[Cell apoptosis and the associated signal expression in epithelial cells from patients with idiopathic pulmonary fibrosis]

Zhonghua Jie He He Hu Xi Za Zhi. 2007 Oct;30(10):767-70.
[Article in Chinese]

Abstract

Objective: To investigate the changes and significance of cell apoptosis, Fas/FasL and P53 protein in epithelial cells from patients with idiopathic pulmonary fibrosis (IPF).

Methods: Cell apoptosis and the expressions of Fas/FasL and P53 protein in lung tissues from 12 patients with IPF (IPF group) and 10 normal controls (control group) were detected by terminal deoxynucleotide transferase-mediated deoxyuridine triphosphate-biotin nick end-labeling (TUNEL) and immunohistochemistry.

Results: Compared with the control group (0/10), the percentage of apoptosis in alveolar epithelial cells and bronchial cells of the IPF group (12/12) was higher. The percentage of Fas, FasL and P53 protein expressions (12/12, 12/12, 11/12) in alveolar epithelial cells of the IPF group were higher than those of the control group (5/10, 2/10, 0/10); and the percentage of Fas, FasL and P53 protein expressions (12/12, 12/12, 11/12) in bronchial cells of the IPF group were also higher than those of the control group (6/10, 3/10, 0/10). There was a significant correlation between the percentage of apoptosis and Fas/FasL and P53 protein expression (r=0.625-0.839, all P<0.01). The correlation of the Fas/FasL and P53 protein expression was also significant (r=0.571-0.760, all P<0.01).

Conclusion: The apoptosis percentage of epithelial cells and the expression of Fas/FasL and P53 protein are up-regulated in lung tissues of IPF, which may play an important role in the development of the disease.

MeSH terms

  • Adult
  • Aged
  • Apoptosis*
  • Bronchi / metabolism
  • Bronchi / pathology
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Fas Ligand Protein / biosynthesis
  • Female
  • Humans
  • Idiopathic Pulmonary Fibrosis / metabolism*
  • Idiopathic Pulmonary Fibrosis / pathology
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Lung / metabolism*
  • Lung / pathology
  • Male
  • Middle Aged
  • Pulmonary Alveoli / metabolism
  • Pulmonary Alveoli / pathology
  • Signal Transduction
  • Tumor Suppressor Protein p53 / metabolism
  • Up-Regulation
  • fas Receptor / biosynthesis

Substances

  • Fas Ligand Protein
  • Tumor Suppressor Protein p53
  • fas Receptor