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Cone-Opponent Ganglion Cells in the Primate Fovea Tuned to Noncardinal Color Directions.

Authors :
Godat, Tyler
Kohout, Kendall
Parkins, Keith
Qiang Yang
McGregor, Juliette E.
Merigan, William H.
Williams, David R.
Patterson, Sara S.
Source :
Journal of Neuroscience. 5/1/2024, Vol. 44 Issue 18, p1-14. 14p.
Publication Year :
2024

Abstract

A long-standing question in vision science is how the three cone photoreceptor types—long (L), medium (M), and short (S) wavelength sensitive—combine to generate our perception of color. Hue perception can be described along two opponent axes: red–green and blue– yellow. Psychophysical measurements of color appearance indicate that the cone inputs to the red–green and blue–yellow opponent axes are M vs. L + S and L vs. M + S, respectively. However, the “cardinal directions of color space” revealed by psychophysical measurements of color detection thresholds following adaptation are L vs. M and S vs. L + M. These cardinal directions match the most common cone opponent retinal ganglion cells (RGCs) in the primate retina. Accordingly, the cone opponency necessary for color appearance is thought to be established in the cortex. While neurons with the appropriate M vs. L + S and L vs. M + S opponency have been reported in the retina and lateral geniculate nucleus, their existence continues to be debated. Resolving this long-standing debate is necessary because a complete account of the cone opponency in the retinal output is critical for understanding how downstream neural circuits process color. Here, we performed adaptive optics calcium imaging to noninvasively measure foveal RGC light responses in the living Macaca fascicularis eye. We confirm the presence of L vs. M + S and M vs. L + S neurons with noncardinal cone opponency and demonstrate that coneopponent signals in the retinal output are more diverse than classically thought. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02706474
Volume :
44
Issue :
18
Database :
Academic Search Index
Journal :
Journal of Neuroscience
Publication Type :
Academic Journal
Accession number :
177049449
Full Text :
https://doi.org/10.1523/JNEUROSCI.1738-23.2024