The role of ADP-ribose metabolism in metabolic regulation, adipose tissue differentiation, and metabolism

Genes Dev. 2020 Mar 1;34(5-6):321-340. doi: 10.1101/gad.334284.119. Epub 2020 Feb 6.

Abstract

Poly(ADP-ribose) polymerases (PARPs or ARTDs), originally described as DNA repair factors, have metabolic regulatory roles. PARP1, PARP2, PARP7, PARP10, and PARP14 regulate central and peripheral carbohydrate and lipid metabolism and often channel pathological disruptive metabolic signals. PARP1 and PARP2 are crucial for adipocyte differentiation, including the commitment toward white, brown, or beige adipose tissue lineages, as well as the regulation of lipid accumulation. Through regulating adipocyte function and organismal energy balance, PARPs play a role in obesity and the consequences of obesity. These findings can be translated into humans, as evidenced by studies on identical twins and SNPs affecting PARP activity.

Keywords: AFLD; ARTD; NAFLD; PARP; PARylation; adipocyte; adipogenesis; atherosclerosis; beige adipocytes; brown adipocytes; differentiation; high fat diet; insulin resistance; lipolysis; mitochondria; obesity; stem cell; white adipocytes.

Publication types

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

MeSH terms

  • Adenosine Diphosphate Ribose / metabolism*
  • Adipose Tissue / cytology*
  • Adipose Tissue / metabolism*
  • Carbohydrate Metabolism
  • Cell Differentiation*
  • Humans
  • Lipid Metabolism / physiology
  • Poly(ADP-ribose) Polymerases / metabolism*

Substances

  • Adenosine Diphosphate Ribose
  • Poly(ADP-ribose) Polymerases