Your browser doesn't support javascript.
loading
Enhancer of zeste homolog 2 (EZH2) regulates adipocyte lipid metabolism independent of adipogenic differentiation: Role of apolipoprotein E.
Yiew, Nicole K H; Greenway, Charlotte; Zarzour, Abdalrahman; Ahmadieh, Samah; Goo, Brandee; Kim, David; Benson, Tyler W; Ogbi, Mourad; Tang, Yao Liang; Chen, Weiqin; Stepp, David; Patel, Vijay; Hilton, Renee; Lu, Xin-Yun; Hui, David Y; Kim, Ha Won; Weintraub, Neal L.
Afiliación
  • Yiew NKH; Department of Pharmacology and Toxicology, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Greenway C; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Zarzour A; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Medicine (Division of Cardiology), Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Ahmadieh S; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Medicine (Division of Cardiology), Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Goo B; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Medicine (Division of Cardiology), Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Kim D; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Benson TW; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Ogbi M; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Tang YL; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Medicine (Division of Cardiology), Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Chen W; Department of Physiology, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Stepp D; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Physiology, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Patel V; Department of Cardiothoracic and Vascular Surgery, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Hilton R; Department of Minimally Invasive and Digestive Diseases Surgery, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Lu XY; Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Hui DY; Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio 45267.
  • Kim HW; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Medicine (Division of Cardiology), Medical College of Georgia at Augusta University, Augusta, Georgia 30912.
  • Weintraub NL; Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia 30912; Department of Medicine (Division of Cardiology), Medical College of Georgia at Augusta University, Augusta, Georgia 30912. Electronic address: nweintraub@augusta.edu.
J Biol Chem ; 294(21): 8577-8591, 2019 05 24.
Article en En | MEDLINE | ID: mdl-30971429
ABSTRACT
Enhancer of zeste homolog 2 (EZH2), an epigenetic regulator that plays a key role in cell differentiation and oncogenesis, was reported to promote adipogenic differentiation in vitro by catalyzing trimethylation of histone 3 lysine 27. However, inhibition of EZH2 induced lipid accumulation in certain cancer and hepatocyte cell lines. To address this discrepancy, we investigated the role of EZH2 in adipogenic differentiation and lipid metabolism using primary human and mouse preadipocytes and adipose-specific EZH2 knockout (KO) mice. We found that the EZH2-selective inhibitor GSK126 induced lipid accumulation in human adipocytes, without altering adipocyte differentiation marker gene expression. Moreover, adipocyte-specific EZH2 KO mice, generated by crossing EZH2 floxed mice with adiponectin-Cre mice, displayed significantly increased body weight, adipose tissue mass, and adipocyte cell size and reduced very low-density lipoprotein (VLDL) levels, as compared with littermate controls. These phenotypic alterations could not be explained by differences in feeding behavior, locomotor activity, metabolic energy expenditure, or adipose lipolysis. In addition, human adipocytes treated with either GSK126 or vehicle exhibited comparable rates of glucose-stimulated triglyceride accumulation and fatty acid uptake. Mechanistically, lipid accumulation induced by GSK126 in adipocytes was lipoprotein-dependent, and EZH2 inhibition or gene deletion promoted lipoprotein-dependent lipid uptake in vitro concomitant with up-regulated apolipoprotein E (ApoE) gene expression. Deletion of ApoE blocked the effects of GSK126 to promote lipoprotein-dependent lipid uptake in murine adipocytes. Collectively, these results indicate that EZH2 inhibition promotes lipoprotein-dependent lipid accumulation via inducing ApoE expression in adipocytes, suggesting a novel mechanism of lipid regulation by EZH2.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Apolipoproteínas E / Diferenciación Celular / Adipocitos / Lipogénesis / Proteína Potenciadora del Homólogo Zeste 2 / Lipólisis Límite: Animals / Humans Idioma: En Revista: J Biol Chem Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Apolipoproteínas E / Diferenciación Celular / Adipocitos / Lipogénesis / Proteína Potenciadora del Homólogo Zeste 2 / Lipólisis Límite: Animals / Humans Idioma: En Revista: J Biol Chem Año: 2019 Tipo del documento: Article