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Circuitry for color coding in the primate retina.
Abstract
Human color vision starts with the signals from three cone photoreceptor types, maximally sensitive to long (L-cone), middle (M-cone), and short (S-cone) wavelengths. Within the retina these signals combine in an antagonistic way to form red-green and blue-yellow spectral opponent pathways. In the classical model this antagonism is thought to arise from the convergence of cone type-specific excitatory and inhibitory inputs to retinal ganglion cells. The circuitry for spectral opponency is now being investigated using an in vitro preparation of the macaque monkey retina. Intracellular recording and staining has shown that blue-ON/yellow-OFF opponent responses arise from a distinctive bistratified ganglion cell type. Surprisingly, this cone opponency appears to arise by dual excitatory cone bipolar cell inputs: an ON bipolar cell that contacts only S-cones and an OFF bipolar cell that contacts L- and M-cones. Red-green spectral opponency has long been linked to the midget ganglion cells, but an underlying mechanism remains unclear. For example, receptive field mapping argues for segregation of L-and M-cone signals to the midget cell center and surround, but horizontal cell interneurons, believed to generate the inhibitory surround, lack opponency and cannot contribute selective L- or M-cone input to the midget cell surround. The solution to this color puzzle no doubt lies in the great diversity of cell types in the primate retina that still await discovery and analysis.
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“Molecular genetics, physiology and anatomy have converged to indicate that in primates, there is a single bipolar cell type that is highly S cone specific and there are others that are highly L/M cone specific (Figure 5) (Dacey, 1996, Li & DeVries, 2006, Martin & Grunert, 1999).”
From The genetics of normal and defective color vision (2011) · cites this paper as Dacey, 1996
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- [3]Sterling, P. (1990) in The Synaptic Organization of the Brain, ed. Shepherd, G. M. (Oxford Univ. Press, New York), pp. 170–213.
- [4]Rodieck, R. W. (1988) in Comparative Primate Biology, ed. Steklis, H. D. (Liss, New York), Vol. 4, pp. 203–278.
- [13]Zrenner, E., Abramov, I., Akita, M., Cowey, A., Livingstone, M. & Valberg, A. (1990) in Visual Perception: The Neurophysiological Foundations, eds. Spillman, L. & Werner, J. S. (Academic, San Diego), pp. 163–204.
- [15]Tauchi, M. & Masland, R. H. (1984) Proc. R. Soc. London B 223, 101-119.
- [16]Vaney, D. I. (1985) Proc. R. Soc. London B 224, 475–488.
- [40]Wässle, H., Grünert, U., Martin, P. R. & Boycott, B. B. (1993) in Structural and Functional Organization of the Neocortex, Experimental Brain Research Series 24, eds. Albowitz, B., Albus, K., Kuhnt, U., Northdurft, H.-Ch. & Wahle, P. (Springer, New York), pp. 94–104.
- [45]Dacheux, R. F. & Raviola, E. (1990) Proc. R. Soc. London B 239, 213-230.
- [48]Dacey, D. M., Lee, B. B., Stafford, D. K., Pokorny, J. & Smith, V. C. (1995) Science, in press.
- [49]Lennie, P., Haake, P. W. & Williams, D. R. (1991) in Computational Models of Visual Processing, eds. Landy, M. S. & Movshon, J. A. (MIT Press, Cambridge, MA), pp. 71–82.
- [52]Rodieck, R. W. (1991) in From Pigments to Perception, eds. Valberg, A. & Lee, B. B. (Plenum, New York), pp. 83–93.
Cited by
Sorted by citations
Yücel, Y. (2003) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(03)00026-0 · Cited by 384
The genetics of normal and defective color vision
Neitz, J., & Neitz, M. (2011) · Vision Research · doi:10.1016/j.visres.2010.12.002 · Cited by 377
Metadata
- Authors
- Dacey, D. M.
- Affiliations
- Department of Biological Structure, University of Washington, Seattle 98195-7420, USA.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1996-01-23
- Volume
- 93
- Issue
- 2
- Pages
- 582-588
- ISSN
- 0027-8424
- 1091-6490
- Cited by
- 158
- References
- 0
- Language
- en
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