Fuchs Claudia D, Claudel Thierry, Scharnagl Hubert, Stojakovic Tatjana, Trauner Michael
Hans Popper Laboratory of Molecular Hepatology, Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Austria.
FEBS Lett. 2017 Oct;591(20):3360-3368. doi: 10.1002/1873-3468.12845. Epub 2017 Oct 11.
The farnesoid X receptor (FXR) and C/EBP homologous protein (CHOP) have critical functions in hepatic lipid metabolism. Here, we aimed to explore a potential relationship between FXR and CHOP. We fed wild-type (WT) and FXR KO mice a MCD diet (model of steatohepatitis) and found that Chop mRNA expression is upregulated in WT but not FXR KO mice. The absence of FXR aggravates hepatic inflammation after MCD feeding. In HepG2 cells, we found that Chop expression is regulated in a FXR/Retinoid X receptor (RXR)-dependent manner. We identified a FXR/RXR-binding site in the human CHOP promoter, demonstrating a highly conserved regulatory pathway. Our study shows that FXR/RXR regulates Chop expression in a mouse model of steatohepatitis, providing novel insights into pathogenesis of this disorder.
法尼酯X受体(FXR)和C/EBP同源蛋白(CHOP)在肝脏脂质代谢中发挥关键作用。在此,我们旨在探究FXR与CHOP之间的潜在关系。我们给野生型(WT)和FXR基因敲除(KO)小鼠喂食蛋氨酸胆碱缺乏(MCD)饮食(一种脂肪性肝炎模型),发现Chop mRNA表达在WT小鼠中上调,但在FXR KO小鼠中未上调。FXR的缺失会加剧MCD喂养后的肝脏炎症。在HepG2细胞中,我们发现Chop表达以FXR/视黄酸X受体(RXR)依赖的方式受到调控。我们在人类CHOP启动子中鉴定出一个FXR/RXR结合位点,证明了一条高度保守的调控途径。我们的研究表明,在脂肪性肝炎小鼠模型中FXR/RXR调节Chop表达,为该疾病的发病机制提供了新的见解。