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Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance

Astrocytes may function as mediators of the impact of noradrenaline on neuronal function. Activation of glial α1-adrenergic receptors triggers rapid astrocytic Ca(2+) elevation and facilitates synaptic plasticity, while activation of β-adrenergic receptors elevates cAMP levels and modulates memory c...

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Autores principales: Oe, Yuki, Wang, Xiaowen, Patriarchi, Tommaso, Konno, Ayumu, Ozawa, Katsuya, Yahagi, Kazuko, Hirai, Hirokazu, Tian, Lin, McHugh, Thomas J., Hirase, Hajime
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981284/
https://www.ncbi.nlm.nih.gov/pubmed/31980655
http://dx.doi.org/10.1038/s41467-020-14378-x
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author Oe, Yuki
Wang, Xiaowen
Patriarchi, Tommaso
Konno, Ayumu
Ozawa, Katsuya
Yahagi, Kazuko
Hirai, Hirokazu
Tian, Lin
McHugh, Thomas J.
Hirase, Hajime
author_facet Oe, Yuki
Wang, Xiaowen
Patriarchi, Tommaso
Konno, Ayumu
Ozawa, Katsuya
Yahagi, Kazuko
Hirai, Hirokazu
Tian, Lin
McHugh, Thomas J.
Hirase, Hajime
author_sort Oe, Yuki
collection PubMed
description Astrocytes may function as mediators of the impact of noradrenaline on neuronal function. Activation of glial α1-adrenergic receptors triggers rapid astrocytic Ca(2+) elevation and facilitates synaptic plasticity, while activation of β-adrenergic receptors elevates cAMP levels and modulates memory consolidation. However, the dynamics of these processes in behaving mice remain unexplored, as do the interactions between the distinct second messenger pathways. Here we simultaneously monitored astrocytic Ca(2+) and cAMP and demonstrate that astrocytic second messengers are regulated in a temporally distinct manner. In behaving mice, we found that while an abrupt facial air puff triggered transient increases in noradrenaline release and large cytosolic astrocytic Ca(2+) elevations, cAMP changes were not detectable. By contrast, repeated aversive stimuli that lead to prolonged periods of vigilance were accompanied by robust noradrenergic axonal activity and gradual sustained cAMP increases. Our findings suggest distinct astrocytic signaling pathways can integrate noradrenergic activity during vigilance states to mediate distinct functions supporting memory.
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spelling pubmed-69812842020-01-27 Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance Oe, Yuki Wang, Xiaowen Patriarchi, Tommaso Konno, Ayumu Ozawa, Katsuya Yahagi, Kazuko Hirai, Hirokazu Tian, Lin McHugh, Thomas J. Hirase, Hajime Nat Commun Article Astrocytes may function as mediators of the impact of noradrenaline on neuronal function. Activation of glial α1-adrenergic receptors triggers rapid astrocytic Ca(2+) elevation and facilitates synaptic plasticity, while activation of β-adrenergic receptors elevates cAMP levels and modulates memory consolidation. However, the dynamics of these processes in behaving mice remain unexplored, as do the interactions between the distinct second messenger pathways. Here we simultaneously monitored astrocytic Ca(2+) and cAMP and demonstrate that astrocytic second messengers are regulated in a temporally distinct manner. In behaving mice, we found that while an abrupt facial air puff triggered transient increases in noradrenaline release and large cytosolic astrocytic Ca(2+) elevations, cAMP changes were not detectable. By contrast, repeated aversive stimuli that lead to prolonged periods of vigilance were accompanied by robust noradrenergic axonal activity and gradual sustained cAMP increases. Our findings suggest distinct astrocytic signaling pathways can integrate noradrenergic activity during vigilance states to mediate distinct functions supporting memory. Nature Publishing Group UK 2020-01-24 /pmc/articles/PMC6981284/ /pubmed/31980655 http://dx.doi.org/10.1038/s41467-020-14378-x 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
Oe, Yuki
Wang, Xiaowen
Patriarchi, Tommaso
Konno, Ayumu
Ozawa, Katsuya
Yahagi, Kazuko
Hirai, Hirokazu
Tian, Lin
McHugh, Thomas J.
Hirase, Hajime
Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
title Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
title_full Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
title_fullStr Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
title_full_unstemmed Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
title_short Distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
title_sort distinct temporal integration of noradrenaline signaling by astrocytic second messengers during vigilance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981284/
https://www.ncbi.nlm.nih.gov/pubmed/31980655
http://dx.doi.org/10.1038/s41467-020-14378-x
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