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Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling

Astroglial networks mediated by gap junction channels contribute to neurotransmission and promote neuronal coordination. Connexin 30, one of the two main astroglial gap junction forming protein, alters at the behavioral level the reactivity of mice to novel environment and at the synaptic level exci...

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Autores principales: Pannasch, Ulrike, Dossi, Elena, Ezan, Pascal, Rouach, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519011/
https://www.ncbi.nlm.nih.gov/pubmed/30794327
http://dx.doi.org/10.1002/glia.23591
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author Pannasch, Ulrike
Dossi, Elena
Ezan, Pascal
Rouach, Nathalie
author_facet Pannasch, Ulrike
Dossi, Elena
Ezan, Pascal
Rouach, Nathalie
author_sort Pannasch, Ulrike
collection PubMed
description Astroglial networks mediated by gap junction channels contribute to neurotransmission and promote neuronal coordination. Connexin 30, one of the two main astroglial gap junction forming protein, alters at the behavioral level the reactivity of mice to novel environment and at the synaptic level excitatory transmission. However, the role and function of Cx30 at the neuronal network level remain unclear. We thus investigated whether Cx30 regulates neuronal population bursts and associated convulsive behavior. We found in vivo that Cx30 is upregulated by kainate‐induced seizures and that it regulates in turn the severity of associated behavioral seizures. Using electrophysiology ex vivo, we report that Cx30 regulates aberrant network activity via control of astroglial glutamate clearance independently of gap‐junction mediated biochemical coupling. Altogether, our results indicate that astroglial Cx30 is an important player in orchestrating neuronal network activity.
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spelling pubmed-65190112019-05-21 Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling Pannasch, Ulrike Dossi, Elena Ezan, Pascal Rouach, Nathalie Glia Research Articles Astroglial networks mediated by gap junction channels contribute to neurotransmission and promote neuronal coordination. Connexin 30, one of the two main astroglial gap junction forming protein, alters at the behavioral level the reactivity of mice to novel environment and at the synaptic level excitatory transmission. However, the role and function of Cx30 at the neuronal network level remain unclear. We thus investigated whether Cx30 regulates neuronal population bursts and associated convulsive behavior. We found in vivo that Cx30 is upregulated by kainate‐induced seizures and that it regulates in turn the severity of associated behavioral seizures. Using electrophysiology ex vivo, we report that Cx30 regulates aberrant network activity via control of astroglial glutamate clearance independently of gap‐junction mediated biochemical coupling. Altogether, our results indicate that astroglial Cx30 is an important player in orchestrating neuronal network activity. John Wiley & Sons, Inc. 2019-02-22 2019-06 /pmc/articles/PMC6519011/ /pubmed/30794327 http://dx.doi.org/10.1002/glia.23591 Text en © 2019 The Authors. Glia published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Pannasch, Ulrike
Dossi, Elena
Ezan, Pascal
Rouach, Nathalie
Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
title Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
title_full Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
title_fullStr Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
title_full_unstemmed Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
title_short Astroglial Cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
title_sort astroglial cx30 sustains neuronal population bursts independently of gap‐junction mediated biochemical coupling
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519011/
https://www.ncbi.nlm.nih.gov/pubmed/30794327
http://dx.doi.org/10.1002/glia.23591
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