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Updated: Aug 21, 2025

Isolation of Quiescent Stem Cell Populations from Individual Skeletal Muscles
Published on: December 9, 2022
The adhesion G-protein-coupled receptor Gpr116 is essential to maintain the skeletal muscle stem cell pool
Charlotte Sénéchal1, Ryo Fujita1, Solène Jamet2
1Department 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.
Abstract:
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.
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