Characterization of gene expression in resting and activated mast cells

J Exp Med. 1998 Nov 2;188(9):1657-68. doi: 10.1084/jem.188.9.1657.

Abstract

To characterize gene expression in activated mast cells more comprehensively than heretofore, we surveyed the changes in genetic transcripts by the method of serial analysis of gene expression in the RBL-2H3 line of rat mast cells before and after they were stimulated through their receptors with high affinity for immunoglobulin E (FcepsilonRI). A total of 40,759 transcripts derived from 11,300 genes were analyzed. Among the diverse genes that had not been previously associated with mast cells and that were constitutively expressed were those for the cytokine macrophage migration inhibitory factor neurohormone receptors such as growth hormone- releasing factor and melatonin and components of the exocytotic machinery. In addition, several dozen transcripts were differentially expressed in response to antigen-induced clustering of the FcepsilonRI. Included among these were the genes for preprorelaxin, mitogen-activated protein kinase kinase 3, and the dual specificity protein phosphatase, rVH6. Significantly, the majority of genes differentially expressed in this well-studied model of mast cell activation have not been identified before this analysis.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Differentiation
  • DNA Primers / genetics
  • Gene Expression*
  • In Vitro Techniques
  • Mast Cells / cytology
  • Mast Cells / immunology*
  • Mast Cells / metabolism*
  • Mitogen-Activated Protein Kinase Kinases
  • Protein Kinases / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptor Aggregation
  • Receptors, IgE / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction

Substances

  • DNA Primers
  • RNA, Messenger
  • Receptors, IgE
  • Protein Kinases
  • Mitogen-Activated Protein Kinase Kinases