CYLD regulates HGF expression in hepatic stellate cells via interaction with HDAC7.
Research output: Contribution to journal › Article
Hepatic fibrosis is considered as a physiological wound-healing response to liver injury. The process involves several factors, such as the hepatocyte growth factor (HGF), which restrain hepatic injury and facilitate the reversibility of the fibrotic reaction in response to an acute insult. Chronic liver injury and sustained inflammation cause progressive fibrosis and, ultimately, organ dysfunction. The mechanisms tipping the balance from restoration to progressive liver tissue scarring are not well understood. In the present study, we identify a mechanism in which the tumor suppressor gene, cylindromatosis (CYLD), confers protection from hepatocellular injury and fibrosis. Mice lacking CYLD (CYLD(-/-) ) were highly susceptible to hepatocellular damage, inflammation and fibrosis and revealed significantly lower hepatic HGF-levels compared with wild-type animals. Exogenous application of HGF rescued the liver injury phenotype of CYLD(-/-) mice. In the absence of CYLD, gene transcription of HGF in hepatic stellate cells was repressed through the binding of histone deacetylase 7 (HDAC7) to the promoter of HGF. In wildtype cells, CYLD removed HDAC7 from HGF promoter and induced HGF expression. Noteworthy, this interaction occurred independent of deubiquitinating activity of CYLD. Conclusions: Our findings highlight a novel link between CYLD and HDAC7, offering mechanistic insight into the contribution of these proteins to the progression of liver disease. Thus, through the regulation of the HGF level, CYLD ameliorates hepatocellular damage and liver fibrogenesis. (Hepatology 2014).
|Research areas and keywords||
Subject classification (UKÄ) – MANDATORY
|Publication status||Published - 2014|