Activated macrophages promote hepatitis C virus entry in a tumor necrosis factor-dependent manner

Hepatology. 2014 Apr;59(4):1320-30. doi: 10.1002/hep.26911. Epub 2014 Feb 25.

Abstract

Macrophages are critical components of the innate immune response in the liver. Chronic hepatitis C is associated with immune infiltration and the infected liver shows a significant increase in total macrophage numbers; however, their role in the viral life cycle is poorly understood. Activation of blood-derived and intrahepatic macrophages with a panel of Toll-like receptor agonists induce soluble mediators that promote hepatitis C virus (HCV) entry into polarized hepatoma cells. We identified tumor necrosis factor α (TNF-α) as the major cytokine involved in this process. Importantly, this effect was not limited to HCV; TNF-α increased the permissivity of hepatoma cells to infection by Lassa, measles and vesicular stomatitis pseudoviruses. TNF-α induced a relocalization of tight junction protein occludin and increased the lateral diffusion speed of HCV receptor tetraspanin CD81 in polarized HepG2 cells, providing a mechanism for their increased permissivity to support HCV entry. High concentrations of HCV particles could stimulate macrophages to express TNF-α, providing a direct mechanism for the virus to promote infection.

Conclusion: This study shows a new role for TNF-α to increase virus entry and highlights the potential for HCV to exploit existing innate immune responses in the liver to promote de novo infection events.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / virology*
  • Cell Line, Tumor
  • Cell Polarity / physiology
  • Hep G2 Cells
  • Hepacivirus / physiology*
  • Hepatitis C / metabolism
  • Hepatitis C / physiopathology
  • Humans
  • Immunity, Innate / physiology
  • Interleukin-1beta / physiology
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology
  • Liver Neoplasms / virology*
  • Macrophage Activation / physiology*
  • Macrophages / physiology*
  • Occludin / metabolism
  • Tetraspanin 28 / metabolism
  • Tight Junctions / physiology
  • Tumor Necrosis Factor-alpha / physiology*
  • Virus Internalization*

Substances

  • Interleukin-1beta
  • Occludin
  • Tetraspanin 28
  • Tumor Necrosis Factor-alpha