Cargando…

Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells

Visual processing depends on specific computations implemented by complex neural circuits. Here, we present a circuit-inspired model of retinal ganglion cell computation, targeted to explain their temporal dynamics and adaptation to contrast. To localize the sources of such processing, we used recor...

Descripción completa

Detalles Bibliográficos
Autores principales: Cui, Yuwei, Wang, Yanbin V, Park, Silvia J H, Demb, Jonathan B, Butts, Daniel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108594/
https://www.ncbi.nlm.nih.gov/pubmed/27841746
http://dx.doi.org/10.7554/eLife.19460
_version_ 1782467381839265792
author Cui, Yuwei
Wang, Yanbin V
Park, Silvia J H
Demb, Jonathan B
Butts, Daniel A
author_facet Cui, Yuwei
Wang, Yanbin V
Park, Silvia J H
Demb, Jonathan B
Butts, Daniel A
author_sort Cui, Yuwei
collection PubMed
description Visual processing depends on specific computations implemented by complex neural circuits. Here, we present a circuit-inspired model of retinal ganglion cell computation, targeted to explain their temporal dynamics and adaptation to contrast. To localize the sources of such processing, we used recordings at the levels of synaptic input and spiking output in the in vitro mouse retina. We found that an ON-Alpha ganglion cell's excitatory synaptic inputs were described by a divisive interaction between excitation and delayed suppression, which explained nonlinear processing that was already present in ganglion cell inputs. Ganglion cell output was further shaped by spike generation mechanisms. The full model accurately predicted spike responses with unprecedented millisecond precision, and accurately described contrast adaptation of the spike train. These results demonstrate how circuit and cell-intrinsic mechanisms interact for ganglion cell function and, more generally, illustrate the power of circuit-inspired modeling of sensory processing. DOI: http://dx.doi.org/10.7554/eLife.19460.001
format Online
Article
Text
id pubmed-5108594
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-51085942016-11-16 Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells Cui, Yuwei Wang, Yanbin V Park, Silvia J H Demb, Jonathan B Butts, Daniel A eLife Neuroscience Visual processing depends on specific computations implemented by complex neural circuits. Here, we present a circuit-inspired model of retinal ganglion cell computation, targeted to explain their temporal dynamics and adaptation to contrast. To localize the sources of such processing, we used recordings at the levels of synaptic input and spiking output in the in vitro mouse retina. We found that an ON-Alpha ganglion cell's excitatory synaptic inputs were described by a divisive interaction between excitation and delayed suppression, which explained nonlinear processing that was already present in ganglion cell inputs. Ganglion cell output was further shaped by spike generation mechanisms. The full model accurately predicted spike responses with unprecedented millisecond precision, and accurately described contrast adaptation of the spike train. These results demonstrate how circuit and cell-intrinsic mechanisms interact for ganglion cell function and, more generally, illustrate the power of circuit-inspired modeling of sensory processing. DOI: http://dx.doi.org/10.7554/eLife.19460.001 eLife Sciences Publications, Ltd 2016-11-14 /pmc/articles/PMC5108594/ /pubmed/27841746 http://dx.doi.org/10.7554/eLife.19460 Text en © 2016, Cui et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Cui, Yuwei
Wang, Yanbin V
Park, Silvia J H
Demb, Jonathan B
Butts, Daniel A
Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
title Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
title_full Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
title_fullStr Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
title_full_unstemmed Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
title_short Divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
title_sort divisive suppression explains high-precision firing and contrast adaptation in retinal ganglion cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108594/
https://www.ncbi.nlm.nih.gov/pubmed/27841746
http://dx.doi.org/10.7554/eLife.19460
work_keys_str_mv AT cuiyuwei divisivesuppressionexplainshighprecisionfiringandcontrastadaptationinretinalganglioncells
AT wangyanbinv divisivesuppressionexplainshighprecisionfiringandcontrastadaptationinretinalganglioncells
AT parksilviajh divisivesuppressionexplainshighprecisionfiringandcontrastadaptationinretinalganglioncells
AT dembjonathanb divisivesuppressionexplainshighprecisionfiringandcontrastadaptationinretinalganglioncells
AT buttsdaniela divisivesuppressionexplainshighprecisionfiringandcontrastadaptationinretinalganglioncells