The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains

Sigma 1 receptor (S1R) is a 223-amino-acid-long transmembrane endoplasmic reticulum (ER) protein. S1R modulates activity of multiple effector proteins and is a well-established drug target. However, signaling functions of S1R in cells are poorly understood. Here, we test the hypothesis that biologic...

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Main Authors: Vladimir Zhemkov, Jonathon A Ditlev, Wan-Ru Lee, Mikaela Wilson, Jen Liou, Michael K Rosen, Ilya Bezprozvanny
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-05-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/65192
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author Vladimir Zhemkov
Jonathon A Ditlev
Wan-Ru Lee
Mikaela Wilson
Jen Liou
Michael K Rosen
Ilya Bezprozvanny
author_facet Vladimir Zhemkov
Jonathon A Ditlev
Wan-Ru Lee
Mikaela Wilson
Jen Liou
Michael K Rosen
Ilya Bezprozvanny
author_sort Vladimir Zhemkov
collection DOAJ
description Sigma 1 receptor (S1R) is a 223-amino-acid-long transmembrane endoplasmic reticulum (ER) protein. S1R modulates activity of multiple effector proteins and is a well-established drug target. However, signaling functions of S1R in cells are poorly understood. Here, we test the hypothesis that biological activity of S1R in cells can be explained by its ability to interact with cholesterol and to form cholesterol-enriched microdomains in the ER membrane. By performing experiments in reduced reconstitution systems, we demonstrate direct effects of cholesterol on S1R clustering. We identify a novel cholesterol-binding motif in the transmembrane region of human S1R. Mutations of this motif impair association of recombinant S1R with cholesterol beads, affect S1R clustering in vitro and disrupt S1R subcellular localization. We demonstrate that S1R-induced membrane microdomains have increased local membrane thickness and that increased local cholesterol concentration and/or membrane thickness in these microdomains can modulate signaling of inositol-requiring enzyme 1α in the ER. Further, S1R agonists cause disruption of S1R clusters, suggesting that biological activity of S1R agonists is linked to remodeling of ER membrane microdomains. Our results provide novel insights into S1R-mediated signaling mechanisms in cells.
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spelling doaj.art-151f396a8d22489085371cbc83db875d2022-12-22T02:01:22ZengeLife Sciences Publications LtdeLife2050-084X2021-05-011010.7554/eLife.65192The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomainsVladimir Zhemkov0https://orcid.org/0000-0002-6554-1938Jonathon A Ditlev1https://orcid.org/0000-0001-8287-7700Wan-Ru Lee2Mikaela Wilson3Jen Liou4https://orcid.org/0000-0003-1546-3115Michael K Rosen5https://orcid.org/0000-0002-0775-7917Ilya Bezprozvanny6https://orcid.org/0000-0001-7006-6951Department of Physiology, UT Southwestern Medical Center at Dallas, Dallas, United StatesDepartment of Biophysics, Howard Hughes Medical Institute, UT Southwestern Medical Center at Dallas, Dallas, United StatesDepartment of Physiology, UT Southwestern Medical Center at Dallas, Dallas, United StatesDepartment of Physiology, UT Southwestern Medical Center at Dallas, Dallas, United StatesDepartment of Physiology, UT Southwestern Medical Center at Dallas, Dallas, United StatesDepartment of Biophysics, Howard Hughes Medical Institute, UT Southwestern Medical Center at Dallas, Dallas, United StatesDepartment of Physiology, UT Southwestern Medical Center at Dallas, Dallas, United States; Laboratory of Molecular Neurodegeneration, Peter the Great St. Petersburg State Polytechnic University, St. Petersburg, Russian FederationSigma 1 receptor (S1R) is a 223-amino-acid-long transmembrane endoplasmic reticulum (ER) protein. S1R modulates activity of multiple effector proteins and is a well-established drug target. However, signaling functions of S1R in cells are poorly understood. Here, we test the hypothesis that biological activity of S1R in cells can be explained by its ability to interact with cholesterol and to form cholesterol-enriched microdomains in the ER membrane. By performing experiments in reduced reconstitution systems, we demonstrate direct effects of cholesterol on S1R clustering. We identify a novel cholesterol-binding motif in the transmembrane region of human S1R. Mutations of this motif impair association of recombinant S1R with cholesterol beads, affect S1R clustering in vitro and disrupt S1R subcellular localization. We demonstrate that S1R-induced membrane microdomains have increased local membrane thickness and that increased local cholesterol concentration and/or membrane thickness in these microdomains can modulate signaling of inositol-requiring enzyme 1α in the ER. Further, S1R agonists cause disruption of S1R clusters, suggesting that biological activity of S1R agonists is linked to remodeling of ER membrane microdomains. Our results provide novel insights into S1R-mediated signaling mechanisms in cells.https://elifesciences.org/articles/65192sigma-1 receptorendoplasmic reticulumcholesterolmitochondria-associated membraneslipid microdomainsneurodegeneration
spellingShingle Vladimir Zhemkov
Jonathon A Ditlev
Wan-Ru Lee
Mikaela Wilson
Jen Liou
Michael K Rosen
Ilya Bezprozvanny
The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
eLife
sigma-1 receptor
endoplasmic reticulum
cholesterol
mitochondria-associated membranes
lipid microdomains
neurodegeneration
title The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
title_full The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
title_fullStr The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
title_full_unstemmed The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
title_short The role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
title_sort role of sigma 1 receptor in organization of endoplasmic reticulum signaling microdomains
topic sigma-1 receptor
endoplasmic reticulum
cholesterol
mitochondria-associated membranes
lipid microdomains
neurodegeneration
url https://elifesciences.org/articles/65192
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