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Calcium signaling as a mediator of cell energy demand and a trigger to cell death

Calcium signaling is pivotal to a host of physiological pathways. A rise in calcium concentration almost invariably signals an increased cellular energy demand. Consistent with this, calcium signals mediate a number of pathways that together serve to balance energy supply and demand. In pathological...

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Detalles Bibliográficos
Autores principales: Bhosale, Gauri, Sharpe, Jenny A., Sundier, Stephanie Y., Duchen, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949562/
https://www.ncbi.nlm.nih.gov/pubmed/26375864
http://dx.doi.org/10.1111/nyas.12885
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author Bhosale, Gauri
Sharpe, Jenny A.
Sundier, Stephanie Y.
Duchen, Michael R.
author_facet Bhosale, Gauri
Sharpe, Jenny A.
Sundier, Stephanie Y.
Duchen, Michael R.
author_sort Bhosale, Gauri
collection PubMed
description Calcium signaling is pivotal to a host of physiological pathways. A rise in calcium concentration almost invariably signals an increased cellular energy demand. Consistent with this, calcium signals mediate a number of pathways that together serve to balance energy supply and demand. In pathological states, calcium signals can precipitate mitochondrial injury and cell death, especially when coupled to energy depletion and oxidative or nitrosative stress. This review explores the mechanisms that couple cell signaling pathways to metabolic regulation or to cell death. The significance of these pathways is exemplified by pathological case studies, such as those showing loss of mitochondrial calcium uptake 1 in patients and ischemia/reperfusion injury.
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spelling pubmed-49495622016-07-28 Calcium signaling as a mediator of cell energy demand and a trigger to cell death Bhosale, Gauri Sharpe, Jenny A. Sundier, Stephanie Y. Duchen, Michael R. Ann N Y Acad Sci Original Articles Calcium signaling is pivotal to a host of physiological pathways. A rise in calcium concentration almost invariably signals an increased cellular energy demand. Consistent with this, calcium signals mediate a number of pathways that together serve to balance energy supply and demand. In pathological states, calcium signals can precipitate mitochondrial injury and cell death, especially when coupled to energy depletion and oxidative or nitrosative stress. This review explores the mechanisms that couple cell signaling pathways to metabolic regulation or to cell death. The significance of these pathways is exemplified by pathological case studies, such as those showing loss of mitochondrial calcium uptake 1 in patients and ischemia/reperfusion injury. John Wiley and Sons Inc. 2015-09-16 2015-09 /pmc/articles/PMC4949562/ /pubmed/26375864 http://dx.doi.org/10.1111/nyas.12885 Text en © 2015 The Authors. Annals of the New York Academy of Sciences published by Wiley Periodicals Inc. on behalf of The New York Academy of Sciences. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bhosale, Gauri
Sharpe, Jenny A.
Sundier, Stephanie Y.
Duchen, Michael R.
Calcium signaling as a mediator of cell energy demand and a trigger to cell death
title Calcium signaling as a mediator of cell energy demand and a trigger to cell death
title_full Calcium signaling as a mediator of cell energy demand and a trigger to cell death
title_fullStr Calcium signaling as a mediator of cell energy demand and a trigger to cell death
title_full_unstemmed Calcium signaling as a mediator of cell energy demand and a trigger to cell death
title_short Calcium signaling as a mediator of cell energy demand and a trigger to cell death
title_sort calcium signaling as a mediator of cell energy demand and a trigger to cell death
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949562/
https://www.ncbi.nlm.nih.gov/pubmed/26375864
http://dx.doi.org/10.1111/nyas.12885
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