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The Sigma-1 Receptor in Cellular Stress Signaling
After decades of research, the sigma-1 receptor (Sig-1R)’s structure, and molecular functions are being unveiled. Sig-1R is an integral endoplasmic reticulum (ER) membrane protein which forms an oligomer and binds a variety of psychotropic drugs. It forms a complex with the ER chaperone BiP that con...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646578/ https://www.ncbi.nlm.nih.gov/pubmed/31379486 http://dx.doi.org/10.3389/fnins.2019.00733 |
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author | Hayashi, Teruo |
author_facet | Hayashi, Teruo |
author_sort | Hayashi, Teruo |
collection | PubMed |
description | After decades of research, the sigma-1 receptor (Sig-1R)’s structure, and molecular functions are being unveiled. Sig-1R is an integral endoplasmic reticulum (ER) membrane protein which forms an oligomer and binds a variety of psychotropic drugs. It forms a complex with the ER chaperone BiP that controls specific signaling molecules’ stability and function at the ER to regulate Ca(2+) signaling, bioenergetics, and ER stress. Sig-1R is highly enriched in ER subdomains that are physically linked to outer mitochondrial membranes, reflecting its role in regulating ER–mitochondria communications. Thus, Sig-1R ligands are expected to serve as novel neuroprotective agents which treat certain psychiatric and neurodegenerative disorders. In this short review, the cell biological aspects of Sig-1R are discussed, with a particular focus on its role in fundamental ER functions. |
format | Online Article Text |
id | pubmed-6646578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66465782019-08-02 The Sigma-1 Receptor in Cellular Stress Signaling Hayashi, Teruo Front Neurosci Neuroscience After decades of research, the sigma-1 receptor (Sig-1R)’s structure, and molecular functions are being unveiled. Sig-1R is an integral endoplasmic reticulum (ER) membrane protein which forms an oligomer and binds a variety of psychotropic drugs. It forms a complex with the ER chaperone BiP that controls specific signaling molecules’ stability and function at the ER to regulate Ca(2+) signaling, bioenergetics, and ER stress. Sig-1R is highly enriched in ER subdomains that are physically linked to outer mitochondrial membranes, reflecting its role in regulating ER–mitochondria communications. Thus, Sig-1R ligands are expected to serve as novel neuroprotective agents which treat certain psychiatric and neurodegenerative disorders. In this short review, the cell biological aspects of Sig-1R are discussed, with a particular focus on its role in fundamental ER functions. Frontiers Media S.A. 2019-07-16 /pmc/articles/PMC6646578/ /pubmed/31379486 http://dx.doi.org/10.3389/fnins.2019.00733 Text en Copyright © 2019 Hayashi. http://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 | Neuroscience Hayashi, Teruo The Sigma-1 Receptor in Cellular Stress Signaling |
title | The Sigma-1 Receptor in Cellular Stress Signaling |
title_full | The Sigma-1 Receptor in Cellular Stress Signaling |
title_fullStr | The Sigma-1 Receptor in Cellular Stress Signaling |
title_full_unstemmed | The Sigma-1 Receptor in Cellular Stress Signaling |
title_short | The Sigma-1 Receptor in Cellular Stress Signaling |
title_sort | sigma-1 receptor in cellular stress signaling |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6646578/ https://www.ncbi.nlm.nih.gov/pubmed/31379486 http://dx.doi.org/10.3389/fnins.2019.00733 |
work_keys_str_mv | AT hayashiteruo thesigma1receptorincellularstresssignaling AT hayashiteruo sigma1receptorincellularstresssignaling |