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Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity

Astrocytes play a crucial role in regulating sleep–wake behavior, and adenosine signaling is generally thought to be involved. Here we show multiple lines of evidence supporting that modulation of the sleep–wake behavior by astrocyte Ca(2+) activity could occur without adenosine signaling. In the ba...

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Autores principales: Peng, Wanling, Liu, Xiaotong, Ma, Guofen, Wu, Zhaofa, Wang, Ziyue, Fei, Xiang, Qin, Meiling, Wang, Lizhao, Li, Yulong, Zhang, Siyu, Xu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902472/
https://www.ncbi.nlm.nih.gov/pubmed/36746933
http://dx.doi.org/10.1038/s41421-022-00498-9
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author Peng, Wanling
Liu, Xiaotong
Ma, Guofen
Wu, Zhaofa
Wang, Ziyue
Fei, Xiang
Qin, Meiling
Wang, Lizhao
Li, Yulong
Zhang, Siyu
Xu, Min
author_facet Peng, Wanling
Liu, Xiaotong
Ma, Guofen
Wu, Zhaofa
Wang, Ziyue
Fei, Xiang
Qin, Meiling
Wang, Lizhao
Li, Yulong
Zhang, Siyu
Xu, Min
author_sort Peng, Wanling
collection PubMed
description Astrocytes play a crucial role in regulating sleep–wake behavior, and adenosine signaling is generally thought to be involved. Here we show multiple lines of evidence supporting that modulation of the sleep–wake behavior by astrocyte Ca(2+) activity could occur without adenosine signaling. In the basal forebrain and the brainstem, two brain regions that are known to be essential for sleep–wake regulation, chemogenetically-induced astrocyte Ca(2+) elevation significantly modulated the sleep–wake cycle. Although astrocyte Ca(2+) level positively correlated with the amount of extracellular adenosine, as revealed by a genetically encoded adenosine sensor, we found no detectable change in adenosine level after suppressing astrocyte Ca(2+) elevation, and transgenic mice lacking one of the major extracellular ATP-adenosine conversion enzymes showed similar extracellular adenosine level and astrocyte Ca(2+)-induced sleep modulation. Furthermore, astrocyte Ca(2+) is dependent primarily on local neuronal activity, causing brain region-specific regulation of the sleep–wake cycle. Thus, neural activity-dependent astrocyte activity could regulate the sleep–wake behavior independent of adenosine signaling.
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spelling pubmed-99024722023-02-08 Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity Peng, Wanling Liu, Xiaotong Ma, Guofen Wu, Zhaofa Wang, Ziyue Fei, Xiang Qin, Meiling Wang, Lizhao Li, Yulong Zhang, Siyu Xu, Min Cell Discov Article Astrocytes play a crucial role in regulating sleep–wake behavior, and adenosine signaling is generally thought to be involved. Here we show multiple lines of evidence supporting that modulation of the sleep–wake behavior by astrocyte Ca(2+) activity could occur without adenosine signaling. In the basal forebrain and the brainstem, two brain regions that are known to be essential for sleep–wake regulation, chemogenetically-induced astrocyte Ca(2+) elevation significantly modulated the sleep–wake cycle. Although astrocyte Ca(2+) level positively correlated with the amount of extracellular adenosine, as revealed by a genetically encoded adenosine sensor, we found no detectable change in adenosine level after suppressing astrocyte Ca(2+) elevation, and transgenic mice lacking one of the major extracellular ATP-adenosine conversion enzymes showed similar extracellular adenosine level and astrocyte Ca(2+)-induced sleep modulation. Furthermore, astrocyte Ca(2+) is dependent primarily on local neuronal activity, causing brain region-specific regulation of the sleep–wake cycle. Thus, neural activity-dependent astrocyte activity could regulate the sleep–wake behavior independent of adenosine signaling. Springer Nature Singapore 2023-02-07 /pmc/articles/PMC9902472/ /pubmed/36746933 http://dx.doi.org/10.1038/s41421-022-00498-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Peng, Wanling
Liu, Xiaotong
Ma, Guofen
Wu, Zhaofa
Wang, Ziyue
Fei, Xiang
Qin, Meiling
Wang, Lizhao
Li, Yulong
Zhang, Siyu
Xu, Min
Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
title Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
title_full Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
title_fullStr Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
title_full_unstemmed Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
title_short Adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
title_sort adenosine-independent regulation of the sleep–wake cycle by astrocyte activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9902472/
https://www.ncbi.nlm.nih.gov/pubmed/36746933
http://dx.doi.org/10.1038/s41421-022-00498-9
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