MiR-145 reduces the activity of PI3K/Akt and MAPK signaling pathways and inhibits adipogenesis in bovine preadipocytes

Genomics. 2020 Jul;112(4):2688-2694. doi: 10.1016/j.ygeno.2020.02.020. Epub 2020 Mar 3.

Abstract

Adipose tissue is the largest metabolic organ because of adipogenesis controlled by numerous miRNAs. MiR-145 is classified into the same cluster with famous miR-143. However, few studies have investigated the role of miR-145 in adipogenesis. In the current study, we observed that the expression of miR-145 was downregulated during bovine adipogenesis in vivo and in vitro. The results of RNA-Seq analysis showed that miR-145 mainly disturb the PI3K/Akt and MAPK signaling pathways in bovine preadipocytes. MiR-145 inhibited bovine preadipocyte differentiation and downregulated phosphorylation level of Akt and ERK1/2 proteins. Furthermore, insulin, as a powerful inducer initiating adipogenesis and an activator of the PI3K/Akt and MAPK signaling pathways, was able to rescue the downregulation of Akt and ERK1/2 phosphorylation levels caused by miR-145. Taken together, our findings suggest that miR-145 is a potent inhibitor of adipogenesis that may function by reducing the activity of PI3K/Akt and MAPK signaling pathways.

Keywords: Adipogenesis; Bovine preadipocytes; MAPK; PI3K/Akt; miR-145.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / enzymology
  • Adipocytes / metabolism
  • Adipogenesis / genetics*
  • Animals
  • Cattle / genetics
  • Cattle / metabolism*
  • Cells, Cultured
  • MAP Kinase Signaling System
  • MicroRNAs / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • RNA-Seq
  • Signal Transduction*
  • Stem Cells / enzymology
  • Stem Cells / metabolism

Substances

  • MicroRNAs
  • Proto-Oncogene Proteins c-akt