miR-130b inhibits proliferation and promotes differentiation in myocytes via targeting Sp1

J Mol Cell Biol. 2021 Sep 11;13(6):422-432. doi: 10.1093/jmcb/mjab012.

Abstract

Muscle regeneration after damage or during myopathies requires a fine cooperation between myoblast proliferation and myogenic differentiation. A growing body of evidence suggests that microRNAs play critical roles in myocyte proliferation and differentiation transcriptionally. However, the molecular mechanisms underlying the orchestration are not fully understood. Here, we showed that miR-130b is able to repress myoblast proliferation and promote myogenic differentiation via targeting Sp1 transcription factor. Importantly, overexpression of miR-130b is capable of improving the recovery of damaged muscle in a freeze injury model. Moreover, miR-130b expression is declined in the muscle of muscular dystrophy patients. Thus, these results indicated that miR-130b may play a role in skeletal muscle regeneration and myopathy progression. Together, our findings suggest that the miR-130b/Sp1 axis may serve as a potential therapeutic target for the treatment of patients with muscle damage or severe myopathies.

Keywords: Sp1; differentiation; miR-130b; muscle regeneration; proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics*
  • Cell Line
  • Cell Proliferation / genetics*
  • HEK293 Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics*
  • Muscle Cells / physiology*
  • Muscle Development / physiology
  • Muscles / physiology
  • Myoblasts / physiology
  • Sp1 Transcription Factor / genetics*

Substances

  • MIRN130 microRNA, human
  • MicroRNAs
  • Sp1 Transcription Factor
  • SP1 protein, human