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Publication : Transcriptional activation of Fsp27 by the liver-enriched transcription factor CREBH promotes lipid droplet growth and hepatic steatosis.

First Author  Xu X Year  2015
Journal  Hepatology Volume  61
Issue  3 Pages  857-69
PubMed ID  25125366 Mgi Jnum  J:318255
Mgi Id  MGI:6858935 Doi  10.1002/hep.27371
Citation  Xu X, et al. (2015) Transcriptional activation of Fsp27 by the liver-enriched transcription factor CREBH promotes lipid droplet growth and hepatic steatosis. Hepatology 61(3):857-69
abstractText  UNLABELLED: Fat-specific protein 27 (Fsp27) is a lipid droplet-associated protein that promotes lipid droplet (LD) growth and triglyceride (TG) storage in white adipocytes. Fsp27 is also highly expressed in the steatotic liver and contributes to TG accumulation. In this study we discovered that the liver produces Fsp27beta, an alternative Fsp27 isoform, which contains 10 additional amino acids at the N-terminus of the original Fsp27 (Fsp27alpha). White adipose tissue (WAT) and the liver specifically expressed Fsp27alpha and Fsp27beta transcripts, respectively, which were driven by distinct promoters. The Fsp27beta promoter was activated by the liver-enriched transcription factor cyclic-AMP-responsive-element-binding protein H (CREBH) but not by peroxisome proliferator-activated receptor gamma (PPARgamma), which activated the Fsp27alpha promoter. Enforced expression of the constitutively active CREBH strongly induced Fsp27beta and the human ortholog CIDEC2 in mouse hepatocytes and HepG2 cells, respectively. In contrast, loss of CREBH decreased hepatic Fsp27beta in fasted mice, suggesting that CREBH plays a critical role in Fsp27beta expression in the liver. Similar to Fsp27alpha, Fsp27beta localized on the surface of lipid droplets and suppressed lipolysis. Consequently, enforced expression of Fsp27beta or CREBH promoted lipid droplet enlargement and TG accumulation in the liver. CONCLUSION: The CREBH-Fsp27beta axis is important for regulating lipid droplet dynamics and TG storage in the liver.
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