MiR-183-5p induced by saturated fatty acids regulates the myogenic differentiation by directly targeting FHL1 in C2C12 myoblasts

BMB Rep. 2020 Nov;53(11):605-610. doi: 10.5483/BMBRep.2020.53.11.175.

Abstract

Skeletal myogenesis is a complex process that is finely regulated by myogenic transcription factors. Recent studies have shown that saturated fatty acids (SFA) can suppress the activation of myogenic transcription factors and impair the myogenic differentiation of progenitor cells. Despite the increasing evidence of the roles of miRNAs in myogenesis, the targets and myogenic regulatory mechanisms of miRNAs are largely unknown, particularly when myogenesis is dysregulated by SFA deposition. This study examined the implications of SFA-induced miR-183-5p on the myogenic differentiation in C2C12 myoblasts. Long-chain SFA palmitic acid (PA) drastically reduced myogenic transcription factors, such as myoblast determination protein (MyoD), myogenin (MyoG), and myocyte enhancer factor 2C (MEF2C), and inhibited FHL1 expression and myogenic differentiation of C2C12 myoblasts, accompanied by the induction of miR-183-5p. The knockdown of FHL1 by siRNA inhibited myogenic differentiation of myoblasts. Interestingly, miR-183-5p inversely regulated the expression of FHL1, a crucial regulator of skeletal myogenesis, by targeting the 3'UTR of FHL1 mRNA. Furthermore, the transfection of miR-183-5p mimic suppressed the expression of MyoD, MyoG, MEF2C, and MyHC, and impaired the differentiation and myotube formation of myoblasts. Overall, this study highlights the role of miR-183-5p in myogenic differentiation through FHL1 repression and suggests a novel miRNA-mediated mechanism for myogenesis in a background of obesity. [BMB Reports 2020; 53(11): 605-610].

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Line
  • Cell Proliferation / genetics
  • Fatty Acids / metabolism
  • Fatty Acids / pharmacology
  • Gene Expression / genetics
  • Gene Expression Regulation / genetics
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • LIM Domain Proteins / genetics*
  • LIM Domain Proteins / metabolism
  • MEF2 Transcription Factors / metabolism
  • Mice
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Muscle Development / genetics
  • Muscle Fibers, Skeletal / metabolism
  • Muscle Proteins / genetics*
  • Muscle Proteins / metabolism
  • Myoblasts / metabolism*
  • Myoblasts / physiology
  • Myogenin / metabolism
  • RNA, Messenger / metabolism

Substances

  • Fatty Acids
  • Fhl1 protein, mouse
  • Intracellular Signaling Peptides and Proteins
  • LIM Domain Proteins
  • MEF2 Transcription Factors
  • MicroRNAs
  • Mirn183 microRNA, mouse
  • Muscle Proteins
  • Myogenin
  • RNA, Messenger