Mapping nonlinear receptive field structure in primate retina at single cone resolution.
Abstract
The function of a neural circuit is shaped by the computations performed by its interneurons,
which in many cases are not easily accessible to experimental investigation. Here,
we elucidate the transformation of visual signals flowing from the input to the output
of the primate retina, using a combination of large-scale multi-electrode recordings
from an identified ganglion cell type, visual stimulation targeted at individual cone
photoreceptors, and a hierarchical computational model. The results reveal nonlinear
subunits in the circuity of OFF midget ganglion cells, which subserve high-resolution
vision. The model explains light responses to a variety of stimuli more accurately
than a linear model, including stimuli targeted to cones within and across subunits.
The recovered model components are consistent with known anatomical organization of
midget bipolar interneurons. These results reveal the spatial structure of linear
and nonlinear encoding, at the resolution of single cells and at the scale of complete
circuits.
Type
Journal articleSubject
NeuronsRetina
Animals
Macaca
Photic Stimulation
Models, Neurological
Computer Simulation
Retinal Cone Photoreceptor Cells
Neuroanatomical Tract-Tracing Techniques
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https://hdl.handle.net/10161/16628Published Version (Please cite this version)
10.7554/elife.05241Publication Info
Freeman, Jeremy; Field, Greg D; Li, Peter H; Greschner, Martin; Gunning, Deborah E;
Mathieson, Keith; ... Chichilnisky, EJ (2015). Mapping nonlinear receptive field structure in primate retina at single cone resolution.
eLife, 4(OCTOBER2015). 10.7554/elife.05241. Retrieved from https://hdl.handle.net/10161/16628.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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