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Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity

The dendrites of starburst amacrine cells (SACs) in the mammalian retina are preferentially activated by motion in the centrifugal direction, a property that is important for generating direction selectivity in direction selective ganglion cells (DSGCs). A candidate mechanism underlying the centrifu...

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Autores principales: Chen, Qiang, Pei, Zhe, Koren, David, Wei, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176353/
https://www.ncbi.nlm.nih.gov/pubmed/27929372
http://dx.doi.org/10.7554/eLife.21053
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author Chen, Qiang
Pei, Zhe
Koren, David
Wei, Wei
author_facet Chen, Qiang
Pei, Zhe
Koren, David
Wei, Wei
author_sort Chen, Qiang
collection PubMed
description The dendrites of starburst amacrine cells (SACs) in the mammalian retina are preferentially activated by motion in the centrifugal direction, a property that is important for generating direction selectivity in direction selective ganglion cells (DSGCs). A candidate mechanism underlying the centrifugal direction selectivity of SAC dendrites is synaptic inhibition onto SACs. Here we disrupted this inhibition by perturbing distinct sets of GABAergic inputs onto SACs – removing either GABA release or GABA receptors from SACs. We found that lateral inhibition onto Off SACs from non-SAC amacrine cells is required for optimal direction selectivity of the Off pathway. In contrast, lateral inhibition onto On SACs is not necessary for direction selectivity of the On pathway when the moving object is on a homogenous background, but is required when the background is noisy. These results demonstrate that distinct sets of inhibitory mechanisms are recruited to generate direction selectivity under different visual conditions. DOI: http://dx.doi.org/10.7554/eLife.21053.001
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spelling pubmed-51763532016-12-23 Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity Chen, Qiang Pei, Zhe Koren, David Wei, Wei eLife Neuroscience The dendrites of starburst amacrine cells (SACs) in the mammalian retina are preferentially activated by motion in the centrifugal direction, a property that is important for generating direction selectivity in direction selective ganglion cells (DSGCs). A candidate mechanism underlying the centrifugal direction selectivity of SAC dendrites is synaptic inhibition onto SACs. Here we disrupted this inhibition by perturbing distinct sets of GABAergic inputs onto SACs – removing either GABA release or GABA receptors from SACs. We found that lateral inhibition onto Off SACs from non-SAC amacrine cells is required for optimal direction selectivity of the Off pathway. In contrast, lateral inhibition onto On SACs is not necessary for direction selectivity of the On pathway when the moving object is on a homogenous background, but is required when the background is noisy. These results demonstrate that distinct sets of inhibitory mechanisms are recruited to generate direction selectivity under different visual conditions. DOI: http://dx.doi.org/10.7554/eLife.21053.001 eLife Sciences Publications, Ltd 2016-12-08 /pmc/articles/PMC5176353/ /pubmed/27929372 http://dx.doi.org/10.7554/eLife.21053 Text en © 2016, Chen 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
Chen, Qiang
Pei, Zhe
Koren, David
Wei, Wei
Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
title Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
title_full Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
title_fullStr Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
title_full_unstemmed Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
title_short Stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
title_sort stimulus-dependent recruitment of lateral inhibition underlies retinal direction selectivity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176353/
https://www.ncbi.nlm.nih.gov/pubmed/27929372
http://dx.doi.org/10.7554/eLife.21053
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AT peizhe stimulusdependentrecruitmentoflateralinhibitionunderliesretinaldirectionselectivity
AT korendavid stimulusdependentrecruitmentoflateralinhibitionunderliesretinaldirectionselectivity
AT weiwei stimulusdependentrecruitmentoflateralinhibitionunderliesretinaldirectionselectivity