SESN3 Inhibited SMAD3 to Relieve Its Suppression for MiR-124, Thus Regulating Pre-Adipocyte Adipogenesis

Genes (Basel). 2021 Nov 23;12(12):1852. doi: 10.3390/genes12121852.

Abstract

Sestrin-3, together with the other two members Sestrin-1 and Sestrin-2, belongs to the Sestrin family. The Sestrin protein family has been demonstrated to be involved in antioxidative, metabolic homeostasis, and even the development of nonalcoholic steatohepatitis (NASH). However, the adipogenic regulatory role of SESN3 in adipogenesis still needs to be further explored. In this study, we demonstrated SESN3 inhibited porcine pre-adipocyte proliferation, thus suppressing its adipogenesis. Meanwhile, SESN3 has been demonstrated to inhibit Smad3 thus protecting against NASH. Further, for our previous study, we found mmu-miR-124 involved in 3T3-L1 cell adipogenesis regulation. In this study, we also identified that ssc-miR-124 inhibited porcine pre-adipocyte proliferation, thus suppressing its adipogenesis, and the SMAD3 was an inhibitor of ssc-miR-124 by binding to its promoter. Furthermore, the ssc-miR-124 targeted porcine C/EBPα and GR and thus inhibited pre-adipocyte adipogenesis. In conclusion, SESN3 inhibited SMAD3, thus improving ssc-miR124, and then suppressed C/EBPα and GR to regulate pre-adipocytes adipogenesis.

Keywords: SESN3; SMAD3; adipogenesis; pig; ssc-miR-124-3p.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / pathology*
  • Adipogenesis / genetics*
  • Animals
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Heat-Shock Proteins / genetics*
  • Mice
  • MicroRNAs / genetics*
  • Non-alcoholic Fatty Liver Disease / genetics
  • Smad3 Protein / genetics*

Substances

  • Heat-Shock Proteins
  • MicroRNAs
  • Mirn124 microRNA, mouse
  • Sesn3 protein, mouse
  • Smad3 Protein
  • Smad3 protein, mouse