Gene expression profiling of dexamethasone-treated RBL-2H3 cells: induction of anti-inflammatory molecules

Immunol Lett. 2005 May 15;98(2):272-9. doi: 10.1016/j.imlet.2004.12.009. Epub 2005 Jan 5.

Abstract

Glucocorticoids are well known for their anti-inflammatory effect through the regulation of gene expression in many types of immune cells, including mast cells. However, the genes that are involved in suppression of mast cell-mediated inflammation by glucocorticoids have not been fully identified. Therefore, we examined the dexamethasone (Dex)-responsive genes in RBL-2H3 mast cells using a high-density oligonucleotide microarray technique. Gene expression profiling revealed that the antigen-induced up-regulation of pro-inflammatory factors, including monocyte chemoattractant protein-1, was markedly inhibited by 100 nM Dex. On the other hand, Dex treatment itself caused the substantial up-regulation of many genes, including phenylethanolamine-N-methyl transferase (PNMT) and cytokine-inducible SH2-containing protein (CISH), in the mast cells. The expression of these two genes significantly increased 6 h after Dex exposure and lasted for more than 24 h. Considering that PNMT is the rate-determining enzyme in epinephrine synthesis and that CISH is a suppressor of cytokine signaling, these Dex-responsive genes may be potential anti-inflammatory factors. Thus, gene expression profiling suggested that Dex might exert its anti-inflammatory effect through two pathways in mast cells: the suppression and induction of potentially pro- and anti-inflammatory factors, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / metabolism*
  • Antigens / immunology
  • Calcium Signaling / drug effects
  • Cell Degranulation / drug effects
  • Cell Line, Tumor
  • Chemokine CCL2 / metabolism
  • Dexamethasone / pharmacology*
  • Gene Expression Profiling*
  • Gene Expression Regulation / drug effects*
  • Immediate-Early Proteins / genetics
  • Inflammation / immunology
  • Inflammation / metabolism
  • Phenylethanolamine N-Methyltransferase / genetics
  • Phenylethanolamine N-Methyltransferase / metabolism
  • RNA, Messenger / genetics
  • Rats
  • Suppressor of Cytokine Signaling Proteins

Substances

  • Anti-Inflammatory Agents
  • Antigens
  • Ccl2 protein, rat
  • Chemokine CCL2
  • Immediate-Early Proteins
  • RNA, Messenger
  • Suppressor of Cytokine Signaling Proteins
  • cytokine inducible SH2-containing protein
  • Dexamethasone
  • Phenylethanolamine N-Methyltransferase