Cargando…

Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells

Motion is an important aspect of visual information. The directions of visual motion are encoded in the retina by direction-selective ganglion cells (DSGCs). ON-OFF DSGCs and ON DSGCs co-stratify with starburst amacrine cells (SACs) in the inner plexiform layer and depend on SACs for their direction...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Bo, Zhang, Yifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538761/
https://www.ncbi.nlm.nih.gov/pubmed/37721959
http://dx.doi.org/10.1371/journal.pbio.3002301
_version_ 1785113369918832640
author Wang, Bo
Zhang, Yifeng
author_facet Wang, Bo
Zhang, Yifeng
author_sort Wang, Bo
collection PubMed
description Motion is an important aspect of visual information. The directions of visual motion are encoded in the retina by direction-selective ganglion cells (DSGCs). ON-OFF DSGCs and ON DSGCs co-stratify with starburst amacrine cells (SACs) in the inner plexiform layer and depend on SACs for their direction selectivity. J-type retinal ganglion cells (J-RGCs), a type of OFF DSGCs in the mouse retina, on the other hand, do not co-stratify with SACs, and how direction selectivity in J-RGCs emerges has not been understood. Here, we report that both the excitatory and inhibitory synaptic inputs to J-RGCs are direction-selective (DS), with the inhibitory inputs playing a more important role for direction selectivity. The DS inhibitory inputs come from SACs, and the functional connections between J-RGCs and SACs are spatially asymmetric. Thus, J-RGCs and SACs form functionally important synaptic contacts even though their dendritic arbors show little overlap. These findings underscore the need to look beyond the neurons’ stratification patterns in retinal circuit studies. Our results also highlight the critical role of SACs for retinal direction selectivity.
format Online
Article
Text
id pubmed-10538761
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-105387612023-09-29 Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells Wang, Bo Zhang, Yifeng PLoS Biol Research Article Motion is an important aspect of visual information. The directions of visual motion are encoded in the retina by direction-selective ganglion cells (DSGCs). ON-OFF DSGCs and ON DSGCs co-stratify with starburst amacrine cells (SACs) in the inner plexiform layer and depend on SACs for their direction selectivity. J-type retinal ganglion cells (J-RGCs), a type of OFF DSGCs in the mouse retina, on the other hand, do not co-stratify with SACs, and how direction selectivity in J-RGCs emerges has not been understood. Here, we report that both the excitatory and inhibitory synaptic inputs to J-RGCs are direction-selective (DS), with the inhibitory inputs playing a more important role for direction selectivity. The DS inhibitory inputs come from SACs, and the functional connections between J-RGCs and SACs are spatially asymmetric. Thus, J-RGCs and SACs form functionally important synaptic contacts even though their dendritic arbors show little overlap. These findings underscore the need to look beyond the neurons’ stratification patterns in retinal circuit studies. Our results also highlight the critical role of SACs for retinal direction selectivity. Public Library of Science 2023-09-18 /pmc/articles/PMC10538761/ /pubmed/37721959 http://dx.doi.org/10.1371/journal.pbio.3002301 Text en © 2023 Wang, Zhang https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Bo
Zhang, Yifeng
Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells
title Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells
title_full Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells
title_fullStr Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells
title_full_unstemmed Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells
title_short Asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of J-type retinal ganglion cells
title_sort asymmetric connections with starburst amacrine cells underlie the upward motion selectivity of j-type retinal ganglion cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538761/
https://www.ncbi.nlm.nih.gov/pubmed/37721959
http://dx.doi.org/10.1371/journal.pbio.3002301
work_keys_str_mv AT wangbo asymmetricconnectionswithstarburstamacrinecellsunderlietheupwardmotionselectivityofjtyperetinalganglioncells
AT zhangyifeng asymmetricconnectionswithstarburstamacrinecellsunderlietheupwardmotionselectivityofjtyperetinalganglioncells