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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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Detalles Bibliográficos
Autor principal: Hayashi, Teruo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
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
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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.
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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
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