

3. 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. Express 14(16), 7144–7158 (2006). [CrossRef] [PubMed]

]. For reflectance imaging, a 790 nm (ΔFWHM 17 nm) superluminescent diode (Broadlighter, Superlum Ireland, Carrigtwohill, Co. Cork, Ireland) was used. The source for wavefront sensing was a 904 nm laser diode. For two-photon excitation at 730 nm, the source was a Ti-sapphire laser (Mai Tai, Newport Spectra-Physics, Santa Clara, CA, USA) equipped with second-order dispersion compensation (DeepSee, Newport Spectra-Physics, Santa Clara, CA, USA). This source had an 80 MHz repetition rate and a pulse width less than 70 fs in air. During calibration, a water chamber equal in length to the axial length of a macaque eye with a sample of fluorescein beads was used to determine the optimum setting (peak at 21.64 ± 0.13 standard error of the mean) for dispersion compensation. Light reflected from the retina retraced the system’s optical path and was collected through a confocal pinhole by a photomultiplier tube (H7422-50, Hamamatsu, Japan). To maximize efficiency for two-photon imaging, emitted fluorescence from the eye was collected without being descanned. This required that the eye’s pupil be imaged onto a second photomultiplier tube (H7422-40, Hamamatsu, Japan) after being reflected off a dichroic (FF665-Di02, Semrock, Rochester, NY, USA). The emitted fluorescene passed through two identical emission filters (E550sp-2p, Chroma, Bellows Falls, VT, USA) to prevent bleed-through from the imaging sources. Both reflectance and fluorescence images were reconstructed based on the known positions of the scanners at a given point in time. All images were acquired at 25Hz with 256 gray levels (8-bit depth).

Adaptive optics was employed to overcome the poor optical quality of the primate eye and create a near diffraction-limited spot on the retina. A Hartmann-Shack wavefront sensor (lenslet array with a pitch of 203 μm and a focal length of 7.8 mm, having 30 lenslets across a 7.2 mm diameter pupil as imaged into the eye’s pupil) was used to measure optical aberrations of the eye, which then were corrected with a deformable mirror (Hi-Speed dm97, ALPAO, Biviers, France). Magnification from the eye to the lenslet array was 0.87. The adaptive optics correction was operated at 10 Hz and ran in closed-loop during image acquisition.

To compensate for the low fluorescence emission in a standard two-photon microscope, light at each pixel is integrated for a long period of time, but this is not possible in the living eye because of continual motion. Instead, up to 16,500 individual fluorescence frames (12 minute acquisition) were registered and added together to produce the final image. Dual-image capture and registration (custom software, DeMotion [8

8. A. Dubra and Z. Harvey, “Registration of 2D images from fast scanning ophthalmic instruments” presented at WBIR 2010—Workshop on Biomedical Image Registration, July 11–13 2010, Lübeck, Germany.

]), in which the motion trace of a simultaneously obtained high signal-to-noise ratio (SNR) reflectance image is used to register a low SNR fluorescence video, was needed [3

3. 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. Express 14(16), 7144–7158 (2006). [CrossRef] [PubMed]

5

5. J. I. Morgan, A. Dubra, R. Wolfe, W. H. Merigan, and D. R. Williams, “In vivo autofluorescence imaging of the human and macaque retinal pigment epithelial cell mosaic,” Invest. Ophthalmol. Vis. Sci. 50(3), 1350–1359 (2008). [CrossRef] [PubMed]

]. In addition, to compensate for the longitudinal chromatic aberration of the eye, the reflectance and two-photon excited fluorescence inputs were pre-adjusted to be focused on the same plane within the eye.

2.2. FAOSLO imaging procedure

In vivo macaque (macaca mulatta) retinas were imaged during sessions lasting up to 6 hours. Primates were prepared for imaging according to procedures previously described in detail [4

4. J. I. Morgan, J. J. Hunter, B. Masella, R. Wolfe, D. C. Gray, W. H. Merigan, F. C. Delori, and D. R. Williams, “Light-induced retinal changes observed with high-resolution autofluorescence imaging of the retinal pigment epithelium,” Invest. Ophthalmol. Vis. Sci. 49(8), 3715–3729 (2008). [CrossRef] [PubMed]

]. Primates were anaesthetized with an intramuscular injection of ketamine, diazepam and glycopyrrolate, then intubated and kept in deep stage III, plane 3 anaesthesia with isofluorane. Mydriasis and cycloplegia were induced with 1-2 drops each of 2.5% phenylephrine hydrochloride and 1% tropicamide. During imaging the eye was held open with a lid speculum and a rigid gas permeable contact lens was placed over the cornea to maintain corneal health and optical quality. The macaque’s head post was attached to a gimbal mount designed to rotate about the eye’s pupil and a translation stage provided minor pupil adjustments. Multiple locations across the macula could be imaged by adjusting the gimbal mount. Two-photon imaging was performed repeatedly at a given location under variable conditions. Variables included the plane of focus, incident excitation power and dispersion compensation. Image acquisition at 6 locations began just prior to onset of the excitation laser, allowing fluorescence changes in response to the bleaching excitation light to be measured.

In addition to FAOSLO imaging, fundus photography and fluorescein angiography were performed before and after initial FAOSLO imaging sessions to monitor retinal health and check for signs of light damage. The axial length of each eye was determined as the average of 10 A-scan ultrasound measurements (Quality Diagnostic Ultrasound, Storz/Teknar) and was used to convert the angular scale of the image to a linear scale on the retina according to the LeGrand eye model [9

9. G. Wyszecki, and W. S. Stiles, Color Science: Concepts and Methods, Quantitative Data and Formulae (John Wiley & Sons, Inc., 1982).

