Exposure of RBL-2H3 mast cells to Ag(+) induces cell degranulation and mediator release

Biochem Biophys Res Commun. 2001 May 11;283(3):707-14. doi: 10.1006/bbrc.2001.4844.

Abstract

There is a growing need to understand the impact of environmental sulfhydryl group-reactive heavy metals on the immune system. Here we show that Ag(+) induces mast cell degranulation, as does the aggregation of the high affinity immunoglobulin E receptor (FcepsilonRI). Micromolar quantities of Ag(+) specifically induced degranulation of mast cell model rat basophilic leukemia (RBL-2H3) cells without showing cytotoxicity. The Ag(+)-mediated degranulation could be observed as rapidly as 5 min after the addition of the ions. Ag(+) also induced a rapid change in tyrosine phosphorylation of multiple cellular proteins including the focal adhesion kinase but not Syk kinase. The Syk-selective inhibitor piceatannol and the Src family-selective tyrosine kinase inhibitor PP1 dose-dependently inhibited FcepsilonRI-mediated degranulation, whereas neither compound inhibited the Ag(+)-mediated degranulation. Furthermore, likewise FcepsilonRI aggregation, Ag(+) also induced leukotriene secretion. These results show that Ag(+) activates RBL-2H3 mast cells through a tyrosine phosphorylation-linked mechanism, which is distinct from that involved in FcepsilonRI-mediated activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Degranulation / drug effects
  • Cell Line
  • Enzyme Inhibitors / pharmacology
  • Enzyme Precursors / chemistry
  • Enzyme Precursors / metabolism
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Histamine Release / drug effects
  • Intracellular Signaling Peptides and Proteins
  • Leukotrienes / metabolism*
  • Mast Cells / drug effects*
  • Mast Cells / immunology
  • Mast Cells / physiology*
  • Mercury / toxicity
  • Phosphorylation
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / chemistry
  • Protein-Tyrosine Kinases / metabolism
  • Proteins / chemistry
  • Proteins / metabolism
  • Rats
  • Receptors, IgE / metabolism
  • Silver / toxicity*
  • Syk Kinase
  • Tyrosine / chemistry
  • Tyrosine / metabolism

Substances

  • Enzyme Inhibitors
  • Enzyme Precursors
  • Intracellular Signaling Peptides and Proteins
  • Leukotrienes
  • Proteins
  • Receptors, IgE
  • Silver
  • Tyrosine
  • Protein-Tyrosine Kinases
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Ptk2 protein, rat
  • Syk Kinase
  • Syk protein, rat
  • Mercury