LTA and LPS mediated activation of protein kinases in the regulation of inflammatory cytokines expression in macrophages

Clin Chim Acta. 2006 Dec;374(1-2):106-15. doi: 10.1016/j.cca.2006.05.045. Epub 2006 Jun 10.

Abstract

Background: Lipoteichoic acid (LTA) and lipopolysaccharide (LPS), the toxicants from bacteria, are potent inducers of inflammatory cytokines, such as tumor necrosis factor-alpha (TNF) and interleukin-1beta (IL-1). Although LTA is much less reported than that on LPS, LTA is regarded as the gram-positive equivalent to LPS in some aspects. We investigated the LTA-induced signal transduction and biological effects, as well as to compare the effect of LTA with that of LPS.

Methods: Kinase assay, ELISA and RT-PCR were performed to delineate LTA and LPS signaling as well as to determine the secretion and RNA expression of TNF and IL-1.

Results: Src, Lyn and MAPKs are involved in LTA and LPS signaling in murine macrophages. Additionally, blockades of PKC, PI3K and p38, respectively, caused significant inhibition of both LTA- and LPS-induced proIL-1/IL-1 and TNF expression. ERK inactivation moderately reduced LTA- and LPS-induced proIL-1/IL-1, but considerably reduced TNF expression. Inhibition of JNK engendered super-induction of IL-1 secretion, but diminished TNF secretion. Strikingly, both IL-1 and TNF protein induction were declined by overexpression of dominant negative form of JNK.

Conclusions: The results clarify the similarity and difference between LTA- and LPS-mediated signal transduction and induction of inflammatory cytokines in macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cells, Cultured
  • Escherichia / immunology
  • Interleukin-1 / metabolism*
  • Lipopolysaccharides / pharmacology*
  • Macrophages / immunology*
  • Mice
  • Polysaccharides, Bacterial / pharmacology*
  • Protein Kinases / drug effects
  • Protein Kinases / metabolism*
  • Signal Transduction / drug effects
  • Streptococcaceae / immunology
  • Teichoic Acids / pharmacology*
  • Tumor Necrosis Factor-alpha / metabolism*
  • Up-Regulation

Substances

  • Interleukin-1
  • Lipopolysaccharides
  • Polysaccharides, Bacterial
  • Teichoic Acids
  • Tumor Necrosis Factor-alpha
  • lipoteichoic acid
  • Protein Kinases