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STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases
Tight spatiotemporal regulation of intracellular Ca(2+) plays a critical role in regulating diverse cellular functions including cell survival, metabolism, and transcription. As a result, eukaryotic cells have developed a wide variety of mechanisms for controlling Ca(2+) influx and efflux across the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261457/ https://www.ncbi.nlm.nih.gov/pubmed/35821821 http://dx.doi.org/10.3389/fragi.2022.876785 |
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author | Collins, Helen E. Zhang, Dingguo Chatham, John C. |
author_facet | Collins, Helen E. Zhang, Dingguo Chatham, John C. |
author_sort | Collins, Helen E. |
collection | PubMed |
description | Tight spatiotemporal regulation of intracellular Ca(2+) plays a critical role in regulating diverse cellular functions including cell survival, metabolism, and transcription. As a result, eukaryotic cells have developed a wide variety of mechanisms for controlling Ca(2+) influx and efflux across the plasma membrane as well as Ca(2+) release and uptake from intracellular stores. The STIM and Orai protein families comprising of STIM1, STIM2, Orai1, Orai2, and Orai3, are evolutionarily highly conserved proteins that are core components of all mammalian Ca(2+) signaling systems. STIM1 and Orai1 are considered key players in the regulation of Store Operated Calcium Entry (SOCE), where release of Ca(2+) from intracellular stores such as the Endoplasmic/Sarcoplasmic reticulum (ER/SR) triggers Ca(2+) influx across the plasma membrane. SOCE, which has been widely characterized in non-excitable cells, plays a central role in Ca(2+)-dependent transcriptional regulation. In addition to their role in Ca(2+) signaling, STIM1 and Orai1 have been shown to contribute to the regulation of metabolism and mitochondrial function. STIM and Orai proteins are also subject to redox modifications, which influence their activities. Considering their ubiquitous expression, there has been increasing interest in the roles of STIM and Orai proteins in excitable cells such as neurons and myocytes. While controversy remains as to the importance of SOCE in excitable cells, STIM1 and Orai1 are essential for cellular homeostasis and their disruption is linked to various diseases associated with aging such as cardiovascular disease and neurodegeneration. The recent identification of splice variants for most STIM and Orai isoforms while complicating our understanding of their function, may also provide insight into some of the current contradictions on their roles. Therefore, the goal of this review is to describe our current understanding of the molecular regulation of STIM and Orai proteins and their roles in normal physiology and diseases of aging, with a particular focus on heart disease and neurodegeneration. |
format | Online Article Text |
id | pubmed-9261457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92614572022-07-11 STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases Collins, Helen E. Zhang, Dingguo Chatham, John C. Front Aging Aging Tight spatiotemporal regulation of intracellular Ca(2+) plays a critical role in regulating diverse cellular functions including cell survival, metabolism, and transcription. As a result, eukaryotic cells have developed a wide variety of mechanisms for controlling Ca(2+) influx and efflux across the plasma membrane as well as Ca(2+) release and uptake from intracellular stores. The STIM and Orai protein families comprising of STIM1, STIM2, Orai1, Orai2, and Orai3, are evolutionarily highly conserved proteins that are core components of all mammalian Ca(2+) signaling systems. STIM1 and Orai1 are considered key players in the regulation of Store Operated Calcium Entry (SOCE), where release of Ca(2+) from intracellular stores such as the Endoplasmic/Sarcoplasmic reticulum (ER/SR) triggers Ca(2+) influx across the plasma membrane. SOCE, which has been widely characterized in non-excitable cells, plays a central role in Ca(2+)-dependent transcriptional regulation. In addition to their role in Ca(2+) signaling, STIM1 and Orai1 have been shown to contribute to the regulation of metabolism and mitochondrial function. STIM and Orai proteins are also subject to redox modifications, which influence their activities. Considering their ubiquitous expression, there has been increasing interest in the roles of STIM and Orai proteins in excitable cells such as neurons and myocytes. While controversy remains as to the importance of SOCE in excitable cells, STIM1 and Orai1 are essential for cellular homeostasis and their disruption is linked to various diseases associated with aging such as cardiovascular disease and neurodegeneration. The recent identification of splice variants for most STIM and Orai isoforms while complicating our understanding of their function, may also provide insight into some of the current contradictions on their roles. Therefore, the goal of this review is to describe our current understanding of the molecular regulation of STIM and Orai proteins and their roles in normal physiology and diseases of aging, with a particular focus on heart disease and neurodegeneration. Frontiers Media S.A. 2022-04-19 /pmc/articles/PMC9261457/ /pubmed/35821821 http://dx.doi.org/10.3389/fragi.2022.876785 Text en Copyright © 2022 Collins, Zhang and Chatham. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Aging Collins, Helen E. Zhang, Dingguo Chatham, John C. STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases |
title | STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases |
title_full | STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases |
title_fullStr | STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases |
title_full_unstemmed | STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases |
title_short | STIM and Orai Mediated Regulation of Calcium Signaling in Age-Related Diseases |
title_sort | stim and orai mediated regulation of calcium signaling in age-related diseases |
topic | Aging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9261457/ https://www.ncbi.nlm.nih.gov/pubmed/35821821 http://dx.doi.org/10.3389/fragi.2022.876785 |
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