PPARγ2 regulates lipogenesis and lipid accumulation in steatotic hepatocytes

SE Schadinger, NLR Bucher… - American Journal …, 2005 - journals.physiology.org
SE Schadinger, NLR Bucher, BM Schreiber, SR Farmer
American Journal of Physiology-Endocrinology and Metabolism, 2005journals.physiology.org
Peroxisome proliferator-activated receptor-γ (PPARγ) is considered to be one of the master
regulators of adipocyte differentiation. PPARγ2 is abundantly expressed in mature
adipocytes and is elevated in the livers of animals that develop fatty livers. The aim of this
study was to determine the ability of PPARγ2 to induce lipid accumulation in hepatocytes
and to delineate molecular mechanisms driving this process. The hepatic cell line AML-12
was used to generate a cell line stably expressing PPARγ2. Oil Red O staining revealed that …
Peroxisome proliferator-activated receptor-γ (PPARγ) is considered to be one of the master regulators of adipocyte differentiation. PPARγ2 is abundantly expressed in mature adipocytes and is elevated in the livers of animals that develop fatty livers. The aim of this study was to determine the ability of PPARγ2 to induce lipid accumulation in hepatocytes and to delineate molecular mechanisms driving this process. The hepatic cell line AML-12 was used to generate a cell line stably expressing PPARγ2. Oil Red O staining revealed that PPARγ2 induces lipid accumulation in hepatocytes. This phenotype is accompanied by a selective upregulation of several adipogenic and lipogenic genes including adipose differentiation-related protein (ADRP), adipocyte fatty acid-binding protein 4, sterol regulatory element-binding protein-1 (SREBP-1), fatty acid synthase (FAS), and acetyl-CoA carboxylase, genes whose expression levels are known to increase in steatotic livers of ob/ob mice. Furthermore, the PPARγ2-regulated induction of both SREBP-1 and FAS parallels an increase in de novo triacylglycerol synthesis in hepatocytes. Triacylglycerol synthesis and lipid accumulation are further enhanced by culturing hepatocytes with troglitazone in the absence of exogenous lipids. These results correspond with an increase in the lipid droplet protein, ADRP, and the data demonstrate that ADRP functions to coat lipid droplets in hepatocytes as observed by confocal microscopy. Taken together, these observations propose a role for PPARγ2 as an inducer of steatosis in hepatocytes and suggest that this phenomenon occurs through an induction of pathways regulating de novo lipid synthesis.
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