Mst1/2 Is Necessary for Satellite Cell Differentiation to Promote Muscle Regeneration

Stem Cells. 2022 Mar 3;40(1):74-87. doi: 10.1093/stmcls/sxab010.

Abstract

The diminished ability for muscle to regenerate is associated with aging, diabetes, and cancers. Muscle regeneration depends on the activation and differentiation of satellite cells (SCs). Inactivation of Mst1/2 promotes cell proliferation by activating Yap, and that has been reported as a potential therapeutic target for improving many organ regeneration. However, the function of Mst1/2 in SCs fate decision and that effect on muscle regeneration remain unknown. By using inducible conditional knockout Mst1/2 in the SCs of mice and an inhibitor of Mst1/2, we found that inhibition of Mst1/2 in SCs significantly decrease Yap phosphorylation, thus causing Yap to accumulate in the nucleus and impairing SC differentiation; Mst1/2 were slightly elevated by irisin stimulation during SC differentiation; but inhibiting Mst1/2 in SCs significantly impaired irisin-induced muscle regeneration. These results indicate that Mst1/2 is necessary for SC differentiation and inhibiting Mst1/2 as a therapeutic target has potential risks for muscle regeneration.

Keywords: Irisin; Mst1/2; Yap; muscle regeneration; satellite cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation
  • Cell Proliferation
  • Muscle, Skeletal
  • Muscles
  • Myoblasts*
  • Satellite Cells, Skeletal Muscle*
  • Transcription Factors

Substances

  • Transcription Factors