Formation and Clearance of All-Trans-Retinol in Rods Investigated in the Living Primate Eye With Two-Photon Ophthalmoscopy

Purpose Two-photon excited fluorescence (TPEF) imaging has potential as a functional tool for tracking visual pigment regeneration in the living eye. Previous studies have shown that all-trans-retinol is likely the chief source of time-varying TPEF from photoreceptors. Endogenous TPEF from retinol could provide the specificity desired for tracking the visual cycle. However, in vivo characterization of native retinol kinetics is complicated by visual stimulation from the imaging beam. We have developed an imaging scheme for overcoming these challenges and monitored the formation and clearance of retinol. Methods Three macaques were imaged by using an in vivo two-photon ophthalmoscope. Endogenous TPEF was excited at 730 nm and recorded through the eye's pupil for more than 90 seconds. Two-photon excited fluorescence increased with onset of light and plateaued within 40 seconds, at which point, brief incremental stimuli were delivered at 561 nm. The responses of rods to stimulation were analyzed by using first-order kinetics. Results Two-photon excited fluorescence resulting from retinol production corresponded to the fraction of rhodopsin bleached. The photosensitivity of rhodopsin was estimated to be 6.88 ± 5.50 log scotopic troland. The rate of retinol clearance depended on intensity of incremental stimulation. Clearance was faster for stronger stimuli and time constants ranged from 50 to 300 seconds. Conclusions This study demonstrates a method for rapidly measuring the rate of clearance of retinol in vivo. Moreover, TPEF generated due to retinol can be used as a measure of rhodopsin depletion, similar to densitometry. This enhances the utility of two-photon ophthalmoscopy as a technique for evaluating the visual cycle in the living eye.

[1]  K. Palczewski,et al.  Retinal degeneration in animal models with a defective visual cycle. , 2013, Drug discovery today. Disease models.

[2]  K. Palczewski,et al.  Key enzymes of the retinoid (visual) cycle in vertebrate retina. , 2012, Biochimica et biophysica acta.

[3]  K. Palczewski,et al.  Two-photon microscopy reveals early rod photoreceptor cell damage in light-exposed mutant mice , 2014, Proceedings of the National Academy of Sciences.

[4]  K. Palczewski,et al.  Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents. , 2007, Annual review of pharmacology and toxicology.

[5]  David R. Williams,et al.  Images of photoreceptors in living primate eyes using adaptive optics two-photon ophthalmoscopy , 2010, Biomedical optics express.

[6]  R. Weale,et al.  Rhodopsin Regeneration in Man , 1969, Nature.

[7]  Austin Roorda,et al.  Retinally stabilized cone-targeted stimulus delivery. , 2007, Optics express.

[8]  Krzysztof Palczewski,et al.  Noninvasive two-photon imaging reveals retinyl ester storage structures in the eye , 2004, The Journal of cell biology.

[9]  Y. Koutalos,et al.  Visual Cycle: Dependence of Retinol Production and Removal on Photoproduct Decay and Cell Morphology , 2006, The Journal of general physiology.

[10]  D R Williams,et al.  Supernormal vision and high-resolution retinal imaging through adaptive optics. , 1997, Journal of the Optical Society of America. A, Optics, image science, and vision.

[11]  B. Wiggert,et al.  Interphotoreceptor retinoid-binding protein (IRBP) promotes the release of all-trans retinol from the isolated retina following rhodopsin bleaching illumination. , 2005, Experimental eye research.

[12]  G. Chader,et al.  Interphotoreceptor retinoid-binding protein: role in delivery of retinol to the pigment epithelium. , 1989, Experimental eye research.

[13]  S. Spencer,et al.  Effect of light on endogenous ligands carried by interphotoreceptor retinoid-binding protein. , 1991, Experimental eye research.

[14]  T. Hebert,et al.  Adaptive optics scanning laser ophthalmoscopy. , 2002, Optics express.

[15]  P. Gouras,et al.  Impaired retinal function and vitamin A availability in mice lacking retinol‐binding protein , 1999, The EMBO journal.

[16]  R. Weale,et al.  Flash bleaching of rhodopsin in the human retina , 1969, The Journal of physiology.

[17]  O. Strauß Transport mechanisms of the retinal pigment epithelium to maintain of visual function , 2014 .

[18]  David R Williams,et al.  Endogenous fluorophores enable two-photon imaging of the primate eye. , 2014, Investigative ophthalmology & visual science.

[19]  G. Wald CAROTENOIDS AND THE VISUAL CYCLE , 1935, The Journal of general physiology.

[20]  M Alpern,et al.  Rhodopsin kinetics in the human eye , 1971, The Journal of physiology.

[21]  G. Fex,et al.  Retinol transfer across and between phospholipid bilayer membranes. , 1988, Biochimica et biophysica acta.

[22]  L. Cosmides From : The Cognitive Neurosciences , 1995 .

[23]  D. Dacey,et al.  Origins of perception : retinal ganglion cell diversity and the creation of parallel visual pathways , 2011 .

