Involvement of protein tyrosine kinase in Toll-like receptor 4-mediated NF-kappa B activation in human peripheral blood monocytes

Am J Physiol Lung Cell Mol Physiol. 2003 Apr;284(4):L607-13. doi: 10.1152/ajplung.00116.2002. Epub 2002 Dec 20.

Abstract

Bacterial lipopolysaccharide (LPS) is a powerful activator of the innate immune system. Exposure to LPS induces an inflammatory reaction in the lung mediated primarily by human blood monocytes and alveolar macrophages, which release an array of inflammatory chemokines and cytokines including IL-8, TNF-alpha, IL-1beta, and IL-6. The signaling mechanisms utilized by LPS to stimulate the release of cytokines and chemokines are still incompletely understood. Pretreatment with the protein tyrosine kinase-specific inhibitors genistein and herbimycin A effectively blocked LPS-induced NF-kappaB activation as well as IL-8 gene expression in human peripheral blood monocytes. However, when genistein was added 2 min after the addition of LPS, no inhibition was observed. Utilizing a coimmunoprecipitation assay, we further showed that LPS-stimulated tyrosine phosphorylation of Toll-like receptor 4 (TLR4) may be involved in downstream signaling events induced by LPS. These findings provide evidence that LPS-induced NF-kappaB activation and IL-8 gene expression use a signaling pathway requiring protein tyrosine kinase and that such regulation may occur through tyrosine phosphorylation of TLR4.

Publication types

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

MeSH terms

  • Drosophila Proteins*
  • Gene Expression / drug effects
  • Gene Expression / immunology
  • Humans
  • Interleukin-8 / genetics
  • Lipopolysaccharides / pharmacology
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism*
  • Monocytes / metabolism*
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Receptors, Cell Surface / immunology
  • Receptors, Cell Surface / metabolism*
  • Signal Transduction / immunology*
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Transcriptional Activation / drug effects
  • Transcriptional Activation / immunology
  • Tyrosine / metabolism

Substances

  • Drosophila Proteins
  • Interleukin-8
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • NF-kappa B
  • Receptors, Cell Surface
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Tyrosine