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Hippocampal hub neurons maintain distinct connectivity throughout their lifetime
The temporal embryonic origins of cortical GABA neurons are critical for their specialization. In the neonatal hippocampus, GABA cells born the earliest (ebGABAs) operate as ‘hubs’ by orchestrating population synchrony. However, their adult fate remains largely unknown. To fill this gap, we have exa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486410/ https://www.ncbi.nlm.nih.gov/pubmed/32917906 http://dx.doi.org/10.1038/s41467-020-18432-6 |
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author | Bocchio, Marco Gouny, Claire Angulo-Garcia, David Toulat, Tom Tressard, Thomas Quiroli, Eleonora Baude, Agnès Cossart, Rosa |
author_facet | Bocchio, Marco Gouny, Claire Angulo-Garcia, David Toulat, Tom Tressard, Thomas Quiroli, Eleonora Baude, Agnès Cossart, Rosa |
author_sort | Bocchio, Marco |
collection | PubMed |
description | The temporal embryonic origins of cortical GABA neurons are critical for their specialization. In the neonatal hippocampus, GABA cells born the earliest (ebGABAs) operate as ‘hubs’ by orchestrating population synchrony. However, their adult fate remains largely unknown. To fill this gap, we have examined CA1 ebGABAs using a combination of electrophysiology, neurochemical analysis, optogenetic connectivity mapping as well as ex vivo and in vivo calcium imaging. We show that CA1 ebGABAs not only operate as hubs during development, but also maintain distinct morpho-physiological and connectivity profiles, including a bias for long-range targets and local excitatory inputs. In vivo, ebGABAs are activated during locomotion, correlate with CA1 cell assemblies and display high functional connectivity. Hence, ebGABAs are specified from birth to ensure unique functions throughout their lifetime. In the adult brain, this may take the form of a long-range hub role through the coordination of cell assemblies across distant regions. |
format | Online Article Text |
id | pubmed-7486410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74864102020-09-25 Hippocampal hub neurons maintain distinct connectivity throughout their lifetime Bocchio, Marco Gouny, Claire Angulo-Garcia, David Toulat, Tom Tressard, Thomas Quiroli, Eleonora Baude, Agnès Cossart, Rosa Nat Commun Article The temporal embryonic origins of cortical GABA neurons are critical for their specialization. In the neonatal hippocampus, GABA cells born the earliest (ebGABAs) operate as ‘hubs’ by orchestrating population synchrony. However, their adult fate remains largely unknown. To fill this gap, we have examined CA1 ebGABAs using a combination of electrophysiology, neurochemical analysis, optogenetic connectivity mapping as well as ex vivo and in vivo calcium imaging. We show that CA1 ebGABAs not only operate as hubs during development, but also maintain distinct morpho-physiological and connectivity profiles, including a bias for long-range targets and local excitatory inputs. In vivo, ebGABAs are activated during locomotion, correlate with CA1 cell assemblies and display high functional connectivity. Hence, ebGABAs are specified from birth to ensure unique functions throughout their lifetime. In the adult brain, this may take the form of a long-range hub role through the coordination of cell assemblies across distant regions. Nature Publishing Group UK 2020-09-11 /pmc/articles/PMC7486410/ /pubmed/32917906 http://dx.doi.org/10.1038/s41467-020-18432-6 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bocchio, Marco Gouny, Claire Angulo-Garcia, David Toulat, Tom Tressard, Thomas Quiroli, Eleonora Baude, Agnès Cossart, Rosa Hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
title | Hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
title_full | Hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
title_fullStr | Hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
title_full_unstemmed | Hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
title_short | Hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
title_sort | hippocampal hub neurons maintain distinct connectivity throughout their lifetime |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486410/ https://www.ncbi.nlm.nih.gov/pubmed/32917906 http://dx.doi.org/10.1038/s41467-020-18432-6 |
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