Cel
Over 3% of the world population is chronically infected by the hepatitis C virus (HCV). Chronic infection is associated with liver disease that leads to fibrosis and cirrhosis and ultimately to hepatocellular carcinoma (HCC). There is no vaccine for HCV and the current treatment is only partially effective and toxic. Consequently, HCV infection is one of the leading causes of liver transplantation worldwide. HCV depends heavily on cellular lipid and lipoprotein metabolism to replicate and produce infectious particles. This dependence coincides with the fact that chronic HCV infection is associated with alterations of the liver lipid metabolism. These alterations are manifested by abnormal accumulation of lipids in hepatocytes (steatosis) in a significant proportion of the patients. In patients responding to interferon treatment, steatosis subsides as the viral titers decrease, suggesting that HCV replication and viral protein expression are a major determinant for these alterations. However, little is known about the molecular mechanisms underlying the interference of HCV infection with lipid metabolism. Understanding how HCV exploits the cellular lipid and lipoprotein biosynthetic machinery might contribute to understanding important aspects of the pathogenesis of chronic HCV infection. In this application, we propose to use a cell culture HCV infection model that we recently developed to study the intersection of cellular lipid and lipoprotein metabolism with basic aspects of HCV infection.
Dziedzina nauki
Zaproszenie do składania wniosków
FP7-PEOPLE-2011-CIG
Zobacz inne projekty w ramach tego zaproszenia
System finansowania
MC-CIG - Support for training and career development of researcher (CIG)Koordynator
28006 Madrid
Hiszpania