Asthmatic bronchial epithelium is more susceptible to oxidant-induced apoptosis

Am J Respir Cell Mol Biol. 2002 Aug;27(2):179-85. doi: 10.1165/ajrcmb.27.2.4699.


Abnormal apoptotic mechanisms are associated with disease pathogenesis. Because the asthmatic bronchial epithelium is characteristically damaged with loss of columnar epithelial cells, we postulated that this is due to unscheduled apoptosis. Using an antibody directed toward the caspase cleavage product of poly(ADP-ribose) polymerase, immunohistochemistry applied to endobronchial biopsies showed higher levels of staining in the bronchial epithelium of subjects with asthma as compared with normal control subjects (% epithelial staining [median (range) = 10.5 (1.4-24.5) versus 0.4 (0.0-9.7)]; P < 0.001). Because we were unable to determine whether this difference was due to ongoing inflammation in vivo, cultures of normal and asthmatic bronchial epithelial cells were used to study apoptosis in vitro. In complete growth medium, these cells showed no difference in their rate of proliferation or viability. However, cells from subjects with asthma were more susceptible to the apoptotic effects of H2O2 than cells from normal control subjects (% apoptotic cells = 32.2 [8.8-54.9] versus 14.3 [6.4-24.7]; P < 0.05), even though both were similarly affected by treatment with actinomycin D. These data indicate that the susceptibility of asthmatic bronchial epithelium to oxidants is greater than normal. This susceptibility may contribute to the rising trends in asthma associated with air pollution and diets low in antioxidants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Apoptosis*
  • Asthma / physiopathology*
  • Biopsy
  • Bronchi / pathology
  • Bronchi / physiopathology*
  • Cell Biology
  • Cells, Cultured
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Female
  • Flow Cytometry
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Male
  • Middle Aged
  • Oxidants / pharmacology*
  • Poly(ADP-ribose) Polymerases / metabolism
  • Respiratory Mucosa / metabolism
  • Respiratory Mucosa / pathology
  • Respiratory Mucosa / physiopathology*
  • Tumor Necrosis Factor-alpha / pharmacology


  • Oxidants
  • Tumor Necrosis Factor-alpha
  • Hydrogen Peroxide
  • Poly(ADP-ribose) Polymerases