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

期刊

GENES & DEVELOPMENT
卷 34, 期 5-6, 页码 321-340

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.334284.119

关键词

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

资金

  1. Nemzeti Kutatasi, Fejlesztesi es Innovacios Hivatal (NKFIH) [K123975, PD121138, GINOP-2.3.2-15-2016-00006]
  2. Hungarian Academy of Sciences [NKM-26/2019]
  3. Higher Education Institutional Excellence Program of the Ministry of Innovation and Technology in Hungary of the University of Debrecen [NKFIH-1150-6/2019]

向作者/读者索取更多资源

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.

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