]. Retinal eccentricity was based on the distance from the foveal center for each imaged location when overlaid on a fundus photo. All animal procedures were approved by the University Committee on Animal Resources at the University of Rochester.

2.3. Statistical analyses

Statistical analyses were performed using PASW Statistics 18.0.2 (SPSS Inc., Chicago IL, USA). When comparing two data sets, Pearson correlation coefficients were calculated and paired t-tests were performed. A one-way t-test was used to compare a mean to a constant value. In addition, a one-way analysis of variance (ANOVA) was used to test the relationship between cone spacing and retinal eccentricity. Differences were deemed significant when p ≤ 0.05.

2.4. Ex vivo two-photon imaging of macaque retina

Immediately after a macaque (macaca fascicularis) was euthanized with anesthetic (Sleepaway, Fort Dodge Animal Health, Fort Dodge, IA, USA), the eyes were enucleated and maintained in carbogenated (95% O2 and 5% CO2) Ames' medium (Sigma, St. Louis, MO, USA), containing sodium bicarbonate (1.9 g/L) and glucose (0.8 g/L), and kept on ice. Except for a short period (approximately 10 minutes), when the tissue was moved to the imaging facility, the Ames’ medium was continuously bubbled with carbogen. At room temperature and under dim red light, a small piece of the central retina with RPE and choroid attached was dissected and flattened onto a membrane filter with the ganglion cells facing up.

The retinal preparation in Ames’ medium was imaged at room temperature by using a two-photon microscope (Olympus FluoView 1000 AOM-MPM system, Center Valley, PA, USA) at 100x, with an objective of 1.05 NA (Olympus, Center Valley, PA, USA) for up to 3 hours. The Ames’ medium was not bubbled with carbogen during imaging. The microscope was set-up to mimic in vivo excitation and emission spectra. Image stacks in whole-mount views covering the depth of the photoreceptor layer were acquired in both the original pre-bleached state, having been exposed only to dim red light, and then the post-bleached state, after a 2 minute exposure to blue (488 nm) light. The x, y and z pixel sizes of the image stacks were 0.124 μm, 0.124 μm and 0.25 μm, respectively. The time to acquire a single pixel was 2 μs with Kalman 3 line averaging.

3. Results

3.1. In vivo two-photon images of the photoreceptor mosaic

To our knowledge, this is the first demonstration of two-photon excited fluorescence imaging of a living primate eye. In vivo two-photon excited fluorescence images of macaque retina revealed a regular array of spots (Fig. 2a
Fig. 2 Images of the cone mosaic in the living primate retina. At 2.5° superior, (a) the two-photon image and (b) the reflectance image show good correspondence. The cross correlation coefficient between these images is 0.9. In magnified sections (c) of the larger images, denoted by white rectangles in (a) and (b), the correspondence between individual cones can be observed (white arrows). Black arrows indicate a cone that was not reflecting light but shows a strong fluorescence signal. The images in (c) were low pass filtered to remove frequencies above the diffraction-limit, thereby improving cone visibility. Scale bars, 50 μm. The quadratic nature of the emitted fluorescence as a function of incident excitation power is shown (d). Error bars represent the standard error of the mean gray level among individual frames.
) that correspond to the locations of cone photoreceptors imaged simultaneously by reflected near infrared light (Fig. 2b). Emission from two-photon excited fluorescence, rather than single photon fluorescence, was confirmed by several criteria: (1) the emitted power was a quadratic function of the excitation power (i.e. the mean power series exponent did not differ significantly from 2 by 1-way t-test; n = 8; α = 0.05; p = 0.06) (Fig. 2d), (2) dispersion compensation increased fluorescence emission, and (3) the emission wavelengths were shorter than the excitation wavelength. Two-photon signals were weak; a single two-photon excited fluorescence frame had 0.0002 – 0.0007 photons per pixel. The processed images, obtained by summing 16,500 frames, had a mean value of approximately 12 photons per pixel. The two-photon fluorescence emission originated from the cone photoreceptors because, with rare exceptions, each bright spot in the two-photon images (Fig. 2a-c) had a corresponding spot at the same location in the reflectance images of the cone mosaic. Moreover, this correspondence held at every eccentricity we studied (Fig. 3a-c
Fig. 3 Mean cone spacing with eccentricity verifies that two-photon fluorescence originates from the cone mosaic. Shown are two-photon images of the cone mosaic in the living primate at three eccentricities in superior retina, (a) 5.5°, (b) 9.1° and (c) 13°. Scale bars, 50 μm. Cone spacing, as determined in Fourier space, is shown as a function of eccentricity (d) from two-photon (●) and reflectance (Δ) images. Error bars represent the width of the secondary peak in the Fourier spectra.
). In some cases, cones that were not waveguiding light in the reflectance image, and hence may have been considered missing, were visible in the fluorescence image, indicating that they were probably viable cells (Fig. 2c). According to a paired t-test, the spacing of the cones and the spacing of the two-photon imaging spots, each determined from the Fourier spectra of the images, were not significantly different (n = 7; α = 0.05; p = 0.40) and both increased with eccentricity in a manner unique to the cone mosaic among cell classes in the primate retina (Fig. 3d). Although there is evidence for some fluorescence from rods, they were not clearly identifiable.

3.2. Ex vivo two-photon images of the photoreceptor mosaic

3.3. In vivo functional measurements

In the living macaque eye, we observed that fluorescence emission increased in response to photoreceptor bleaching, as measured by the mean gray level of each two-photon fluorescence frame (Fig. 5
Fig. 5 Fluorescence emission response during photoreceptor bleaching. The results for three different retinal locations are shown. Data points are the means of 2 s time intervals and error bars represent the standard error of the means. Lines represent the best fits to the unbinned data.
). This is consistent with ex vivo observations. Because of differences in cone density and vasculature, the magnitude of the increase in fluorescence varies with location from 1.3 to 2 times. The time constants for a 1/e increase ranged from 7 s to 32 s, longer than expected for cone bleaching (2 s). The measured changes in fluorescence can indicate increases in imaged fluorophore concentration.

