Hepatitis C virus‐core and non structural proteins lead to different effects on cellular antioxidant defenses
- 23 June 2005
- journal article
- research article
- Published by Wiley in Journal of Medical Virology
- Vol. 76 (4) , 489-497
- https://doi.org/10.1002/jmv.20388
Abstract
Chronic hepatitis C virus (HCV) infection leads to increased oxidative stress in the liver. Hepatic antioxidant enzymes provide an important line of defense against oxidative injury. To understand the antioxidant responses of hepatocytes to different HCV proteins, we compared changes in antioxidative enzymes in HCV-core and HCV-nonstructural protein expressing hepatocyte cell lines. We found that expression of HCV-core protein in hepatocyte cell lines leads to increased oxidative stress as determined by increased in the oxidant-sensitive probe 5-(and-6)-chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate (CM-DCFH2) fluorescence, decreased reduced glutathione (GSH), and increased oxidation of thioredoxin (Trx). Although the expression of HCV-nonstructural (HCV-NS) proteins led to increased oxidative stress as well, the antioxidant enzymatic responses were different. Over-expression of HCV-NS proteins increased antioxidant enzymes (MnSOD and catalase), heme oxygenase-1 (HO-1), and GSH, indicating different mechanism(s) of prooxidative activity than HCV-core protein. Our findings show that different HCV proteins induce different antioxidant defense responses in hepatocytes. These findings may facilitate understanding the interaction of different HCV proteins with infected liver cells and help identify possible factors contributing to hepatocyte damage during HCV infection. J. Med. Virol. 76:489–497, 2005.Keywords
This publication has 45 references indexed in Scilit:
- Expression of Gastrointestinal Glutathione Peroxidase Is Inversely Correlated to the Presence of Hepatitis C Virus Subgenomic RNA in Human Liver CellsJournal of Biological Chemistry, 2005
- Down‐Regulation of Heme Oxygenase–1 by Hepatitis C Virus Infection In Vivo and by the In Vitro Expression of Hepatitis C Core ProteinThe Journal of Infectious Diseases, 2004
- Induced oxidative stress and activated expression of manganese superoxide dismutase during hepatitis C virus replication: role of JNK, p38 MAPK and AP-1Biochemical Journal, 2004
- Increased prooxidant production and enhanced susceptibility to glutathione depletion in HepG2 cells co‐expressing HCV core protein and CYP2E1Journal of Medical Virology, 2003
- Redox Potential of Human Thioredoxin 1 and Identification of a Second Dithiol/Disulfide MotifJournal of Biological Chemistry, 2003
- Cellular response to conditional expression of hepatitis C virus core protein in Huh7 cultured human hepatoma cellsHepatology, 2002
- Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell LineScience, 1999
- Superoxide Dismutase in Patients With Chronic Hepatitis C Virus InfectionFree Radical Biology & Medicine, 1998
- Natural history of hepatitis CHepatology, 1997
- In situ detection of lipid peroxidation in chronic hepatitis C: correlation with pathological features.Journal of Clinical Pathology, 1997