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Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex

Somatostatin-positive (SOM) interneurons are integral for shaping cortical processing and their dynamic recruitment is likely necessary for adaptation to sensory experience and contextual information. We found that excitatory synapses on SOMs in layer 2/3 (L2/3) of primary visual cortex (V1) of mice...

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Autores principales: Grier, Bryce D., Parkins, Samuel, Omar, Jarra, Lee, Hey-Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10630508/
https://www.ncbi.nlm.nih.gov/pubmed/37935668
http://dx.doi.org/10.1038/s41467-023-42968-y
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author Grier, Bryce D.
Parkins, Samuel
Omar, Jarra
Lee, Hey-Kyoung
author_facet Grier, Bryce D.
Parkins, Samuel
Omar, Jarra
Lee, Hey-Kyoung
author_sort Grier, Bryce D.
collection PubMed
description Somatostatin-positive (SOM) interneurons are integral for shaping cortical processing and their dynamic recruitment is likely necessary for adaptation to sensory experience and contextual information. We found that excitatory synapses on SOMs in layer 2/3 (L2/3) of primary visual cortex (V1) of mice can be categorized into fast (F)- and slow (S)-Types based on the kinetics of the AMPA receptor-mediated current. Each SOM contains both types of synapses in varying proportions. The majority of local pyramidal neurons (PCs) make unitary connections with SOMs using both types, followed by those utilizing only S-Type, and a minority with only F-Type. Sensory experience differentially regulates synapses on SOMs, such that local F-Type synapses change with visual deprivation and S-Type synapses undergo plasticity with crossmodal auditory deprivation. Our results demonstrate that the two types of excitatory synapses add richness to the SOM circuit recruitment and undergo selective plasticity enabling dynamic adaptation of the adult V1.
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spelling pubmed-106305082023-11-07 Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex Grier, Bryce D. Parkins, Samuel Omar, Jarra Lee, Hey-Kyoung Nat Commun Article Somatostatin-positive (SOM) interneurons are integral for shaping cortical processing and their dynamic recruitment is likely necessary for adaptation to sensory experience and contextual information. We found that excitatory synapses on SOMs in layer 2/3 (L2/3) of primary visual cortex (V1) of mice can be categorized into fast (F)- and slow (S)-Types based on the kinetics of the AMPA receptor-mediated current. Each SOM contains both types of synapses in varying proportions. The majority of local pyramidal neurons (PCs) make unitary connections with SOMs using both types, followed by those utilizing only S-Type, and a minority with only F-Type. Sensory experience differentially regulates synapses on SOMs, such that local F-Type synapses change with visual deprivation and S-Type synapses undergo plasticity with crossmodal auditory deprivation. Our results demonstrate that the two types of excitatory synapses add richness to the SOM circuit recruitment and undergo selective plasticity enabling dynamic adaptation of the adult V1. Nature Publishing Group UK 2023-11-07 /pmc/articles/PMC10630508/ /pubmed/37935668 http://dx.doi.org/10.1038/s41467-023-42968-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Grier, Bryce D.
Parkins, Samuel
Omar, Jarra
Lee, Hey-Kyoung
Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
title Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
title_full Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
title_fullStr Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
title_full_unstemmed Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
title_short Selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
title_sort selective plasticity of fast and slow excitatory synapses on somatostatin interneurons in adult visual cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10630508/
https://www.ncbi.nlm.nih.gov/pubmed/37935668
http://dx.doi.org/10.1038/s41467-023-42968-y
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