HCV NS5A inhibits interferon-alpha signaling through suppression of STAT1 phosphorylation in hepatocyte-derived cell lines

J Hepatol. 2007 May;46(5):759-67. doi: 10.1016/j.jhep.2006.11.013. Epub 2006 Dec 14.

Abstract

Background/aims: HCV NS5A appears to play an important role in HCV resistance to IFN-alpha but the molecular mechanism is not fully elucidated. Most studies regarding the involvement of signal transducer and activator of transcription 1 (STAT1) in inhibition of IFN-alpha signaling by NS5A were performed in non-hepatic cell lines and their relevance may be debatable.

Methods: We analyzed the effects of NS5A on IFN-alpha signaling through STAT1 phosphorylation in three hepatocyte-derived cell lines, Hep3B, J5 and Huh7. Interaction of NS5A and STAT1 was also investigated with co-immunoprecipitation and confocal microscopy.

Results: IFN-alpha induces STAT1 activation in Hep3B cells in a dose- and time-dependent manner. Transient or stable NS5A expression inhibits STAT1 phosphorylation in a dose-dependent manner in hepatocyte-derived cell lines, whereas the levels of STAT1 phosphorylation remain unchanged in non-hepatocyte HeLa and COS7 cells despite increasing amounts of NS5A. The NS5A may interact with STAT1, specifically, the N-terminal 488 amino acids of STAT1. Furthermore, NS5A inhibits activation of interferon-stimulated gene factor 3 (ISGF3) and interferon-stimulated response element (ISRE)-driven gene expression, as demonstrated by electrophoretic mobility shift assay and luciferase assay, respectively.

Conclusions: NS5A may interact with STAT1 and inhibit IFN-alpha signaling through suppression of STAT1 phosphorylation specifically in hepatocyte-derived cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation, Enzymologic
  • HeLa Cells
  • Hepacivirus / metabolism*
  • Hepatocytes / enzymology
  • Hepatocytes / virology*
  • Humans
  • Immunohistochemistry
  • Immunoprecipitation
  • Interferon-alpha / antagonists & inhibitors
  • Interferon-alpha / metabolism*
  • Microscopy, Confocal
  • Phosphorylation
  • Protein-Tyrosine Kinases / metabolism
  • STAT1 Transcription Factor / metabolism*
  • Signal Transduction*
  • Trans-Activators / metabolism*
  • Transcriptional Activation
  • Transfection
  • Viral Nonstructural Proteins / metabolism*

Substances

  • Interferon-alpha
  • STAT1 Transcription Factor
  • Trans-Activators
  • Viral Nonstructural Proteins
  • Protein-Tyrosine Kinases
  • NS-5 protein, hepatitis C virus