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The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival

Ca(2+) is an important second messenger participating in many cellular activities; when physicochemical insults deregulate its delicate homeostasis, it acts as an intrinsic stressor, producing/increasing cell damage. Damage elicits both repair and death responses; intriguingly, in those responses Ca...

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Detalles Bibliográficos
Autores principales: Cerella, Claudia, Diederich, Marc, Ghibelli, Lina
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838366/
https://www.ncbi.nlm.nih.gov/pubmed/20300548
http://dx.doi.org/10.1155/2010/546163
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author Cerella, Claudia
Diederich, Marc
Ghibelli, Lina
author_facet Cerella, Claudia
Diederich, Marc
Ghibelli, Lina
author_sort Cerella, Claudia
collection PubMed
description Ca(2+) is an important second messenger participating in many cellular activities; when physicochemical insults deregulate its delicate homeostasis, it acts as an intrinsic stressor, producing/increasing cell damage. Damage elicits both repair and death responses; intriguingly, in those responses Ca(2+) also participates as second messenger. This delineates a dual role for Ca(2+) in cell stress, making difficult to separate the different and multiple mechanisms required for Ca(2+)-mediated control of cell survival and apoptosis. Here we attempt to disentangle the two scenarios, examining on the one side, the events implicated in deregulated Ca(2+) toxicity and the mechanisms through which this elicits reparative or death pathways; on the other, reviewing the role of Ca(2+) as a messenger in the transduction of these same signaling events.
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spelling pubmed-28383662010-03-18 The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival Cerella, Claudia Diederich, Marc Ghibelli, Lina Int J Cell Biol Review Article Ca(2+) is an important second messenger participating in many cellular activities; when physicochemical insults deregulate its delicate homeostasis, it acts as an intrinsic stressor, producing/increasing cell damage. Damage elicits both repair and death responses; intriguingly, in those responses Ca(2+) also participates as second messenger. This delineates a dual role for Ca(2+) in cell stress, making difficult to separate the different and multiple mechanisms required for Ca(2+)-mediated control of cell survival and apoptosis. Here we attempt to disentangle the two scenarios, examining on the one side, the events implicated in deregulated Ca(2+) toxicity and the mechanisms through which this elicits reparative or death pathways; on the other, reviewing the role of Ca(2+) as a messenger in the transduction of these same signaling events. Hindawi Publishing Corporation 2010 2010-03-15 /pmc/articles/PMC2838366/ /pubmed/20300548 http://dx.doi.org/10.1155/2010/546163 Text en Copyright © 2010 Claudia Cerella et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Cerella, Claudia
Diederich, Marc
Ghibelli, Lina
The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival
title The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival
title_full The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival
title_fullStr The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival
title_full_unstemmed The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival
title_short The Dual Role of Calcium as Messenger and Stressor in Cell Damage, Death, and Survival
title_sort dual role of calcium as messenger and stressor in cell damage, death, and survival
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838366/
https://www.ncbi.nlm.nih.gov/pubmed/20300548
http://dx.doi.org/10.1155/2010/546163
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