HDAC3-Selective Inhibition Activates Brown and Beige Fat Through PRDM16

Endocrinology. 2018 Jul 1;159(7):2520-2527. doi: 10.1210/en.2018-00257.

Abstract

It has been reported that class I histone deacetylase (HDAC) inhibition increases thermogenesis in fat, but adipocyte-specific Hdac3 deletions have presented inconsistent results. In this study, we observed that HDAC3 protein levels were lower in brown fat compared with inguinal subcutaneous adipose tissue, and they decreased in both fat depots upon cold exposure. PR domain-containing 16 (PRDM16) physically interacted with HDAC3, and treatment with HDAC3-selective inhibitor RGFP966 induced thermogenic gene expression in murine and human fat cultures. This induction was blunted in the absence of PRDM16. Our results provide evidence that HDAC3 is involved in thermogenesis, suggesting selective inhibition of HDAC3 in brown and beige fat might hold therapeutic potential for counteracting human obesity and metabolic disorders.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylamides / pharmacology
  • Adipose Tissue, Beige / drug effects
  • Adipose Tissue, Beige / metabolism*
  • Adipose Tissue, Brown / drug effects
  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Enzyme Inhibitors / pharmacology
  • Histone Deacetylases / genetics
  • Histone Deacetylases / metabolism*
  • Humans
  • Immunoblotting
  • Immunoprecipitation
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Phenylenediamines / pharmacology
  • Real-Time Polymerase Chain Reaction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Acrylamides
  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • PRDM16 protein, human
  • Phenylenediamines
  • Prdm16 protein, mouse
  • RGFP966
  • Transcription Factors
  • Histone Deacetylases
  • histone deacetylase 3