Cyclooxygenase-2/prostaglandin D2/CRTH2 pathway mediates double-stranded RNA-induced enhancement of allergic airway inflammation

J Immunol. 2008 Jan 1;180(1):541-9. doi: 10.4049/jimmunol.180.1.541.

Abstract

Respiratory RNA viruses responsible for the common cold often worsen airway inflammation and bronchial responsiveness, two characteristic features of human asthma. We studied the effects of dsRNA, a nucleotide synthesized during viral replication, on airway inflammation and bronchial hyperresponsiveness in murine models of asthma. Intratracheal instillation of poly I:C, a synthetic dsRNA, increased the airway eosinophilia and enhanced bronchial hyperresponsiveness to methacholine in OVA-sensitized, exposed rats. These changes were associated with induction of cyclooxygenase-2 (COX-2) expression and COX-2-dependent PGD2 synthesis in the lungs, particularly in alveolar macrophages. The direct intratracheal instillation of PGD2 enhanced the eosinophilic inflammation in OVA-exposed animals, whereas pretreatment with a dual antagonist against the PGD2 receptor-(CRTH2) and the thromboxane A2 receptor, but not with a thromboxane A2 receptor-specific antagonist, nearly completely eliminated the dsRNA-induced worsening of airway inflammation and bronchial hyperresponsiveness. CRTH2-deficient mice had the same degree of allergen-induced airway eosinophilia as wild-type mice, but they did not exhibit a dsRNA-induced increase in eosinophil accumulation. Our data demonstrate that COX-2-dependent production of PGD2 followed by eosinophil recruitment into the airways via a CRTH2 receptor are the major pathogenetic factors responsible for the dsRNA-induced enhancement of airway inflammation and responsiveness.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cyclooxygenase 2 / metabolism*
  • Eosinophils / immunology
  • Macrophages, Alveolar / immunology
  • Mice
  • Mice, Mutant Strains
  • Poly I-C / immunology
  • Prostaglandin D2 / metabolism*
  • RNA, Double-Stranded / immunology*
  • Rats
  • Rats, Inbred Strains
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / metabolism*
  • Receptors, Prostaglandin / genetics
  • Receptors, Prostaglandin / metabolism*
  • Respiratory Hypersensitivity / immunology*
  • Respiratory Hypersensitivity / pathology

Substances

  • RNA, Double-Stranded
  • Receptors, Immunologic
  • Receptors, Prostaglandin
  • Cyclooxygenase 2
  • Ptgs2 protein, rat
  • Poly I-C
  • Prostaglandin D2
  • prostaglandin D2 receptor