The vesicular stomatitis virus matrix protein inhibits glycoprotein 130-dependent STAT activation

J Immunol. 2001 Nov 1;167(9):5209-16. doi: 10.4049/jimmunol.167.9.5209.

Abstract

Infection of cells by vesicular stomatitis virus (VSV) results in the inhibition of host transcription. We show in this study that infection of HeLa cells with VSV leads to a strongly diminished activation of STAT3 and STAT1 by the inflammatory cytokine IL-6. This effect was mimicked by forced expression of a single viral protein, the matrix (M)-protein of VSV, which blocked STAT activation via chimeric receptors containing the cytoplasmic domain of the IL-6 signal transducer gp130. Western blot analysis revealed that VSV M-protein did not inhibit the nuclear translocation of activated STAT3 but did inhibit its tyrosine phosphorylation. Inhibition of STAT activation was not dependent on tyrosine 759 of the IL-6 signal transducer gp130, suggesting that the inhibitory action of VSV M-protein is not mediated by the induction of the suppressor of cytokine signaling 3. VSV M-protein inhibited gene transcription from cotransfected alpha(2)-macroglobulin or antichymotrypsin promoter/luciferase reporter constructs which contain STAT3-binding sites. However, transcription from a STAT5-dependent construct was not negatively affected. In conclusion, our data suggest that infection by VSV and specifically overexpression of the viral M-protein interferes with an important signaling pathway necessary for triggering antiviral and inflammatory responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / physiology*
  • Cytokine Receptor gp130
  • DNA-Binding Proteins / physiology*
  • HeLa Cells
  • Humans
  • Interleukin-6 / pharmacology
  • JNK Mitogen-Activated Protein Kinases*
  • MAP Kinase Kinase 4
  • Membrane Glycoproteins / physiology*
  • Mitogen-Activated Protein Kinase Kinases / physiology
  • Phosphorylation
  • STAT3 Transcription Factor
  • Trans-Activators / physiology*
  • Transcription, Genetic
  • Tyrosine / metabolism
  • Vesicular stomatitis Indiana virus / pathogenicity*
  • Viral Matrix Proteins / toxicity*

Substances

  • Antigens, CD
  • DNA-Binding Proteins
  • IL6ST protein, human
  • Interleukin-6
  • Membrane Glycoproteins
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Trans-Activators
  • Viral Matrix Proteins
  • Cytokine Receptor gp130
  • Tyrosine
  • JNK Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4
  • Mitogen-Activated Protein Kinase Kinases