Down-regulation of heme oxygenase-1 by hepatitis C virus infection in vivo and by the in vitro expression of hepatitis C core protein

J Infect Dis. 2004 Sep 15;190(6):1109-18. doi: 10.1086/423488. Epub 2004 Aug 17.

Abstract

Antioxidant enzymes, including heme oxygenase (HO)-1, are an important line of defense against oxidant-mediated liver injury. Because hepatitis C virus (HCV) infection appears to increase the production of oxidants, we evaluated levels of antioxidant enzymes and HO-1 in liver-biopsy samples from HCV-infected patients by immunoblot and semiquantitative reverse-transcriptase polymerase chain reaction. In HCV-infected liver samples, levels of immunoreactive HO-1 and HO-1 mRNA were >4-fold lower than levels in control samples, but levels of superoxide dismutase and catalase were unaffected. Immunohistochemical results confirmed the decreased expression of HO-1 in hepatocytes from liver samples from HCV-infected patients but not in those from patients with other chronic liver diseases. The expression of HO-1 was also reduced in cell lines that stably express HCV core protein, which suggests that core gene products are capable of regulating the expression of HO-1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Biopsy
  • Blotting, Western
  • Catalase / analysis
  • Cell Line
  • Down-Regulation / genetics
  • Down-Regulation / physiology*
  • Heme Oxygenase (Decyclizing) / analysis*
  • Heme Oxygenase (Decyclizing) / genetics
  • Heme Oxygenase (Decyclizing) / immunology
  • Heme Oxygenase-1
  • Hepacivirus / metabolism
  • Hepacivirus / pathogenicity*
  • Humans
  • Immunohistochemistry
  • Liver / enzymology
  • Liver / pathology
  • Membrane Proteins
  • RNA / analysis
  • RNA / isolation & purification
  • RNA, Messenger / analysis
  • RNA, Messenger / isolation & purification
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superoxide Dismutase / analysis
  • Viral Core Proteins / metabolism*

Substances

  • Membrane Proteins
  • RNA, Messenger
  • Viral Core Proteins
  • nucleocapsid protein, Hepatitis C virus
  • RNA
  • Catalase
  • HMOX1 protein, human
  • Heme Oxygenase (Decyclizing)
  • Heme Oxygenase-1
  • Superoxide Dismutase