4. Discussion

These results demonstrate that it is possible to image cellular structures in the living primate eye with two-photon fluorescence. The specific fluorophore(s) that were excited remain(s) to be determined. Fluorophores previously imaged in ex vivo photoreceptors have included mitochondrial flavin adenine dinucleotide (FAD) [15

15. E. J. Gualda, J. M. Bueno, and P. Artal, “Wavefront optimized nonlinear microscopy of ex vivo human retinas,” J. Biomed. Opt. 15(2), 026007 (2010). [CrossRef] [PubMed]

,16

16. L. Zhao, J. Qu, and H. Niu, “Identification of endogenous fluorophores in the photoreceptors using autofluorescence spectroscopy,” in Optics in Health Care and Biomedical Optics III, X. Li, Q. Luo, and Y. Gu, eds. (SPIE, 2007).

], reduced pyridine nucleotides involved in cellular metabolism (NADH and NADPH, collectively referred to as NAD(P)H) [6

6. C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]

,13

13. M. Han, G. Giese, S. Schmitz-Valckenberg, A. Bindewald-Wittich, F. G. Holz, J. Yu, J. F. Bille, and M. H. Niemz, “Age-related structural abnormalities in the human retina-choroid complex revealed by two-photon excited autofluorescence imaging,” J. Biomed. Opt. 12(2), 024012 (2007). [CrossRef] [PubMed]

,15

15. E. J. Gualda, J. M. Bueno, and P. Artal, “Wavefront optimized nonlinear microscopy of ex vivo human retinas,” J. Biomed. Opt. 15(2), 026007 (2010). [CrossRef] [PubMed]

], A2-PE [16

16. L. Zhao, J. Qu, and H. Niu, “Identification of endogenous fluorophores in the photoreceptors using autofluorescence spectroscopy,” in Optics in Health Care and Biomedical Optics III, X. Li, Q. Luo, and Y. Gu, eds. (SPIE, 2007).

] and all-trans-retinol [6

6. C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]

,13

13. M. Han, G. Giese, S. Schmitz-Valckenberg, A. Bindewald-Wittich, F. G. Holz, J. Yu, J. F. Bille, and M. H. Niemz, “Age-related structural abnormalities in the human retina-choroid complex revealed by two-photon excited autofluorescence imaging,” J. Biomed. Opt. 12(2), 024012 (2007). [CrossRef] [PubMed]

,15

15. E. J. Gualda, J. M. Bueno, and P. Artal, “Wavefront optimized nonlinear microscopy of ex vivo human retinas,” J. Biomed. Opt. 15(2), 026007 (2010). [CrossRef] [PubMed]

,17

17. R. C. Sears and M. W. Kaplan, “Axial diffusion of retinol in isolated frog rod outer segments following substantial bleaches of visual pigment,” Vision Res. 29(11), 1485–1492 (1989). [CrossRef] [PubMed]

]. Because A2-PE and all-trans-retinol are products of the visual cycle that are predominately located in outer segments, substantial amounts would not be expected in cone inner segments. Fluorophores in cone inner segments can also include 11-cis-retinol [18

18. J. S. Wang and V. J. Kefalov, “An alternative pathway mediates the mouse and human cone visual cycle,” Curr. Biol. 19(19), 1665–1669 (2009). [CrossRef] [PubMed]

] or compounds yet to be identified.

Because of the low number of emitted fluorescent photons, it is not currently possible to experimentally identify in vivo fluorophores using the FAOSLO. NAD(P)H and retinol have similar two-photon excitation cross-sections [19

19. W. R. Zipfel, R. M. Williams, R. Christie, A. Y. Nikitin, B. T. Hyman, and W. W. Webb, “Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7075–7080 (2003). [CrossRef] [PubMed]

]. At 730 nm, the wavelength used for fluorescence excitation, the two-photon cross-section of FAD is almost double that of NAD(P)H, but follows a similar action spectrum until it peaks again near 900 nm [20

20. S. Huang, A. A. Heikal, and W. W. Webb, “Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein,” Biophys. J. 82(5), 2811–2825 (2002). [CrossRef] [PubMed]

]. Although the emission peaks [6

6. C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]

,19

19. W. R. Zipfel, R. M. Williams, R. Christie, A. Y. Nikitin, B. T. Hyman, and W. W. Webb, “Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7075–7080 (2003). [CrossRef] [PubMed]

,20

20. S. Huang, A. A. Heikal, and W. W. Webb, “Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein,” Biophys. J. 82(5), 2811–2825 (2002). [CrossRef] [PubMed]

] are slightly separated, NAD(P)H, FAD and retinol are all easily detected by the broad emission collection in the FAOSLO. Given their spectral properties, emission from other fluorophores, such as A2-PE [16

16. L. Zhao, J. Qu, and H. Niu, “Identification of endogenous fluorophores in the photoreceptors using autofluorescence spectroscopy,” in Optics in Health Care and Biomedical Optics III, X. Li, Q. Luo, and Y. Gu, eds. (SPIE, 2007).

] or lipofuscin [21

21. F. C. Delori, C. K. Dorey, G. Staurenghi, O. Arend, D. G. Goger, and J. J. Weiter, “In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics,” Invest. Ophthalmol. Vis. Sci. 36(3), 718–729 (1995). [PubMed]

], is unlikely to be collected in significant quantities.

