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Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity

The plasticity of astrocytes is fundamental for their principal function, maintaining homeostasis of the central nervous system throughout life, and is associated with diverse exposomal challenges. Here, we used cultured astrocytes to investigate at subcellular level basic cell processes under contr...

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Autores principales: Pirnat, Samo, Božić, Mićo, Dolanc, Dorian, Horvat, Anemari, Tavčar, Petra, Vardjan, Nina, Verkhratsky, Alexei, Zorec, Robert, Stenovec, Matjaž
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290837/
https://www.ncbi.nlm.nih.gov/pubmed/34406698
http://dx.doi.org/10.1002/glia.24076
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author Pirnat, Samo
Božić, Mićo
Dolanc, Dorian
Horvat, Anemari
Tavčar, Petra
Vardjan, Nina
Verkhratsky, Alexei
Zorec, Robert
Stenovec, Matjaž
author_facet Pirnat, Samo
Božić, Mićo
Dolanc, Dorian
Horvat, Anemari
Tavčar, Petra
Vardjan, Nina
Verkhratsky, Alexei
Zorec, Robert
Stenovec, Matjaž
author_sort Pirnat, Samo
collection PubMed
description The plasticity of astrocytes is fundamental for their principal function, maintaining homeostasis of the central nervous system throughout life, and is associated with diverse exposomal challenges. Here, we used cultured astrocytes to investigate at subcellular level basic cell processes under controlled environmental conditions. We compared astroglial functional and signaling plasticity in standard serum‐containing growth medium, a condition mimicking pathologic conditions, and in medium without serum, favoring the acquisition of arborized morphology. Using opto−/electrophysiologic techniques, we examined cell viability, expression of astroglial markers, vesicle dynamics, and cytosolic Ca(2+) and cAMP signaling. The results revealed altered vesicle dynamics in arborized astrocytes that was associated with increased resting [Ca(2+)](i) and increased subcellular heterogeneity in [Ca(2+)](i), whereas [cAMP](i) subcellular dynamics remained stable in both cultures, indicating that cAMP signaling is less prone to plastic remodeling than Ca(2+) signaling, possibly also in in vivo contexts.
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spelling pubmed-92908372022-07-20 Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity Pirnat, Samo Božić, Mićo Dolanc, Dorian Horvat, Anemari Tavčar, Petra Vardjan, Nina Verkhratsky, Alexei Zorec, Robert Stenovec, Matjaž Glia Research Articles The plasticity of astrocytes is fundamental for their principal function, maintaining homeostasis of the central nervous system throughout life, and is associated with diverse exposomal challenges. Here, we used cultured astrocytes to investigate at subcellular level basic cell processes under controlled environmental conditions. We compared astroglial functional and signaling plasticity in standard serum‐containing growth medium, a condition mimicking pathologic conditions, and in medium without serum, favoring the acquisition of arborized morphology. Using opto−/electrophysiologic techniques, we examined cell viability, expression of astroglial markers, vesicle dynamics, and cytosolic Ca(2+) and cAMP signaling. The results revealed altered vesicle dynamics in arborized astrocytes that was associated with increased resting [Ca(2+)](i) and increased subcellular heterogeneity in [Ca(2+)](i), whereas [cAMP](i) subcellular dynamics remained stable in both cultures, indicating that cAMP signaling is less prone to plastic remodeling than Ca(2+) signaling, possibly also in in vivo contexts. John Wiley & Sons, Inc. 2021-08-18 2021-12 /pmc/articles/PMC9290837/ /pubmed/34406698 http://dx.doi.org/10.1002/glia.24076 Text en © 2021 The Authors. GLIA published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Pirnat, Samo
Božić, Mićo
Dolanc, Dorian
Horvat, Anemari
Tavčar, Petra
Vardjan, Nina
Verkhratsky, Alexei
Zorec, Robert
Stenovec, Matjaž
Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity
title Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity
title_full Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity
title_fullStr Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity
title_full_unstemmed Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity
title_short Astrocyte arborization enhances Ca(2+) but not cAMP signaling plasticity
title_sort astrocyte arborization enhances ca(2+) but not camp signaling plasticity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290837/
https://www.ncbi.nlm.nih.gov/pubmed/34406698
http://dx.doi.org/10.1002/glia.24076
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