Regulation of mast cell signaling through high-affinity IgE receptor by CD45 protein tyrosine phosphatase

Int Immunol. 2000 Feb;12(2):169-76. doi: 10.1093/intimm/12.2.169.

Abstract

The transmembrane tyrosine phosphatase CD45 regulates the activity of src family protein tyrosine kinases (PTK) and thereby influences the signaling via such receptors as T and B cell antigen receptors associated with these PTK. However, its implication in signaling through the mast cell receptor with high affinity for IgE (FcepsilonRI) is less clear, although Lyn, a member of the src family, plays an important role in FcepsilonRI-mediated signaling. To define a role for CD45 in FcepsilonRI signal transduction, we established CD45 high expressing rat basophilic leukemia cell lines (RBL-CD45H) and cell lines expressing trace amounts of CD45 (RBL-CD45L). We demonstrate that although all RBL-CD45L cell lines degranulate following IgE- and antigen-induced FcepsilonRI aggregation, the response is significantly reduced at a low dose of antigen. The cells show a delayed and slowed Ca(2+) mobilization even though at a higher dose where the cells degranulate to a similar extent as RBL-CD45H. This diminished Ca(2+) response is restored by reconstitution of RBL-CD45L with a chimeric molecule containing the cytoplasmic phosphatase domains of rat CD45. Furthermore, tyrosine phosphorylation of FcepsilonRI, association of FcepsilonRI with Lyn and PTK activity associated with FcepsilonRI, all of which are enhanced upon FcepsilonRI aggregation in RBL-CD45H, are impaired in RBL-CD45L. Finally, we show that FcepsilonRI is physically associated with CD45 in RBL-CD45H prior to receptor aggregation. Thus, we propose that, although not indispensable in mast cell degranulation, CD45 positively regulates the signaling through FcepsilonRI by promoting the activation of FcepsilonRI-associated Lyn.

MeSH terms

  • Animals
  • Calcium / metabolism
  • Flow Cytometry
  • Gene Expression Regulation
  • Leukemia, Basophilic, Acute
  • Leukocyte Common Antigens / metabolism*
  • Mast Cells / immunology
  • Mast Cells / physiology*
  • Phosphorylation
  • Rats
  • Receptors, IgE / genetics
  • Receptors, IgE / metabolism*
  • Signal Transduction*
  • Tumor Cells, Cultured
  • Tyrosine / metabolism
  • src-Family Kinases / metabolism

Substances

  • Receptors, IgE
  • Tyrosine
  • src-Family Kinases
  • Leukocyte Common Antigens
  • Calcium