In vivo two-photon imaging was achieved without observable retinal damage as assessed from 1 day to a year later by fundus photography and fluorescein angiography. Moreover, the same location could be imaged on separate occasions with no detectable change in the appearance of the fluorescence or reflectance images. If this method were to be used in humans, the light levels required would have to comply with the current American National Standard for the Safe Use of Lasers [22

22. American National Standards Institute, American National Standard for Safe Use of Lasers (American National Standards Institute, Laser Institute of America, 2007).

] which provides guidance for calculating maximum permissible exposures (MPEs) for ocular light incorporating about an order of magnitude of safety. MPE calculations for a scanning laser ophthalmoscope have been described in detail elsewhere [4

4. J. I. Morgan, J. J. Hunter, B. Masella, R. Wolfe, D. C. Gray, W. H. Merigan, F. C. Delori, and D. R. Williams, “Light-induced retinal changes observed with high-resolution autofluorescence imaging of the retinal pigment epithelium,” Invest. Ophthalmol. Vis. Sci. 49(8), 3715–3729 (2008). [CrossRef] [PubMed]

,23

23. F. C. Delori, R. H. Webb, and D. H. SlineyF. C. DeloriR. H. WebbD. H. SlineyAmerican National Standards Institute, “Maximum permissible exposures for ocular safety (ANSI 2000), with emphasis on ophthalmic devices,” J. Opt. Soc. Am. A 24(5), 1250–1265 (2007). [CrossRef] [PubMed]

]. For the FAOSLO, with imaging conditions described herein, the MPE is 665 μW for a 12 minute exposure (the acquisition time for generating a single two-photon image). Successful in vivo two-photon imaging was achieved by using 3 to 3.5 mW of excitation power incident on the cornea, over 4.5 times the 12 minute ANSI MPE, but less than the damage threshold expected from experimental data for continuous wave illumination [24

24. W. T. Ham Jr, H. A. Mueller, J. J. Ruffolo Jr, and A. M. Clarke, “Sensitivity of the retina to radiation damage as a function of wavelength,” Photochem. Photobiol. 29(4), 735–743 (1979). [CrossRef] [PubMed]

], a suitable comparison for thermal damage. With improvements in light efficiency, safe two-photon imaging of the living human eye appears to be feasible.

In vivo imaging can provide insight into the molecular changes that occur during the phototransduction cascade and subsequent visual pigment regeneration. Improved understanding of the processes of vision in living healthy and diseased retina can help advance therapies for successful aging, as well as improve the diagnosis and treatment of some retinal pathologies [2

2. G. H. Travis, M. Golczak, A. R. Moise, and K. Palczewski, “Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents,” Annu. Rev. Pharmacol. Toxicol. 47(1), 469–512 (2007). [CrossRef] [PubMed]

]. Intrinsic signals have been investigated in vivo at low spatial resolution with a fundus camera [25

25. D. Ts’o, J. Schallek, Y. Kwon, R. Kardon, M. Abramoff, and P. Soliz, “Noninvasive functional imaging of the retina reveals outer retinal and hemodynamic intrinsic optical signal origins,” Jpn. J. Ophthalmol. 53(4), 334–344 (2009). [CrossRef] [PubMed]

,26

26. K. Tsunoda, G. Hanazono, K. Inomata, Y. Kazato, W. Suzuki, and M. Tanifuji, “Origins of retinal intrinsic signals: a series of experiments on retinas of macaque monkeys,” Jpn. J. Ophthalmol. 53(4), 297–314 (2009). [CrossRef] [PubMed]

] and at the cellular scale with OCT [27

27. V. J. Srinivasan, Y. Chen, J. S. Duker, and J. G. Fujimoto, “In vivo functional imaging of intrinsic scattering changes in the human retina with high-speed ultrahigh resolution OCT,” Opt. Express 17(5), 3861–3877 (2009). [CrossRef] [PubMed]

], an AOSLO [28

28. K. Grieve and A. Roorda, “Intrinsic signals from human cone photoreceptors,” Invest. Ophthalmol. Vis. Sci. 49(2), 713–719 (2008). [CrossRef] [PubMed]

] and an AO flood-illuminated camera [29

29. R. S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, and D. T. Miller, “In vivo functional imaging of human cone photoreceptors,” Opt. Express 15(24), 16141–16160 (2007). [CrossRef]

]. In response to visible light stimuli, positive and negative changes in near-infrared reflectance have been observed, the origins of which are not completely understood. The observed intrinsic signals have been attributed to changes in vascular blood flow [25

25. D. Ts’o, J. Schallek, Y. Kwon, R. Kardon, M. Abramoff, and P. Soliz, “Noninvasive functional imaging of the retina reveals outer retinal and hemodynamic intrinsic optical signal origins,” Jpn. J. Ophthalmol. 53(4), 334–344 (2009). [CrossRef] [PubMed]

] and/or photoreceptor changes such as, membrane hyperpolarisation [26

26. K. Tsunoda, G. Hanazono, K. Inomata, Y. Kazato, W. Suzuki, and M. Tanifuji, “Origins of retinal intrinsic signals: a series of experiments on retinas of macaque monkeys,” Jpn. J. Ophthalmol. 53(4), 297–314 (2009). [CrossRef] [PubMed]

,28

28. K. Grieve and A. Roorda, “Intrinsic signals from human cone photoreceptors,” Invest. Ophthalmol. Vis. Sci. 49(2), 713–719 (2008). [CrossRef] [PubMed]

,29

29. R. S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, and D. T. Miller, “In vivo functional imaging of human cone photoreceptors,” Opt. Express 15(24), 16141–16160 (2007). [CrossRef]

], cell swelling [26

26. K. Tsunoda, G. Hanazono, K. Inomata, Y. Kazato, W. Suzuki, and M. Tanifuji, “Origins of retinal intrinsic signals: a series of experiments on retinas of macaque monkeys,” Jpn. J. Ophthalmol. 53(4), 297–314 (2009). [CrossRef] [PubMed]