[24]  David R. Williams,et al.  Noninvasive multi–photon fluorescence microscopy resolves retinol and retinal–condensation products in mouse eyes , 2010, Nature Medicine.

[25]  H. Ripps,et al.  The rhodopsin cycle is preserved in IRBP “knockout” mice despite abnormalities in retinal structure and function , 2000, Visual Neuroscience.

[26]  A. Adler,et al.  Human interphotoreceptor matrix contains serum albumin and retinol-binding protein. , 2000, Experimental eye research.

[27]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[28]  A. Roorda,et al.  Intrinsic signals from human cone photoreceptors. , 2008, Investigative ophthalmology & visual science.

[29]  M. Cascella,et al.  Human infrared vision is triggered by two-photon chromophore isomerization , 2014, Proceedings of the National Academy of Sciences.

[30]  T. Lamb,et al.  Dark adaptation and the retinoid cycle of vision , 2004, Progress in Retinal and Eye Research.

[31]  G. Chader,et al.  INTERPHOTORECEPTOR RETINOID‐BINDING PROTEIN AND α‐TOCOPHEROL PRESERVE THE ISOMERIC AND OXIDATION STATE OF RETINOL , 1992, Photochemistry and photobiology.

[32]  W A RUSHTON,et al.  Measurement of the scotopic pigment in the living human eye , 1955, The Journal of physiology.

[33]  J. B. Massey,et al.  Mechanism of vitamin A movement between rod outer segments, interphotoreceptor retinoid-binding protein, and liposomes. , 1989, The Journal of biological chemistry.

[34]  Jennifer J. Hunter,et al.  Two-Photon Autofluorescence Imaging Reveals Cellular Structures Throughout the Retina of the Living Primate Eye , 2016, Investigative ophthalmology & visual science.

[35]  G. Chader,et al.  Interphotoreceptor retinoid-binding protein (IRBP). Molecular biology and physiological role in the visual cycle of rhodopsin. , 1993, Molecular neurobiology.

[36]  J. Dowling,et al.  Chemistry of Visual Adaptation in the Rat , 1960, Nature.

[37]  S. Wu,et al.  The retinoid cycle and retina disease , 2003, Vision Research.

[38]  Yiannis Koutalos,et al.  Reduction of all-trans retinal to all-trans retinol in the outer segments of frog and mouse rod photoreceptors. , 2005, Biophysical journal.

[39]  E. Pugh,et al.  Scanning laser ophthalmoscope measurement of local fundus reflectance and autofluorescence changes arising from rhodopsin bleaching and regeneration. , 2013, Investigative ophthalmology & visual science.

[40]  Alfredo Dubra,et al.  Registration of 2D Images from Fast Scanning Ophthalmic Instruments , 2010, WBIR.

[41]  C. Baumann,et al.  Kinetics of rhodopsin bleaching in the isolated human retina , 1973, Pflugers Archiv : European journal of physiology.

[42]  David Williams,et al.  Imaging Light Responses of Foveal Ganglion Cells in the Living Macaque Eye , 2014, The Journal of Neuroscience.

[43]  T. Lamb,et al.  Recovery of the human photopic electroretinogram after bleaching exposures: estimation of pigment regeneration kinetics , 2004, The Journal of physiology.

[44]  James T. Dobbins Image Quality Metrics for Digital Systems , 2000 .

[45]  Jennifer J. Hunter,et al.  New wrinkles in retinal densitometry. , 2014, Investigative ophthalmology & visual science.

[46]  K. Palczewski,et al.  Kinetics of visual pigment regeneration in excised mouse eyes and in mice with a targeted disruption of the gene encoding interphotoreceptor retinoid-binding protein or arrestin. , 1999, Biochemistry.

[47]  Y. Koutalos,et al.  Interphotoreceptor retinoid-binding protein is the physiologically relevant carrier that removes retinol from rod photoreceptor outer segments. , 2007, Biochemistry.

[48]  K. Palczewski,et al.  Chemistry of the Retinoid (Visual) Cycle , 2013, Chemical reviews.

[49]  H. Ripps The rhodopsin cycle: a twist in the tale. , 2001, Progress in brain research.

[50]  K. Palczewski,et al.  Confronting Complexity: the Interlink of Phototransduction and Retinoid Metabolism in the Vertebrate Retina , 2001, Progress in Retinal and Eye Research.

[51]  Y. Koutalos,et al.  Formation of all-trans retinol after visual pigment bleaching in mouse photoreceptors. , 2009, Investigative ophthalmology & visual science.

[52]  K. Palczewski,et al.  Rod outer segment retinol dehydrogenase: substrate specificity and role in phototransduction. , 1994, Biochemistry.

[53]  Krzysztof Palczewski,et al.  Noninvasive two-photon microscopy imaging of mouse retina and retinal pigment epithelium through the pupil of the eye , 2014, Nature Medicine.

[54]  W A RUSHTON,et al.  The difference spectrum and the photosensitivity of rhodopsin in the living human eye , 1956, The Journal of physiology.

[55]  David R. Williams,et al.  In Vivo Two-Photon Fluorescence Kinetics of Primate Rods and Cones , 2016, Investigative ophthalmology & visual science.