Hepatitis C virus infection sensitizes human hepatocytes to TRAIL-induced apoptosis in a caspase 9-dependent manner

J Immunol. 2008 Oct 1;181(7):4926-35. doi: 10.4049/jimmunol.181.7.4926.

Abstract

Apoptosis of infected cells represents a key host defense mechanism against viral infections. The impact of apoptosis on the elimination of hepatitis C virus (HCV)-infected cells is poorly understood. The TRAIL has been implicated in the death of liver cells in hepatitis-infected but not in normal liver cells. To determine the impact of TRAIL on apoptosis of virus-infected host cells, we studied TRAIL-induced apoptosis in a tissue culture model system for HCV infection. We demonstrated that HCV infection sensitizes primary human hepatocytes and Huh7.5 hepatoma cells to TRAIL induced apoptosis in a dose- and time-dependent manner. Mapping studies identified the HCV nonstructural proteins as key mediators of sensitization to TRAIL. Using a panel of inhibitors targeting different apoptosis pathways, we demonstrate that sensitization to TRAIL is caspase-9 dependent and mediated in part via the mitochondrial pathway. Sensitization of hepatocytes to TRAIL-induced apoptosis by HCV infection represents a novel antiviral host defense mechanism that may have important implications for the pathogenesis of HCV infection and may contribute to the elimination of virus-infected hepatocytes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / immunology*
  • Autocrine Communication / genetics
  • Autocrine Communication / immunology
  • Carcinoma, Hepatocellular / enzymology
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / virology
  • Caspase 9 / physiology*
  • Cell Line, Tumor
  • Cells, Cultured
  • Gene Deletion
  • Hepacivirus / genetics
  • Hepacivirus / immunology*
  • Hepatocytes / enzymology
  • Hepatocytes / immunology
  • Hepatocytes / pathology*
  • Hepatocytes / virology*
  • Humans
  • Liver Neoplasms / enzymology
  • Liver Neoplasms / immunology
  • Liver Neoplasms / pathology
  • Liver Neoplasms / virology
  • Mitochondria / enzymology
  • Mitochondria / genetics
  • TNF-Related Apoptosis-Inducing Ligand / physiology*
  • Viral Core Proteins / biosynthesis
  • Viral Core Proteins / genetics
  • Viral Envelope Proteins / biosynthesis
  • Viral Envelope Proteins / genetics
  • Viral Nonstructural Proteins / biosynthesis
  • Viral Nonstructural Proteins / genetics
  • Viral Structural Proteins / biosynthesis
  • Viral Structural Proteins / genetics

Substances

  • E1 protein, Hepatitis C virus
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • Viral Core Proteins
  • Viral Envelope Proteins
  • Viral Nonstructural Proteins
  • Viral Structural Proteins
  • NS-5 protein, hepatitis C virus
  • Caspase 9