Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783472022083338240 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6865067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT matsumotoakihiro spatiotemporallyasymmetricexcitationsupportsmammalianretinalmotionsensitivity AT briggmankevinl spatiotemporallyasymmetricexcitationsupportsmammalianretinalmotionsensitivity AT yoneharakeisuke spatiotemporallyasymmetricexcitationsupportsmammalianretinalmotionsensitivity |