High-sensitivity rod photoreceptor input to the blue-yellow color opponent pathway in macaque retina.
Abstract
Small bistratified cells (SBCs) in the primate retina carry a major blue-yellow opponent
signal to the brain. We found that SBCs also carry signals from rod photoreceptors,
with the same sign as S cone input. SBCs exhibited robust responses under low scotopic
conditions. Physiological and anatomical experiments indicated that this rod input
arose from the AII amacrine cell-mediated rod pathway. Rod and cone signals were both
present in SBCs at mesopic light levels. These findings have three implications. First,
more retinal circuits may multiplex rod and cone signals than were previously thought
to, efficiently exploiting the limited number of optic nerve fibers. Second, signals
from AII amacrine cells may diverge to most or all of the approximately 20 retinal
ganglion cell types in the peripheral primate retina. Third, rod input to SBCs may
be the substrate for behavioral biases toward perception of blue at mesopic light
levels.
Type
Journal articleSubject
Action PotentialsAmacrine Cells
Aminobutyrates
Animals
Color
Excitatory Amino Acid Agonists
Gap Junctions
In Vitro Techniques
Light
Macaca fascicularis
Macaca mulatta
Microelectrodes
Photic Stimulation
Retina
Retinal Bipolar Cells
Retinal Cone Photoreceptor Cells
Retinal Ganglion Cells
Retinal Rod Photoreceptor Cells
Time Factors
Vision, Ocular
Visual Pathways
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https://hdl.handle.net/10161/9724Published Version (Please cite this version)
10.1038/nn.2353Publication Info
Field, Greg D; Greschner, Martin; Gauthier, Jeffrey L; Rangel, Carolina; Shlens, Jonathon;
Sher, Alexander; ... Chichilnisky, EJ (2009). High-sensitivity rod photoreceptor input to the blue-yellow color opponent pathway
in macaque retina. Nat Neurosci, 12(9). pp. 1159-1164. 10.1038/nn.2353. Retrieved from https://hdl.handle.net/10161/9724.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Greg D. Field
Adjunct Associate Professor of Neurobiology
My laboratory studies how the retina processes visual scenes and transmits this information
to the brain. We use multi-electrode arrays to record the activity of hundreds of
retina neurons simultaneously in conjunction with transgenic mouse lines and chemogenetics
to manipulate neural circuit function. We are interested in three major areas. First,
we work to understand how neurons in the retina are functionally connected. Second
we are studying how light-adaptation and circadian rhythms a

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