Phosphotidylinositol-3 kinase-mediated signals in mice immunized with the 57 kDa major antigenic outer-membrane protein of Shigella dysenteriae type 1

J Med Microbiol. 2005 Jul;54(Pt 7):631-637. doi: 10.1099/jmm.0.46014-0.

Abstract

Antigen-specific T-cell signalling via T-cell antigen receptor stimulation was carried out in BALB/c mice immunized with the 57 kDa major antigenic component of Shigella dysenteriae 1 outer-membrane proteins. In presence of anti-CD3, the 57 kDa antigen was found to increase the level of IL-2 significantly instead of IL-4. IL-2 production in T cells was consistent with an increase in intracellular free Ca(2+) [(Ca(2+))i] concentration. The antigen-specific modulation was observed during T-cell signalling, with enhanced release of [(Ca(2+))i]. IL-2-receptor stimulation via IL-2 did not significantly induce the release of IL-2 with consistent intracellular Ca(2+) production. Furthermore, the protein tyrosine kinase was activated during anti-CD3 stimulation, which up-regulated the phosphatidylinositol kinase of p85-mediated serine kinase protein kinase-C of p70. Phosphoinositide-specific kinases are regulated by the phosphorylation of tyrosine kinase through the activation of the T-cell antigen receptor. The above findings indicate that phosphotidylinositol-3 kinase-mediated signals are up-regulated through [(Ca(2+))i], which is essential for Th1-type responses.

MeSH terms

  • Animals
  • Antigens, Bacterial / immunology*
  • Bacterial Outer Membrane Proteins / immunology*
  • Blotting, Western
  • CD3 Complex / immunology
  • Calcium / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Inhibitors / pharmacology
  • Immunoprecipitation
  • Interleukin-2 / biosynthesis
  • Interleukin-4 / biosynthesis
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoinositide-3 Kinase Inhibitors
  • Phosphorylation
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism
  • Receptors, Antigen, T-Cell / physiology
  • Shigella dysenteriae / immunology*
  • Signal Transduction / physiology
  • Sirolimus / pharmacology
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / immunology*
  • Up-Regulation / physiology

Substances

  • Antigens, Bacterial
  • Bacterial Outer Membrane Proteins
  • CD3 Complex
  • Enzyme Inhibitors
  • Interleukin-2
  • Phosphoinositide-3 Kinase Inhibitors
  • Receptors, Antigen, T-Cell
  • Interleukin-4
  • Protein Kinase C
  • Calcium
  • Sirolimus