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Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons
Perisomatic inhibition of pyramidal neurons (PNs) coordinates cortical network activity during sensory processing, and this role is mainly attributed to parvalbumin-expressing basket cells (BCs). However, cannabinoid receptor type 1 (CB1)-expressing interneurons are also BCs, but the connectivity an...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433882/ https://www.ncbi.nlm.nih.gov/pubmed/36001978 http://dx.doi.org/10.1016/j.celrep.2022.111202 |
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author | Koukouli, Fani Montmerle, Martin Aguirre, Andrea De Brito Van Velze, Marcel Peixoto, Jérémy Choudhary, Vikash Varilh, Marjorie Julio-Kalajzic, Francisca Allene, Camille Mendéz, Pablo Zerlaut, Yann Marsicano, Giovanni Schlüter, Oliver M. Rebola, Nelson Bacci, Alberto Lourenço, Joana |
author_facet | Koukouli, Fani Montmerle, Martin Aguirre, Andrea De Brito Van Velze, Marcel Peixoto, Jérémy Choudhary, Vikash Varilh, Marjorie Julio-Kalajzic, Francisca Allene, Camille Mendéz, Pablo Zerlaut, Yann Marsicano, Giovanni Schlüter, Oliver M. Rebola, Nelson Bacci, Alberto Lourenço, Joana |
author_sort | Koukouli, Fani |
collection | PubMed |
description | Perisomatic inhibition of pyramidal neurons (PNs) coordinates cortical network activity during sensory processing, and this role is mainly attributed to parvalbumin-expressing basket cells (BCs). However, cannabinoid receptor type 1 (CB1)-expressing interneurons are also BCs, but the connectivity and function of these elusive but prominent neocortical inhibitory neurons are unclear. We find that their connectivity pattern is visual area specific. Persistently active CB1 signaling suppresses GABA release from CB1 BCs in the medial secondary visual cortex (V2M), but not in the primary visual cortex (V1). Accordingly, in vivo, tonic CB1 signaling is responsible for higher but less coordinated PN activity in the V2M than in the V1. These differential firing dynamics in the V1 and V2M can be captured by a computational network model that incorporates visual-area-specific properties. Our results indicate a differential CB1-mediated mechanism controlling PN activity, suggesting an alternative connectivity scheme of a specific GABAergic circuit in different cortical areas. |
format | Online Article Text |
id | pubmed-9433882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94338822022-09-08 Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons Koukouli, Fani Montmerle, Martin Aguirre, Andrea De Brito Van Velze, Marcel Peixoto, Jérémy Choudhary, Vikash Varilh, Marjorie Julio-Kalajzic, Francisca Allene, Camille Mendéz, Pablo Zerlaut, Yann Marsicano, Giovanni Schlüter, Oliver M. Rebola, Nelson Bacci, Alberto Lourenço, Joana Cell Rep Article Perisomatic inhibition of pyramidal neurons (PNs) coordinates cortical network activity during sensory processing, and this role is mainly attributed to parvalbumin-expressing basket cells (BCs). However, cannabinoid receptor type 1 (CB1)-expressing interneurons are also BCs, but the connectivity and function of these elusive but prominent neocortical inhibitory neurons are unclear. We find that their connectivity pattern is visual area specific. Persistently active CB1 signaling suppresses GABA release from CB1 BCs in the medial secondary visual cortex (V2M), but not in the primary visual cortex (V1). Accordingly, in vivo, tonic CB1 signaling is responsible for higher but less coordinated PN activity in the V2M than in the V1. These differential firing dynamics in the V1 and V2M can be captured by a computational network model that incorporates visual-area-specific properties. Our results indicate a differential CB1-mediated mechanism controlling PN activity, suggesting an alternative connectivity scheme of a specific GABAergic circuit in different cortical areas. Cell Press 2022-08-23 /pmc/articles/PMC9433882/ /pubmed/36001978 http://dx.doi.org/10.1016/j.celrep.2022.111202 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Koukouli, Fani Montmerle, Martin Aguirre, Andrea De Brito Van Velze, Marcel Peixoto, Jérémy Choudhary, Vikash Varilh, Marjorie Julio-Kalajzic, Francisca Allene, Camille Mendéz, Pablo Zerlaut, Yann Marsicano, Giovanni Schlüter, Oliver M. Rebola, Nelson Bacci, Alberto Lourenço, Joana Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
title | Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
title_full | Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
title_fullStr | Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
title_full_unstemmed | Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
title_short | Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
title_sort | visual-area-specific tonic modulation of gaba release by endocannabinoids sets the activity and coordination of neocortical principal neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433882/ https://www.ncbi.nlm.nih.gov/pubmed/36001978 http://dx.doi.org/10.1016/j.celrep.2022.111202 |
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