Though it has been known that color vision is mediated by three types of photoreceptors for some 200 years, there is little information about the spacing and packing arrangement of the short (S), middle (M), and long (L) wavelength sensitive cones. The spatial organization of the S cones is the best known, while little is known about the relative numbers and distribution of M and L cones. During the last grant period we established the viability of a new technique, Photopigment Transmittance Imaging, to classify cones in the fresh, excised primate retina. Full color images of the photoreceptor mosaic are acquired with a high resolution, high sensitivity CCD camera at light levels that do not bleach substantial amounts of pigment. This allows cones to be typed on the basis of the absorption spectra of their photopigments. The goal of this proposal is to use our imaging technique to map the three interleaved cone submosaics across the monkey and human retina. Such maps may eventually help 1) to understand how trichromacy is incorporated into the retina with minimal cost for spatial vision, 2) to explore the contributions of the three cone types to the post-receptoral channels that are posited from psychophysical experiments, 3) to determine the neural circuitry underlying color vision, and 4) to study the mechanisms responsible for the development of the trichromatic cone mosaic. Our preparation for the classification of cones also allows us to measure the efficiency with which the photoreceptors collect the light incident on the retina. Such measurements will allow the first comprehensive analysis of the fate of photons as they pass through the photoreceptor layer.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY009625-04
Application #
2163303
Study Section
Visual Sciences C Study Section (VISC)
Project Start
1992-05-01
Project End
1998-04-30
Budget Start
1995-05-01
Budget End
1996-04-30
Support Year
4
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Rochester
Department
Miscellaneous
Type
Schools of Arts and Sciences
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
Liao, Hsi-Wen; Ren, Xiaozhi; Peterson, Beth B et al. (2016) Melanopsin-expressing ganglion cells on macaque and human retinas form two morphologically distinct populations. J Comp Neurol 524:2845-72
Dacey, Dennis M; Crook, Joanna D; Packer, Orin S (2014) Distinct synaptic mechanisms create parallel S-ON and S-OFF color opponent pathways in the primate retina. Vis Neurosci 31:139-51
Joo, Hannah R; Peterson, Beth B; Dacey, Dennis M et al. (2013) Recurrent axon collaterals of intrinsically photosensitive retinal ganglion cells. Vis Neurosci 30:175-82
Schmidt, Tiffany M; Do, Michael Tri H; Dacey, Dennis et al. (2011) Melanopsin-positive intrinsically photosensitive retinal ganglion cells: from form to function. J Neurosci 31:16094-101
Smith, Vivianne C; Pokorny, Joel; Lee, Barry B et al. (2008) Sequential processing in vision: The interaction of sensitivity regulation and temporal dynamics. Vision Res 48:2649-56
Gamlin, Paul D R; McDougal, David H; Pokorny, Joel et al. (2007) Human and macaque pupil responses driven by melanopsin-containing retinal ganglion cells. Vision Res 47:946-54
Packer, Orin S; Dacey, Dennis M (2005) Synergistic center-surround receptive field model of monkey H1 horizontal cells. J Vis 5:1038-54
McMahon, Matthew J; Packer, Orin S; Dacey, Dennis M (2004) The classical receptive field surround of primate parasol ganglion cells is mediated primarily by a non-GABAergic pathway. J Neurosci 24:3736-45
Diller, Lisa; Packer, Orin S; Verweij, Jan et al. (2004) L and M cone contributions to the midget and parasol ganglion cell receptive fields of macaque monkey retina. J Neurosci 24:1079-88
Dacey, Dennis M; Packer, Orin S (2003) Colour coding in the primate retina: diverse cell types and cone-specific circuitry. Curr Opin Neurobiol 13:421-7

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