The adhesion G-protein-coupled receptor Gpr116 is essential to maintain the skeletal muscle stem cell pool.

CP: Stem cell research GPR116 adhesion G-protein-coupled receptor muscle stem cell regeneration skeletal muscle β-arrestin1

Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
15 11 2022
Historique:
received: 29 11 2021
revised: 26 08 2022
accepted: 19 10 2022
entrez: 17 11 2022
pubmed: 18 11 2022
medline: 22 11 2022
Statut: ppublish

Résumé

Skeletal muscle is populated with a reservoir of quiescent muscle stem cells (MuSCs), which regenerate the tissue after injury. Here, we show that the adhesion G-protein-coupled receptor Gpr116 is essential for long-term maintenance of the MuSC pool. Quiescent MuSCs express high levels of Gpr116, which is rapidly downregulated upon MuSC activation. MuSCs deficient for Gpr116 exhibit progressive depletion over time and are defective in self-renewal. Adhesion G-protein-coupled receptors contain an agonistic peptide sequence, called the "Stachel" sequence, within their long N-terminal ectodomains. Stimulation of MuSCs with the GPR116 Stachel peptide delays MuSC activation and differentiation. Stachel peptide stimulation of GPR116 leads to strong interaction with β-arrestins. Stimulation of GPR116 increases the nuclear localization of β-arrestin1, where it interacts with cAMP response element binding protein to regulate gene expression. Altogether, we propose a model by which GPR116 maintains the MuSC pool via nuclear functions of β-arrestin1.

Identifiants

pubmed: 36384129
pii: S2211-1247(22)01516-9
doi: 10.1016/j.celrep.2022.111645
pii:
doi:

Substances chimiques

Receptors, G-Protein-Coupled 0
Peptides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

111645

Subventions

Organisme : CIHR
ID : FDN-148431
Pays : Canada
Organisme : CIHR
ID : 399258
Pays : Canada
Organisme : CIHR
ID : 479222
Pays : Canada

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Charlotte Sénéchal (C)

Department of Human Genetics, McGill University, 3640 University St., Montréal, QC H3A 0C7, Canada; Lady Davis Institute for Medical Research, Jewish General Hospital, 3755 chemin de la Cote Ste. Catherine, Montréal, QC H3T 1E2, Canada.

Ryo Fujita (R)

Department of Human Genetics, McGill University, 3640 University St., Montréal, QC H3A 0C7, Canada; Lady Davis Institute for Medical Research, Jewish General Hospital, 3755 chemin de la Cote Ste. Catherine, Montréal, QC H3T 1E2, Canada.

Solène Jamet (S)

Department of Human Genetics, McGill University, 3640 University St., Montréal, QC H3A 0C7, Canada.

Arhamatoulaye Maiga (A)

Department of Biochemistry and Molecular Medicine, Institute for Research in Immunology and Cancer (IRIC), Université de Montréal, Montréal, QC H3T 1J4, Canada.

Junio Dort (J)

CHU Sainte-Justine Research Center, Montréal, QC, Canada.

Zakaria Orfi (Z)

CHU Sainte-Justine Research Center, Montréal, QC, Canada.

Nicolas A Dumont (NA)

CHU Sainte-Justine Research Center, Montréal, QC, Canada; Université de Montréal, Faculty of Medicine, School of Rehabilitation, Montréal, QC, Canada.

Michel Bouvier (M)

Department of Biochemistry and Molecular Medicine, Institute for Research in Immunology and Cancer (IRIC), Université de Montréal, Montréal, QC H3T 1J4, Canada.

Colin Crist (C)

Department of Human Genetics, McGill University, 3640 University St., Montréal, QC H3A 0C7, Canada; Lady Davis Institute for Medical Research, Jewish General Hospital, 3755 chemin de la Cote Ste. Catherine, Montréal, QC H3T 1E2, Canada. Electronic address: colin.crist@mcgill.ca.

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Classifications MeSH