,28

28. K. Grieve and A. Roorda, “Intrinsic signals from human cone photoreceptors,” Invest. Ophthalmol. Vis. Sci. 49(2), 713–719 (2008). [CrossRef] [PubMed]

,29

29. R. S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, and D. T. Miller, “In vivo functional imaging of human cone photoreceptors,” Opt. Express 15(24), 16141–16160 (2007). [CrossRef]

], and changes in refractive index or scattering properties [29

29. R. S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, and D. T. Miller, “In vivo functional imaging of human cone photoreceptors,” Opt. Express 15(24), 16141–16160 (2007). [CrossRef]

]. These are indirect measures of the effects of chemical changes occurring in response to photoreceptor activation. Two-photon imaging of the living eye at a cellular scale has the potential to directly measure the changes in concentrations of fluorescent molecules involved in visual excitation. Using two-photon imaging in an isolated frog rod, Chen and colleagues [6

6. C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]

] demonstrated an increase in the two-photon excited fluorescence signal following exposure to visible light. Spectroscopic measurements identified the fluorophores as NAD(P)H in the rod inner segments and all-trans-retinol in the outer segments. They also obtained similar results with isolated mouse retina. Here, we have shown, in vivo and in an ex vivo preparation, an increase in two-photon fluorescence signal from cone inner segments in response to light exposures that would result in cone bleaching.

When enabled by a high-resolution adaptive optics scanning laser ophthalmoscope, two-photon imaging provides functional measurements at the cellular scale in the living eye. The nature of current functional measurements is still under investigation. The increased fluorescence may represent the creation of new fluorescent molecules or an increase in the concentration of existing fluorescent molecules either directly by the two-photon excitation light or by its stimulation of a visual response. The capability to image changes in cellular metabolism (if imaging FAD or NAD(P)H) or the influx and conversion of 11-cis-retinol in cone inner segments in response to visual stimuli is of interest, not only in young and aging healthy eyes, but also in eyes with retinal pathology. If the two-photon imaging signal emanates from NAD(P)H or FAD, mitochondrial dysfunction, such as that originating from Leber’s hereditary optic neuropathy [30

30. P. Y. Man, D. M. Turnbull, and P. F. Chinnery, “Leber hereditary optic neuropathy,” J. Med. Genet. 39(3), 162–169 (2002). [CrossRef] [PubMed]

] or NARP (neurogenic muscle weakness, ataxia, retinitis pigmentosa) [31

31. I. J. Holt, A. E. Harding, R. K. Petty, and J. A. Morgan-Hughes, “A new mitochondrial disease associated with mitochondrial DNA heteroplasmy,” Am. J. Hum. Genet. 46(3), 428–433 (1990). [PubMed]

], the technique can display different fluorescence changes over time when compared to normal healthy eyes. Altered responses to light may also be observed with diseases of the visual cycle, including Leber’s congenital amaurosis and Stargardt disease [2

2. G. H. Travis, M. Golczak, A. R. Moise, and K. Palczewski, “Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents,” Annu. Rev. Pharmacol. Toxicol. 47(1), 469–512 (2007). [CrossRef] [PubMed]

]. Two-photon fluorescence imaging capabilities could be highly useful for monitoring the efficacy of proposed therapies.

5. Conclusions

With the use of an adaptive optics scanning laser ophthalmoscope with dual imaging capabilities, the many challenges for in vivo two-photon fluorescence imaging were overcome to produce the first two-photon fluorescence images of the living primate retina. Images were obtained with light levels that did not produce observable retinal damage. Although the specific fluorophore is as yet unknown, a strong in vivo fluorescence signal originates from cone inner segments producing images of the cone mosaic and providing functional measurements of an early stage in the visual process. Future applications of two-photon fluorescence imaging in the primate eye may also include the use of extrinsic fluorophores.

Acknowledgments

For their assistance with this research, we thank Kamran Ahmad, John Moonan, Jennifer Norris, Lee Anne Schery and Robert Wolfe. Ex vivo two-photon imaging was performed at the Multiphoton Core Facility at the University of Rochester Medical Center with the assistance of Karl Kasischke, Gheorghe Salahura and Anita Sun. We appreciate financial support from the following sources: Polgenix, Inc.; National Institute for Health, Bethesda, Maryland Grants P30-EY001319, R01-EY004367, BRP-EY014375, T32-EY007125, R01-EY009339, R24-EY021126, R43-EY020715. This work made use of STC shared experimental facilities supported by the NSF under Agreement No. AST-9876783, Research to Prevent Blindness. Alfredo Dubra-Suarez, Ph.D., holds a Career Award at the Scientific Interface from the Burroughs Welcome Fund; Klaus Tschira Foundation Heidelberg, Germany; European Life Scientist Organization; TECH 09-004 State of Ohio Department of Development; Third Frontier Commission. DeMotion image registration software was developed by Alfredo Dubra and Zach Harvey with funding from Research to Prevent Blindness and the National Institute of Health, Bethesda, Maryland through the grants BRP-EY014375 and 5 K23 EY016700. Adaptive optics control software was developed by Alfredo Dubra and Kamran Ahmad.

References and Links

1.

T. D. Lamb and E. N. Pugh Jr., “Dark adaptation and the retinoid cycle of vision,” Prog. Retin. Eye Res. 23(3), 307–380 (2004). [CrossRef] [PubMed]

2.

G. H. Travis, M. Golczak, A. R. Moise, and K. Palczewski, “Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents,” Annu. Rev. Pharmacol. Toxicol. 47(1), 469–512 (2007). [CrossRef] [PubMed]

3.

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. Express 14(16), 7144–7158 (2006). [CrossRef] [PubMed]

4.

