A Novel Mechanism of bta-miR-210 in Bovine Early Intramuscular Adipogenesis

Genes (Basel). 2020 May 29;11(6):601. doi: 10.3390/genes11060601.

Abstract

Intramuscular fat (IMF) is one of the major factors determining beef quality. IMF formation is influenced by multiple conditions including genetic background, age and nutrition. In our previous investigation, bta-miR-210 was found to be increased during adipogenesis using miRNA-seq. In this study, we validated the upregulation of bta-miR-210 in platelet-derived growth factor receptor α positive (PDGFRα+) progenitor cells during adipogenic differentiation in vitro. To investigate its role in adipogenesis, bta-miR-210 mimics were introduced into progenitor cells, which resulted in enhanced intracellular lipid accumulation. Accordingly, the expression of adipocyte-specific genes significantly increased in the bta-miR-210 mimic group compared to that in the negative control group (p < 0.01). Dual-luciferase reporter assays revealed that WISP2 is a target of bta-miR-210. WISP2 knockdown enhanced adipogenesis. In conclusion, bta-miR-210 positively regulates the adipogenesis of PDGFRα+ cells derived from bovine fetal muscle by targeting WISP2.

Keywords: WISP2; bovine; bta-miR-210; intramuscular adipogenesis; progenitor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipocytes / pathology
  • Adipogenesis / genetics*
  • Animals
  • CCN Intercellular Signaling Proteins / genetics*
  • Cattle
  • Cell Differentiation / genetics
  • MicroRNAs / genetics*
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism*
  • Receptor, Platelet-Derived Growth Factor alpha
  • Stem Cells / metabolism

Substances

  • CCN Intercellular Signaling Proteins
  • MicroRNAs
  • Receptor, Platelet-Derived Growth Factor alpha