Respiratory syncytial virus infection activates STAT signaling in human epithelial cells

Biochem Biophys Res Commun. 2003 Jun 27;306(2):616-22. doi: 10.1016/s0006-291x(03)01008-8.

Abstract

Acute respiratory syncytial virus (RSV) infection causes airway inflammation and exacerbates asthma, but the mechanism of inflammation is poorly understood. The role of the STAT-signaling pathway in RSV infection in epithelial cells was examined in this study. DNA microarray analyses of RSV-infected human alveolar type II (A549) epithelial cells identified several genes whose expression was altered from -5.5 to +56.4-fold. Four of the highly expressed genes contained STAT-binding elements. In A549 and normal human bronchial epithelial cells (NHBE), RSV induced phosphorylation and nuclear translocation of STAT-1alpha that was abrogated when RSV attachment was blocked. Treatment with a JAK-2 inhibitor or transfection with dominant-negative STAT-1alpha blocked STAT-1alpha activation and RSV infection. RSV also activated STAT-3 and IL-6 specific antibodies blocked this activation. Thus, activation of the STAT-1alpha and STAT-3 pathways play a role in RSV infection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Active Transport, Cell Nucleus
  • Cell Line
  • DNA / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Epithelial Cells / metabolism*
  • Genes, Reporter
  • Heparin / metabolism
  • Heparin Lyase / metabolism
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Interferon-Stimulated Gene Factor 3
  • Interleukin-6 / metabolism
  • Microscopy, Fluorescence
  • Models, Genetic
  • Oligonucleotide Array Sequence Analysis
  • Phosphorylation
  • Promoter Regions, Genetic
  • RNA, Messenger / metabolism
  • Respiratory Syncytial Virus Infections / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction*
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Interferon-Stimulated Gene Factor 3
  • Interleukin-6
  • RNA, Messenger
  • Transcription Factors
  • gamma interferon activation factor
  • Heparin
  • DNA
  • Heparin Lyase