Preserving inhibition with a disinhibitory microcircuit in the retina

Previously, we found that in the mammalian retina, inhibitory inputs onto starburst amacrine cells (SACs) are required for robust direction selectivity of On-Off direction-selective ganglion cells (On-Off DSGCs) against noisy backgrounds (Chen et al., 2016). However, the source of the inhibitory inp...

Full description

Bibliographic Details
Main Authors: Qiang Chen, Robert G Smith, Xiaolin Huang, Wei Wei
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-12-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/62618
_version_ 1818019333955125248
author Qiang Chen
Robert G Smith
Xiaolin Huang
Wei Wei
author_facet Qiang Chen
Robert G Smith
Xiaolin Huang
Wei Wei
author_sort Qiang Chen
collection DOAJ
description Previously, we found that in the mammalian retina, inhibitory inputs onto starburst amacrine cells (SACs) are required for robust direction selectivity of On-Off direction-selective ganglion cells (On-Off DSGCs) against noisy backgrounds (Chen et al., 2016). However, the source of the inhibitory inputs to SACs and how this inhibition confers noise resilience of DSGCs are unknown. Here, we show that when visual noise is present in the background, the motion-evoked inhibition to an On-Off DSGC is preserved by a disinhibitory motif consisting of a serially connected network of neighboring SACs presynaptic to the DSGC. This preservation of inhibition by a disinhibitory motif arises from the interaction between visually evoked network dynamics and short-term synaptic plasticity at the SAC-DSGC synapse. Although the disinhibitory microcircuit is well studied for its disinhibitory function in brain circuits, our results highlight the algorithmic flexibility of this motif beyond disinhibition due to the mutual influence between network and synaptic plasticity mechanisms.
first_indexed 2024-04-14T07:50:55Z
format Article
id doaj.art-81fb7e766fa9491694fa1cd96e3edbf2
institution Directory Open Access Journal
issn 2050-084X
language English
last_indexed 2024-04-14T07:50:55Z
publishDate 2020-12-01
publisher eLife Sciences Publications Ltd
record_format Article
series eLife
spelling doaj.art-81fb7e766fa9491694fa1cd96e3edbf22022-12-22T02:05:11ZengeLife Sciences Publications LtdeLife2050-084X2020-12-01910.7554/eLife.62618Preserving inhibition with a disinhibitory microcircuit in the retinaQiang Chen0Robert G Smith1https://orcid.org/0000-0001-5703-1324Xiaolin Huang2https://orcid.org/0000-0001-7367-8347Wei Wei3https://orcid.org/0000-0002-7771-5974Committee on Computational Neuroscience, University of Chicago, Chicago, United StatesDepartment of Neuroscience, University of Pennsylvania, Philadelphia, United StatesCommittee on Neurobiology, University of Chicago, Chicago, United StatesCommittee on Computational Neuroscience, University of Chicago, Chicago, United States; Committee on Neurobiology, University of Chicago, Chicago, United States; Department of Neurobiology, the University of Chicago, Chicago, United States; Grossman Institute for Neuroscience, Quantitative Biology and Human Behavior, University of Chicago, Chicago, United StatesPreviously, we found that in the mammalian retina, inhibitory inputs onto starburst amacrine cells (SACs) are required for robust direction selectivity of On-Off direction-selective ganglion cells (On-Off DSGCs) against noisy backgrounds (Chen et al., 2016). However, the source of the inhibitory inputs to SACs and how this inhibition confers noise resilience of DSGCs are unknown. Here, we show that when visual noise is present in the background, the motion-evoked inhibition to an On-Off DSGC is preserved by a disinhibitory motif consisting of a serially connected network of neighboring SACs presynaptic to the DSGC. This preservation of inhibition by a disinhibitory motif arises from the interaction between visually evoked network dynamics and short-term synaptic plasticity at the SAC-DSGC synapse. Although the disinhibitory microcircuit is well studied for its disinhibitory function in brain circuits, our results highlight the algorithmic flexibility of this motif beyond disinhibition due to the mutual influence between network and synaptic plasticity mechanisms.https://elifesciences.org/articles/62618retinadisinhibitiondirection selectivityshort-term synaptic plasticitycenter surround receptive fieldvisual motion
spellingShingle Qiang Chen
Robert G Smith
Xiaolin Huang
Wei Wei
Preserving inhibition with a disinhibitory microcircuit in the retina
eLife
retina
disinhibition
direction selectivity
short-term synaptic plasticity
center surround receptive field
visual motion
title Preserving inhibition with a disinhibitory microcircuit in the retina
title_full Preserving inhibition with a disinhibitory microcircuit in the retina
title_fullStr Preserving inhibition with a disinhibitory microcircuit in the retina
title_full_unstemmed Preserving inhibition with a disinhibitory microcircuit in the retina
title_short Preserving inhibition with a disinhibitory microcircuit in the retina
title_sort preserving inhibition with a disinhibitory microcircuit in the retina
topic retina
disinhibition
direction selectivity
short-term synaptic plasticity
center surround receptive field
visual motion
url https://elifesciences.org/articles/62618
work_keys_str_mv AT qiangchen preservinginhibitionwithadisinhibitorymicrocircuitintheretina
AT robertgsmith preservinginhibitionwithadisinhibitorymicrocircuitintheretina
AT xiaolinhuang preservinginhibitionwithadisinhibitorymicrocircuitintheretina
AT weiwei preservinginhibitionwithadisinhibitorymicrocircuitintheretina