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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10630508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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