Emerging roles of histone deacetylases in adaptive thermogenesis

Front Endocrinol (Lausanne). 2023 Feb 16:14:1124408. doi: 10.3389/fendo.2023.1124408. eCollection 2023.

Abstract

Brown and beige adipose tissues regulate body energy expenditure through adaptive thermogenesis, which converts energy into heat by oxidative phosphorylation uncoupling. Although promoting adaptive thermogenesis has been demonstrated to be a prospective strategy for obesity control, there are few methods for increasing adipose tissue thermogenesis in a safe and effective way. Histone deacetylase (HDAC) is a category of epigenetic modifying enzymes that catalyzes deacetylation on both histone and non-histone proteins. Recent studies illustrated that HDACs play an important role in adipose tissue thermogenesis through modulating gene transcription and chromatin structure as well as cellular signals transduction in both deacetylation dependent or independent manners. Given that different classes and subtypes of HDACs show diversity in the mechanisms of adaptive thermogenesis regulation, we systematically summarized the effects of different HDACs on adaptive thermogenesis and their underlying mechanisms in this review. We also emphasized the differences among HDACs in thermogenesis regulation, which will help to find new efficient anti-obesity drugs targeting specific HDAC subtypes.

Keywords: adaptive thermogenesis; adipose tissue; diabetes; histone deacetylase; obesity.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue*
  • Adipose Tissue, Beige
  • Anti-Obesity Agents*
  • Histone Deacetylases
  • Thermogenesis

Substances

  • Anti-Obesity Agents
  • Histone Deacetylases

Grants and funding

This study was supported by the National Natural Science Foundation of China (grant numbers 81873060 and 81473391) and the open projects of the discipline of Chinese Medicine of Nanjing University of Chinese Medicine supported by the subject of academic priority discipline of Jiangsu Higher Education Institutions (ZYX03KF058).