Abdalla Maher Y, Ahmad Iman M, Spitz Douglas R, Schmidt Warren N, Britigan Bradley E
Department of Internal Medicine of the Roy G. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
J Med Virol. 2005 Aug;76(4):489-97. doi: 10.1002/jmv.20388.
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-DCFH(2)) 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.
慢性丙型肝炎病毒(HCV)感染会导致肝脏氧化应激增加。肝脏抗氧化酶是抵御氧化损伤的重要防线。为了解肝细胞对不同HCV蛋白的抗氧化反应,我们比较了表达HCV核心蛋白和HCV非结构蛋白的肝细胞系中抗氧化酶的变化。我们发现,通过氧化敏感探针5-(及-6)-氯甲基-2',7'-二氯二氢荧光素二乙酸酯(CM-DCFH₂)荧光增强、还原型谷胱甘肽(GSH)减少以及硫氧还蛋白(Trx)氧化增加来确定,肝细胞系中HCV核心蛋白的表达会导致氧化应激增加。虽然HCV非结构(HCV-NS)蛋白的表达也会导致氧化应激增加,但抗氧化酶反应不同。HCV-NS蛋白的过表达会增加抗氧化酶(锰超氧化物歧化酶和过氧化氢酶)、血红素加氧酶-1(HO-1)和GSH,表明其促氧化活性机制与HCV核心蛋白不同。我们的研究结果表明,不同的HCV蛋白在肝细胞中诱导不同的抗氧化防御反应。这些发现可能有助于理解不同HCV蛋白与受感染肝细胞的相互作用,并有助于确定在HCV感染期间可能导致肝细胞损伤的因素。