J. I. Morgan, J. J. Hunter, B. Masella, R. Wolfe, D. C. Gray, W. H. Merigan, F. C. Delori, and D. R. Williams, “Light-induced retinal changes observed with high-resolution autofluorescence imaging of the retinal pigment epithelium,” Invest. Ophthalmol. Vis. Sci. 49(8), 3715–3729 (2008). [CrossRef] [PubMed]

5.

J. I. Morgan, A. Dubra, R. Wolfe, W. H. Merigan, and D. R. Williams, “In vivo autofluorescence imaging of the human and macaque retinal pigment epithelial cell mosaic,” Invest. Ophthalmol. Vis. Sci. 50(3), 1350–1359 (2008). [CrossRef] [PubMed]

6.

C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]

7.

J. Dillon, L. Zheng, J. C. Merriam, and E. R. Gaillard, “Transmission spectra of light to the mammalian retina,” Photochem. Photobiol. 71(2), 225–229 (2000). [CrossRef] [PubMed]

8.

A. Dubra and Z. Harvey, “Registration of 2D images from fast scanning ophthalmic instruments” presented at WBIR 2010—Workshop on Biomedical Image Registration, July 11–13 2010, Lübeck, Germany.

9.

G. Wyszecki, and W. S. Stiles, Color Science: Concepts and Methods, Quantitative Data and Formulae (John Wiley & Sons, Inc., 1982).

10.

Y. Imanishi, M. L. Batten, D. W. Piston, W. Baehr, and K. Palczewski, “Noninvasive two-photon imaging reveals retinyl ester storage structures in the eye,” J. Cell Biol. 164(3), 373–383 (2004). [CrossRef] [PubMed]

11.

M. Han, A. Bindewald-Wittich, F. G. Holz, G. Giese, M. H. Niemz, S. Snyder, H. Sun, J. Yu, M. Agopov, O. La Schiazza, and J. F. Bille, “Two-photon excited autofluorescence imaging of human retinal pigment epithelial cells,” J. Biomed. Opt. 11(1), 010501 (2006). [CrossRef] [PubMed]

12.

A. Bindewald-Wittich, M. Han, S. Schmitz-Valckenberg, S. R. Snyder, G. Giese, J. F. Bille, and F. G. Holz, “Two-photon-excited fluorescence imaging of human RPE cells with a femtosecond Ti:sapphire laser,” Invest. Ophthalmol. Vis. Sci. 47(10), 4553–4557 (2006). [CrossRef] [PubMed]

13.

M. Han, G. Giese, S. Schmitz-Valckenberg, A. Bindewald-Wittich, F. G. Holz, J. Yu, J. F. Bille, and M. H. Niemz, “Age-related structural abnormalities in the human retina-choroid complex revealed by two-photon excited autofluorescence imaging,” J. Biomed. Opt. 12(2), 024012 (2007). [CrossRef] [PubMed]

14.

O. La Schiazza and J. F. Bille, “High-speed two-photon excited autofluorescence imaging of ex vivo human retinal pigment epithelial cells toward age-related macular degeneration diagnostic,” J. Biomed. Opt. 13(6), 064008 (2008). [CrossRef] [PubMed]

15.

E. J. Gualda, J. M. Bueno, and P. Artal, “Wavefront optimized nonlinear microscopy of ex vivo human retinas,” J. Biomed. Opt. 15(2), 026007 (2010). [CrossRef] [PubMed]

16.

L. Zhao, J. Qu, and H. Niu, “Identification of endogenous fluorophores in the photoreceptors using autofluorescence spectroscopy,” in Optics in Health Care and Biomedical Optics III, X. Li, Q. Luo, and Y. Gu, eds. (SPIE, 2007).

17.

R. C. Sears and M. W. Kaplan, “Axial diffusion of retinol in isolated frog rod outer segments following substantial bleaches of visual pigment,” Vision Res. 29(11), 1485–1492 (1989). [CrossRef] [PubMed]

18.

J. S. Wang and V. J. Kefalov, “An alternative pathway mediates the mouse and human cone visual cycle,” Curr. Biol. 19(19), 1665–1669 (2009). [CrossRef] [PubMed]

19.

W. R. Zipfel, R. M. Williams, R. Christie, A. Y. Nikitin, B. T. Hyman, and W. W. Webb, “Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7075–7080 (2003). [CrossRef] [PubMed]

20.

S. Huang, A. A. Heikal, and W. W. Webb, “Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein,” Biophys. J. 82(5), 2811–2825 (2002). [CrossRef] [PubMed]

21.

F. C. Delori, C. K. Dorey, G. Staurenghi, O. Arend, D. G. Goger, and J. J. Weiter, “In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics,” Invest. Ophthalmol. Vis. Sci. 36(3), 718–729 (1995). [PubMed]

22.

American National Standards Institute, American National Standard for Safe Use of Lasers (American National Standards Institute, Laser Institute of America, 2007).

23.

F. C. Delori, R. H. Webb, and D. H. SlineyF. C. DeloriR. H. WebbD. H. SlineyAmerican National Standards Institute, “Maximum permissible exposures for ocular safety (ANSI 2000), with emphasis on ophthalmic devices,” J. Opt. Soc. Am. A 24(5), 1250–1265 (2007). [CrossRef] [PubMed]

24.

W. T. Ham Jr, H. A. Mueller, J. J. Ruffolo Jr, and A. M. Clarke, “Sensitivity of the retina to radiation damage as a function of wavelength,” Photochem. Photobiol. 29(4), 735–743 (1979). [CrossRef] [PubMed]

25.

D. Ts’o, J. Schallek, Y. Kwon, R. Kardon, M. Abramoff, and P. Soliz, “Noninvasive functional imaging of the retina reveals outer retinal and hemodynamic intrinsic optical signal origins,” Jpn. J. Ophthalmol. 53(4), 334–344 (2009). [CrossRef] [PubMed]

26.

