Hepatitis C virus core protein does not inhibit apoptosis in human hepatoma cells

Eur J Clin Invest. 1999 Nov;29(11):940-6. doi: 10.1046/j.1365-2362.1999.00559.x.

Abstract

Background: Viral persistence is a major problem after infection with the hepatitis C virus. Recently, it has been reported that hepatitis C virus core protein inhibits cis-platin induced apoptosis in human cervical carcinoma cells and apoptosis induced by overexpression of c-myc in Chinese hamster ovary cells.

Materials and methods: This study investigated whether different variants of hepatitis C virus core or E2 protein interfere with tumour necrosis factor alpha or Fas (CD95/ APO-1) antibody-induced programmed cell death in transiently transfected human hepatoma (HepG2) cells.

Results: While neither full length or C-terminally truncated variants of hepatitis C virus core protein nor hepatitis C virus E2 protein inhibited tumour necrosis factor alpha- or Fas antibody-induced apoptosis, a strong inhibition was observed with the cowpox virus cytokine response modifier A protein.

Conclusions: Thus, it is unlikely that hepatitis C virus core or E2 protein inhibit apoptosis mediated by apoptosis-signalling pathways sensitive to cytokine response modifier A protein. Discrepancies to previous reports probably reflect specific effects of hepatitis C virus core protein on different apoptotic pathways and/ or cell lines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • CHO Cells
  • Carcinoma, Hepatocellular
  • Cricetinae
  • Cycloheximide / pharmacology
  • Fluorescent Antibody Technique, Indirect
  • Genes, myc
  • Hepacivirus / genetics*
  • Humans
  • Liver Neoplasms
  • Recombinant Proteins / metabolism
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology
  • Viral Core Proteins / genetics
  • Viral Core Proteins / physiology*
  • fas Receptor / analysis
  • fas Receptor / biosynthesis

Substances

  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Viral Core Proteins
  • fas Receptor
  • nucleocapsid protein, Hepatitis C virus
  • Cycloheximide