Peroxisome proliferator-activated receptor-γ is expressed in eosinophils in nasal polyps

Int Arch Allergy Immunol. 2011:155 Suppl 1:57-63. doi: 10.1159/000327294. Epub 2011 Jun 1.

Abstract

Background: Peroxisome proliferator-activated receptor-γ (PPARγ) is a member of the nuclear receptors, which regulate fatty acid metabolites. One of the natural ligands for PPARγ is 15-deoxy-Δ(12,14)-prostaglandin J(2) (15d-PGJ(2)), a major metabolite of prostaglandin D(2) (PGD(2)). Recently, PPARγ has been shown to play an important role in anti-inflammatory reactions, including within-airway allergic diseases, in a mouse model. Our aim was to clarify the expression and localization of PPARγ and PGD(2) synthase, which produces ligands of PPARγ, in nasal polyps by immunohistochemical analysis.

Methods: Nasal polyps of chronic rhinosinusitis patients (6 asthmatic patients and 6 nonasthmatic patients) were obtained during surgery. May-Grünwald-Giemsa staining was performed to evaluate the eosinophil infiltration of the polyps. To identify the cells expressing PPARγ protein and PGD(2) synthase, double immunostaining was performed using anti-PPARγ antibody, monoclonal antileukocyte antibodies, and PGD(2) synthase antibody.

Results: The number of eosinophils and the number of PPARγ-positive cells in the nasal polyps of the asthmatic patients were significantly higher than those in the nonasthmatic patients. PPARγ was expressed on eosinophils and T cells of the infiltrating cells in the nasal polyps. PGD(2) synthase was also expressed on PPARγ-positive cells.

Conclusion: PPARγ is involved in nasal polyposis pathogenesis, acting on eosinophils and T cells.

MeSH terms

  • Asthma / complications
  • Asthma / pathology
  • Cell Count
  • Eosinophils / metabolism*
  • Eosinophils / pathology
  • Humans
  • Intramolecular Oxidoreductases / metabolism
  • Lipocalins / metabolism
  • Nasal Polyps / etiology
  • Nasal Polyps / metabolism
  • Nasal Polyps / pathology*
  • PPAR gamma / metabolism*
  • Rhinitis / complications
  • Rhinitis / pathology
  • Sinusitis / complications
  • Sinusitis / pathology
  • T-Lymphocytes / metabolism

Substances

  • Lipocalins
  • PPAR gamma
  • Intramolecular Oxidoreductases
  • prostaglandin R2 D-isomerase