Loss of ciliated cells and altered airway epithelial integrity in cystic fibrosis

J Cyst Fibros. 2021 Nov;20(6):e129-e139. doi: 10.1016/j.jcf.2021.09.019. Epub 2021 Oct 15.

Abstract

Background: In cystic fibrosis, the respiratory epithelium is the target tissue of both the genetic abnormality of the disease and of external aggressions, notably by pathogens (Pseudomonas aeruginosa). A detailed characterisation of the cystic fibrosis bronchial epithelium is however lacking, as most previous studies focused on the nasal epithelium or on cell lines. This study aimed to characterise the abnormal phenotype and epithelial-to-mesenchymal transition in cystic fibrosis bronchial epithelium and to evaluate in cell cultures whether abnormalities persist ex vivo.

Methods: Explant lung tissues (n = 44) were assessed for bronchial epithelial cell phenotyping by immunostaining. Human bronchial epithelial cells were derived from basal cells isolated from cystic fibrosis patients or control donors and cultured in air-liquid interface for 2, 4 or 6 weeks.

Results: Enhanced mucin 5AC and decreased β-tubulin expression were observed in cystic fibrosis airways reflecting a decreased ciliated/goblet cell ratio, associated with increased number of vimentin-positive cells, indicating epithelial-to-mesenchymal transition process. These features were recapitulated in vitro, in cystic fibrosis-derived reconstituted epithelium. However, they were not induced by CFTR inhibition or Pseudomonas infection, and most abnormalities tended to disappear in long-term culture (6 weeks) except for increased fibronectin release, an epithelial-to-mesenchymal transition marker.

Conclusions: This study provides new insights into airway epithelial changes in cystic fibrosis, which are imprinted through an acquired mechanism that we could not relate to CFTR function.

Keywords: Epithelial differentiation; Epithelial-to-mesenchymal transition; Respiratory epithelium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Bronchi / cytology*
  • Cell Differentiation
  • Cystic Fibrosis / metabolism*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mucin 5AC / metabolism
  • Respiratory Mucosa / cytology*
  • Tubulin / metabolism

Substances

  • Biomarkers
  • MUC5AC protein, human
  • Mucin 5AC
  • Tubulin