Hepatitis C virus core protein compromises iron-induced activation of antioxidants in mice and HepG2 cells

✍ Scribed by Kyoji Moriya; Hideyuki Miyoshi; Seiko Shinzawa; Takeya Tsutsumi; Hajime Fujie; Koji Goto; Yoshizumi Shintani; Hiroshi Yotsuyanagi; Kazuhiko Koike

• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 204 KB
• Volume: 82
• Category: Article
• ISSN: 0146-6615
• DOI: 10.1002/jmv.21661

✦ Synopsis

Abstract

One of the characteristics of hepatitis C virus (HCV) infection is the unusual augmentation of oxidative stress, which is exacerbated by iron accumulation in the liver, as observed frequently in hepatitis C patients. Using a transgenic mouse model, the core protein of HCV was shown previously to induce the overproduction of reactive oxygen species (ROS) in the liver. In the present study, the impact of iron overloading on the oxidant/antioxidant system was examined using this mouse model and cultured cells. Iron overloading caused the induction of ROS as well as antioxidants. However, the augmentation of some antioxidants, including heme oxygenase‐1 and NADH dehydrogenase, quinone 1, was compromised by the presence of the core protein. The attenuation of iron‐induced augmentation of heme oxygenase‐1 was also confirmed in HepG2 cells expressing the core protein. This attenuation was not dependent on the Nrf2 transcription factor. Thus, HCV infection not only induces oxidative stress but also hampers the iron‐induced antioxidant activation in the liver, thereby exacerbating oxidative stress that would facilitate hepatocarcinogenesis. J. Med. Virol. 82: 776–782, 2010. © 2010 Wiley‐Liss, Inc.