Trichostatin A and vorinostat promote adipogenic differentiation through H3K9 acetylation and dimethylation

Res Vet Sci. 2019 Oct:126:207-212. doi: 10.1016/j.rvsc.2019.09.002. Epub 2019 Sep 12.

Abstract

To explore the effect of epigenetic modification on the differentiation of goat adipose-derived stem cells in vitro, we used two common epigenetic modification inhibitors, trichostatin A and vorinostat, to treat cashmere goat adipose-derived stem cells and induce adipocyte differentiation. The results showed that trichostatin A and vorinostat changed the relative amounts of H3K9 acetylation and dimethylation in the upstream sequence of PPARG, increased peroxisome proliferator-activated receptor gamma (PPARG) transcription before differentiation and then promoted adipocyte differentiation, and regulated the expression of adipocyte-specific genes. We conclude that adipocyte differentiation is regulated dynamically by different histone modifications. The areas of acetylation and demethylation changed by trichostatin A and vorinostat are the basis for further research on the mechanism of PPARG promoter to regulate adipocytes differentiation and provide research theroies for using adipose-derived stem cells as donor to produce transgenic animals to improve meat quality improvement.

Keywords: Acetylation; Adipogenic differentiation; Adipose-derived stem cells; Dimethylation; Goat.

MeSH terms

  • Acetylation / drug effects
  • Adipocytes / drug effects
  • Adipocytes / physiology
  • Adipogenesis / drug effects*
  • Animals
  • Epigenesis, Genetic / drug effects*
  • Goats / physiology*
  • Histone Deacetylase Inhibitors / pharmacology*
  • Hydroxamic Acids / pharmacology*
  • Methylation / drug effects
  • PPAR gamma / metabolism
  • Promoter Regions, Genetic / drug effects
  • Stem Cells / drug effects
  • Stem Cells / physiology
  • Vorinostat / pharmacology*

Substances

  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • PPAR gamma
  • trichostatin A
  • Vorinostat