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Astrocytic chloride is brain state dependent and modulates inhibitory neurotransmission in mice

Information transfer within neuronal circuits depends on the balance and recurrent activity of excitatory and inhibitory neurotransmission. Chloride (Cl(−)) is the major central nervous system (CNS) anion mediating inhibitory neurotransmission. Astrocytes are key homoeostatic glial cells populating...

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Detalles Bibliográficos
Autores principales: Untiet, Verena, Beinlich, Felix R. M., Kusk, Peter, Kang, Ning, Ladrón-de-Guevara, Antonio, Song, Wei, Kjaerby, Celia, Andersen, Mie, Hauglund, Natalie, Bojarowska, Zuzanna, Sigurdsson, Björn, Deng, Saiyue, Hirase, Hajime, Petersen, Nicolas C., Verkhratsky, Alexei, Nedergaard, Maiken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073105/
https://www.ncbi.nlm.nih.gov/pubmed/37015909
http://dx.doi.org/10.1038/s41467-023-37433-9
Descripción
Sumario:Information transfer within neuronal circuits depends on the balance and recurrent activity of excitatory and inhibitory neurotransmission. Chloride (Cl(−)) is the major central nervous system (CNS) anion mediating inhibitory neurotransmission. Astrocytes are key homoeostatic glial cells populating the CNS, although the role of these cells in regulating excitatory-inhibitory balance remains unexplored. Here we show that astrocytes act as a dynamic Cl(−) reservoir regulating Cl(−) homoeostasis in the CNS. We found that intracellular chloride concentration ([Cl(−)](i)) in astrocytes is high and stable during sleep. In awake mice astrocytic [Cl(−)](i) is lower and exhibits large fluctuation in response to both sensory input and motor activity. Optogenetic manipulation of astrocytic [Cl(−)](i) directly modulates neuronal activity during locomotion or whisker stimulation. Astrocytes thus serve as a dynamic source of extracellular Cl(−) available for GABAergic transmission in awake mice, which represents a mechanism for modulation of the inhibitory tone during sustained neuronal activity.