Increased activation of fibrocytes in patients with chronic obstructive asthma through an epidermal growth factor receptor-dependent pathway

J Allergy Clin Immunol. 2012 May;129(5):1367-76. doi: 10.1016/j.jaci.2012.01.038. Epub 2012 Feb 9.

Abstract

Background: Fibrocytes are circulating progenitor cells that are increased in asthmatic patients with chronic obstructive asthma (COA) and rapid decrease in lung function. Fibrocytes from patients with COA have a greater capacity for proliferation and differentiation.

Objective: We investigated whether epidermal growth factor receptor (EGFR) activation mediated the proliferation of fibrocytes in patients with COA and whether oxidative stress was involved in this activation.

Methods: Circulating fibrocytes from nonadherent non-T-cell mononuclear cell fractions from healthy subjects, asthmatic patients with normal pulmonary function, and patients with COA were determined by using flow cytometric coexpression of collagen I, CD45, and CD34 or EGFR or a disintegrin and metalloprotease domain 17 and placed in culture.

Results: Expression of EGFR was increased in fibrocytes from patients with COA compared with that seen in patients with NPF. AG1478 and gefitinib, inhibitors of EGFR tyrosine kinase, reduced fibrocyte proliferation and myofibroblast transformation. Increased expression of EGFR and fibrocyte proliferation and transformation were induced by hydrogen peroxide, and these effects were inhibited by N-acetylcysteine.

Conclusions: Enhanced fibrocyte proliferation and transformation found in patients with COA might be mediated through an oxidant-sensitive EGFR-dependent pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / metabolism
  • ADAM17 Protein
  • Acetylcysteine / pharmacology
  • Adult
  • Antigens, CD34 / metabolism
  • Asthma / complications
  • Asthma / drug therapy
  • Asthma / metabolism*
  • Asthma / pathology
  • Blood Cells / drug effects
  • Blood Cells / metabolism*
  • Blood Cells / pathology
  • Cell Proliferation / drug effects
  • Cell Transformation, Neoplastic / drug effects
  • Cells, Cultured
  • Collagen Type I / metabolism
  • ErbB Receptors / metabolism*
  • Female
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology
  • Follow-Up Studies
  • Gefitinib
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Leukocyte Common Antigens / metabolism
  • Male
  • Middle Aged
  • Oxidative Stress
  • Pulmonary Disease, Chronic Obstructive / complications
  • Pulmonary Disease, Chronic Obstructive / drug therapy
  • Pulmonary Disease, Chronic Obstructive / metabolism*
  • Pulmonary Disease, Chronic Obstructive / pathology
  • Quinazolines / pharmacology
  • Quinazolines / therapeutic use
  • Respiratory Function Tests
  • Signal Transduction
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Stem Cells / pathology
  • Tyrphostins / pharmacology

Substances

  • Antigens, CD34
  • Collagen Type I
  • Quinazolines
  • Tyrphostins
  • RTKI cpd
  • Hydrogen Peroxide
  • EGFR protein, human
  • ErbB Receptors
  • Leukocyte Common Antigens
  • ADAM Proteins
  • ADAM17 Protein
  • Gefitinib
  • Acetylcysteine