Sénéchal Charlotte, Fujita Ryo, Jamet Solène, Maiga Arhamatoulaye, Dort Junio, Orfi Zakaria, Dumont Nicolas A, Bouvier Michel, Crist Colin
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.
Department of Human Genetics, McGill University, 3640 University St., Montréal, QC H3A 0C7, Canada.
Cell Rep. 2022 Nov 15;41(7):111645. doi: 10.1016/j.celrep.2022.111645.
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.
骨骼肌中存在着一群静止的肌肉干细胞(MuSCs),它们在损伤后能使组织再生。在此,我们表明黏附性G蛋白偶联受体Gpr116对于MuSC库的长期维持至关重要。静止的MuSCs表达高水平的Gpr116,而在MuSC激活后其会迅速下调。缺乏Gpr116的MuSCs随着时间的推移会逐渐耗竭,并且自我更新存在缺陷。黏附性G蛋白偶联受体在其长的N末端胞外域中包含一个激动肽序列,称为“Stachel”序列。用GPR116 Stachel肽刺激MuSCs会延迟MuSC的激活和分化。GPR116的Stachel肽刺激会导致与β-抑制蛋白的强烈相互作用。刺激GPR116会增加β-抑制蛋白1的核定位,在细胞核中它与环磷酸腺苷反应元件结合蛋白相互作用以调节基因表达。总之,我们提出了一个模型,即GPR116通过β-抑制蛋白1的核功能来维持MuSC库。