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MicroRNA-24-3p promotes skeletal muscle differentiation and regeneration by regulating HMGA1.

Paromita DeyMiles A SoyerBijan K Dey
Published in: Cellular and molecular life sciences : CMLS (2022)
Numerous studies have established the critical roles of microRNAs in regulating post-transcriptional gene expression in diverse biological processes. Here, we report on the role and mechanism of miR-24-3p in skeletal muscle differentiation and regeneration. miR-24-3p promotes myoblast differentiation and skeletal muscle regeneration by directly targeting high mobility group AT-hook 1 (HMGA1) and regulating it and its direct downstream target, the inhibitor of differentiation 3 (ID3). miR-24-3p knockdown in neonatal mice increases PAX7-positive proliferating muscle stem cells (MuSCs) by derepressing Hmga1 and Id3. Similarly, inhibition of miR-24-3p in the tibialis anterior muscle prevents Hmga1 and Id3 downregulation and impairs regeneration. These findings provide evidence that the miR-24-3p/HMGA1/ID3 axis is required for MuSC differentiation and skeletal muscle regeneration in vivo.
Keyphrases
  • skeletal muscle
  • stem cells
  • gene expression
  • insulin resistance
  • cell proliferation
  • mesenchymal stem cells
  • drug delivery
  • signaling pathway
  • adipose tissue
  • oxidative stress
  • heat shock