Critical role of PA28[gamma] in hepatitis C virus-associated steatogenesis and hepatocarcinogenesis

Hepatitis C virus (HCV) is a major cause of chronic liver disease that frequently leads to steatosis, cirrhosis, and eventually hepatocellular carcinoma (HCC). HCV core protein is not only a component of viral particles but also a multifunctional protein because liver steatosis and HCC are developed in HCV core gene-transgenic (CoreTg) mice. Proteasome activator PA28[gamma],/REG[gamma] regulates host and viral proteins such as nuclear hormone receptors and HCV core protein. Here we show that a knockout of the PA28[gamma] gene induces the accumulation of HCV core protein in the nucleus of hepatocytes of CoreTg mice and disrupts development of both hepatic steatosis and HCC. Furthermore, the genes related to fatty acid biosynthesis and srebp-1c promoter activity were up-regulated by HCV core protein in the cell line and the mouse liver in a PA28[gamma]-dependent manner. Heterodimer composed of liver X receptor [alpha] (LXR[gamma]) and retinoid X receptor [alpha] (RXR[alpha]) is known to up-regulate srebp-1c promoter activity. Our data also show that HCV core protein enhances the binding of LXR[alpha]/RXR[alpha] to LXR-response element in the presence but not the absence of PA28[gamma]. These findings suggest that PA28[gamma] plays a crucial role in the development of liver pathology induced by HCV infection. fatty acid | proteasome | sterol regulatory element-binding protein (SREBP) | RXR[alpha] | LXR[alpha]