Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783418567954268160 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6519011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pannaschulrike astroglialcx30sustainsneuronalpopulationburstsindependentlyofgapjunctionmediatedbiochemicalcoupling AT dossielena astroglialcx30sustainsneuronalpopulationburstsindependentlyofgapjunctionmediatedbiochemicalcoupling AT ezanpascal astroglialcx30sustainsneuronalpopulationburstsindependentlyofgapjunctionmediatedbiochemicalcoupling AT rouachnathalie astroglialcx30sustainsneuronalpopulationburstsindependentlyofgapjunctionmediatedbiochemicalcoupling |