K. Tsunoda, G. Hanazono, K. Inomata, Y. Kazato, W. Suzuki, and M. Tanifuji, “Origins of retinal intrinsic signals: a series of experiments on retinas of macaque monkeys,” Jpn. J. Ophthalmol. 53(4), 297–314 (2009). [CrossRef] [PubMed]

27.

V. J. Srinivasan, Y. Chen, J. S. Duker, and J. G. Fujimoto, “In vivo functional imaging of intrinsic scattering changes in the human retina with high-speed ultrahigh resolution OCT,” Opt. Express 17(5), 3861–3877 (2009). [CrossRef] [PubMed]

28.

K. Grieve and A. Roorda, “Intrinsic signals from human cone photoreceptors,” Invest. Ophthalmol. Vis. Sci. 49(2), 713–719 (2008). [CrossRef] [PubMed]

29.

R. S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, and D. T. Miller, “In vivo functional imaging of human cone photoreceptors,” Opt. Express 15(24), 16141–16160 (2007). [CrossRef]

30.

P. Y. Man, D. M. Turnbull, and P. F. Chinnery, “Leber hereditary optic neuropathy,” J. Med. Genet. 39(3), 162–169 (2002). [CrossRef] [PubMed]

31.

I. J. Holt, A. E. Harding, R. K. Petty, and J. A. Morgan-Hughes, “A new mitochondrial disease associated with mitochondrial DNA heteroplasmy,” Am. J. Hum. Genet. 46(3), 428–433 (1990). [PubMed]

OCIS Codes
(010.1080) Atmospheric and oceanic optics : Active or adaptive optics
(330.4460) Vision, color, and visual optics : Ophthalmic optics and devices
(330.5310) Vision, color, and visual optics : Vision - photoreceptors
(330.7327) Vision, color, and visual optics : Visual optics, ophthalmic instrumentation

ToC Category:
Ophthalmology Applications

History
Original Manuscript: November 8, 2010
Revised Manuscript: December 14, 2010
Manuscript Accepted: December 14, 2010
Published: December 17, 2010

Citation
Jennifer J. Hunter, Benjamin Masella, Alfredo Dubra, Robin Sharma, Lu Yin, William H. Merigan, Grazyna Palczewska, Krzysztof Palczewski, and David R. Williams, "Images of photoreceptors in living primate eyes using adaptive optics two-photon ophthalmoscopy," Biomed. Opt. Express 2, 139-148 (2011)
http://www.opticsinfobase.org/boe/abstract.cfm?URI=boe-2-1-139


