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Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity

The detection of visual motion is a fundamental function of the visual system. How motion speed and direction are computed together at the cellular level, however, remains largely unknown. Here, we suggest a circuit mechanism by which excitatory inputs to direction-selective ganglion cells in the mo...

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Detalles Bibliográficos
Autores principales: Matsumoto, Akihiro, Briggman, Kevin L., Yonehara, Keisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865067/
https://www.ncbi.nlm.nih.gov/pubmed/31564498
http://dx.doi.org/10.1016/j.cub.2019.08.048
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author Matsumoto, Akihiro
Briggman, Kevin L.
Yonehara, Keisuke
author_facet Matsumoto, Akihiro
Briggman, Kevin L.
Yonehara, Keisuke
author_sort Matsumoto, Akihiro
collection PubMed
description The detection of visual motion is a fundamental function of the visual system. How motion speed and direction are computed together at the cellular level, however, remains largely unknown. Here, we suggest a circuit mechanism by which excitatory inputs to direction-selective ganglion cells in the mouse retina become sensitive to the motion speed and direction of image motion. Electrophysiological, imaging, and connectomic analyses provide evidence that the dendrites of ON direction-selective cells receive spatially offset and asymmetrically filtered glutamatergic inputs along motion-preference axis from asymmetrically wired bipolar and amacrine cell types with distinct release dynamics. A computational model shows that, with this spatiotemporal structure, the input amplitude becomes sensitive to speed and direction by a preferred direction enhancement mechanism. Our results highlight the role of an excitatory mechanism in retinal motion computation by which feature selectivity emerges from non-selective inputs.
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spelling pubmed-68650672019-11-22 Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity Matsumoto, Akihiro Briggman, Kevin L. Yonehara, Keisuke Curr Biol Article The detection of visual motion is a fundamental function of the visual system. How motion speed and direction are computed together at the cellular level, however, remains largely unknown. Here, we suggest a circuit mechanism by which excitatory inputs to direction-selective ganglion cells in the mouse retina become sensitive to the motion speed and direction of image motion. Electrophysiological, imaging, and connectomic analyses provide evidence that the dendrites of ON direction-selective cells receive spatially offset and asymmetrically filtered glutamatergic inputs along motion-preference axis from asymmetrically wired bipolar and amacrine cell types with distinct release dynamics. A computational model shows that, with this spatiotemporal structure, the input amplitude becomes sensitive to speed and direction by a preferred direction enhancement mechanism. Our results highlight the role of an excitatory mechanism in retinal motion computation by which feature selectivity emerges from non-selective inputs. Cell Press 2019-10-07 /pmc/articles/PMC6865067/ /pubmed/31564498 http://dx.doi.org/10.1016/j.cub.2019.08.048 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Matsumoto, Akihiro
Briggman, Kevin L.
Yonehara, Keisuke
Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity
title Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity
title_full Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity
title_fullStr Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity
title_full_unstemmed Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity
title_short Spatiotemporally Asymmetric Excitation Supports Mammalian Retinal Motion Sensitivity
title_sort spatiotemporally asymmetric excitation supports mammalian retinal motion sensitivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865067/
https://www.ncbi.nlm.nih.gov/pubmed/31564498
http://dx.doi.org/10.1016/j.cub.2019.08.048
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