Sort:  Author  |  Year  |  Journal  |  Reset  

References

  1. T. D. Lamb and E. N. Pugh., “Dark adaptation and the retinoid cycle of vision,” Prog. Retin. Eye Res. 23(3), 307–380 (2004). [CrossRef] [PubMed]
  2. G. H. Travis, M. Golczak, A. R. Moise, and K. Palczewski, “Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents,” Annu. Rev. Pharmacol. Toxicol. 47(1), 469–512 (2007). [CrossRef] [PubMed]
  3. 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. Express 14(16), 7144–7158 (2006). [CrossRef] [PubMed]
  4. J. I. Morgan, J. J. Hunter, B. Masella, R. Wolfe, D. C. Gray, W. H. Merigan, F. C. Delori, and D. R. Williams, “Light-induced retinal changes observed with high-resolution autofluorescence imaging of the retinal pigment epithelium,” Invest. Ophthalmol. Vis. Sci. 49(8), 3715–3729 (2008). [CrossRef] [PubMed]
  5. J. I. Morgan, A. Dubra, R. Wolfe, W. H. Merigan, and D. R. Williams, “In vivo autofluorescence imaging of the human and macaque retinal pigment epithelial cell mosaic,” Invest. Ophthalmol. Vis. Sci. 50(3), 1350–1359 (2008). [CrossRef] [PubMed]
  6. C. Chen, E. Tsina, M. C. Cornwall, R. K. Crouch, S. Vijayaraghavan, and Y. Koutalos, “Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors,” Biophys. J. 88(3), 2278–2287 (2005). [CrossRef] [PubMed]
  7. J. Dillon, L. Zheng, J. C. Merriam, and E. R. Gaillard, “Transmission spectra of light to the mammalian retina,” Photochem. Photobiol. 71(2), 225–229 (2000). [CrossRef] [PubMed]
  8. A. Dubra and Z. Harvey, “Registration of 2D images from fast scanning ophthalmic instruments” presented at WBIR 2010—Workshop on Biomedical Image Registration, July 11–13 2010, Lübeck, Germany.
  9. G. Wyszecki, and W. S. Stiles, Color Science: Concepts and Methods, Quantitative Data and Formulae (John Wiley & Sons, Inc., 1982).
  10. Y. Imanishi, M. L. Batten, D. W. Piston, W. Baehr, and K. Palczewski, “Noninvasive two-photon imaging reveals retinyl ester storage structures in the eye,” J. Cell Biol. 164(3), 373–383 (2004). [CrossRef] [PubMed]
  11. M. Han, A. Bindewald-Wittich, F. G. Holz, G. Giese, M. H. Niemz, S. Snyder, H. Sun, J. Yu, M. Agopov, O. La Schiazza, and J. F. Bille, “Two-photon excited autofluorescence imaging of human retinal pigment epithelial cells,” J. Biomed. Opt. 11(1), 010501 (2006). [CrossRef] [PubMed]
  12. A. Bindewald-Wittich, M. Han, S. Schmitz-Valckenberg, S. R. Snyder, G. Giese, J. F. Bille, and F. G. Holz, “Two-photon-excited fluorescence imaging of human RPE cells with a femtosecond Ti:sapphire laser,” Invest. Ophthalmol. Vis. Sci. 47(10), 4553–4557 (2006). [CrossRef] [PubMed]
  13. M. Han, G. Giese, S. Schmitz-Valckenberg, A. Bindewald-Wittich, F. G. Holz, J. Yu, J. F. Bille, and M. H. Niemz, “Age-related structural abnormalities in the human retina-choroid complex revealed by two-photon excited autofluorescence imaging,” J. Biomed. Opt. 12(2), 024012 (2007). [CrossRef] [PubMed]
  14. O. La Schiazza and J. F. Bille, “High-speed two-photon excited autofluorescence imaging of ex vivo human retinal pigment epithelial cells toward age-related macular degeneration diagnostic,” J. Biomed. Opt. 13(6), 064008 (2008). [CrossRef] [PubMed]
  15. E. J. Gualda, J. M. Bueno, and P. Artal, “Wavefront optimized nonlinear microscopy of ex vivo human retinas,” J. Biomed. Opt. 15(2), 026007 (2010). [CrossRef] [PubMed]
  16. L. Zhao, J. Qu, and H. Niu, “Identification of endogenous fluorophores in the photoreceptors using autofluorescence spectroscopy,” in Optics in Health Care and Biomedical Optics III, X. Li, Q. Luo, and Y. Gu, eds. (SPIE, 2007).
  17. R. C. Sears and M. W. Kaplan, “Axial diffusion of retinol in isolated frog rod outer segments following substantial bleaches of visual pigment,” Vision Res. 29(11), 1485–1492 (1989). [CrossRef] [PubMed]
  18. J. S. Wang and V. J. Kefalov, “An alternative pathway mediates the mouse and human cone visual cycle,” Curr. Biol. 19(19), 1665–1669 (2009). [CrossRef] [PubMed]
  19. W. R. Zipfel, R. M. Williams, R. Christie, A. Y. Nikitin, B. T. Hyman, and W. W. Webb, “Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation,” Proc. Natl. Acad. Sci. U.S.A. 100(12), 7075–7080 (2003). [CrossRef] [PubMed]
  20. S. Huang, A. A. Heikal, and W. W. Webb, “Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein,” Biophys. J. 82(5), 2811–2825 (2002). [CrossRef] [PubMed]
  21. F. C. Delori, C. K. Dorey, G. Staurenghi, O. Arend, D. G. Goger, and J. J. Weiter, “In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics,” Invest. Ophthalmol. Vis. Sci. 36(3), 718–729 (1995). [PubMed]
  22. American National Standards Institute, American National Standard for Safe Use of Lasers (American National Standards Institute, Laser Institute of America, 2007).
  23. F. C. Delori, R. H. Webb, D. H. Sliney, and American National Standards Institute, “Maximum permissible exposures for ocular safety (ANSI 2000), with emphasis on ophthalmic devices,” J. Opt. Soc. Am. A 24(5), 1250–1265 (2007). [CrossRef] [PubMed]
  24. W. T. Ham, H. A. Mueller, J. J. Ruffolo, and A. M. Clarke, “Sensitivity of the retina to radiation damage as a function of wavelength,” Photochem. Photobiol. 29(4), 735–743 (1979). [CrossRef] [PubMed]
  25. D. Ts’o, J. Schallek, Y. Kwon, R. Kardon, M. Abramoff, and P. Soliz, “Noninvasive functional imaging of the retina reveals outer retinal and hemodynamic intrinsic optical signal origins,” Jpn. J. Ophthalmol. 53(4), 334–344 (2009). [CrossRef] [PubMed]
  26. K. Tsunoda, G. Hanazono, K. Inomata, Y. Kazato, W. Suzuki, and M. Tanifuji, “Origins of retinal intrinsic signals: a series of experiments on retinas of macaque monkeys,” Jpn. J. Ophthalmol. 53(4), 297–314 (2009). [CrossRef] [PubMed]
  27. V. J. Srinivasan, Y. Chen, J. S. Duker, and J. G. Fujimoto, “In vivo functional imaging of intrinsic scattering changes in the human retina with high-speed ultrahigh resolution OCT,” Opt. Express 17(5), 3861–3877 (2009). [CrossRef] [PubMed]
  28. K. Grieve and A. Roorda, “Intrinsic signals from human cone photoreceptors,” Invest. Ophthalmol. Vis. Sci. 49(2), 713–719 (2008). [CrossRef] [PubMed]
  29. R. S. Jonnal, J. Rha, Y. Zhang, B. Cense, W. Gao, and D. T. Miller, “In vivo functional imaging of human cone photoreceptors,” Opt. Express 15(24), 16141–16160 (2007). [CrossRef]
  30. P. Y. Man, D. M. Turnbull, and P. F. Chinnery, “Leber hereditary optic neuropathy,” J. Med. Genet. 39(3), 162–169 (2002). [CrossRef] [PubMed]
  31. I. J. Holt, A. E. Harding, R. K. Petty, and J. A. Morgan-Hughes, “A new mitochondrial disease associated with mitochondrial DNA heteroplasmy,” Am. J. Hum. Genet. 46(3), 428–433 (1990). [PubMed]

Cited By

Alert me when this paper is cited

OSA is able to provide readers links to articles that cite this paper by participating in CrossRef's Cited-By Linking service. CrossRef includes content from more than 3000 publishers and societies. In addition to listing OSA journal articles that cite this paper, citing articles from other participating publishers will also be listed.

Figures

Fig. 1 Fig. 2 Fig. 3
 
Fig. 4 Fig. 5
 

« Previous Article  |  Next Article »

OSA is a member of CrossRef.

CrossCheck Deposited