Surface Hydration Protects Cystic Fibrosis Airways from Infection by Restoring Junctional Networks

Cells. 2022 May 9;11(9):1587. doi: 10.3390/cells11091587.

Abstract

Defective hydration of airway surface mucosa is associated with recurrent lung infection in cystic fibrosis (CF), a disease caused by CF transmembrane conductance regulator (CFTR) gene mutations. Whether the composition and/or presence of an airway surface liquid (ASL) is sufficient to prevent infection remains unclear. The susceptibility to infection of polarized wild type and CFTR knockdown (CFTR-KD) airway epithelial cells was determined in the presence or absence of a healthy ASL or physiological saline. CFTR-KD epithelia exhibited strong ASL volume reduction, enhanced susceptibility to infection, and reduced junctional integrity. Interestingly, the presence of an apical physiological saline alleviated disruption of the airway epithelial barrier by stimulating essential junctional protein expression. Thus, rehydrated CFTR-KD cells were protected from infection despite normally intense bacterial growth. This study indicates that an epithelial integrity gatekeeper is modulated by the presence of an apical liquid volume, irrespective of the liquid's composition and of expression of a functional CFTR.

Keywords: P. aeruginosa; airway surface liquid; cystic fibrosis; epithelium integrity; mucosal immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cystic Fibrosis Transmembrane Conductance Regulator* / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator* / metabolism
  • Cystic Fibrosis* / metabolism
  • Epithelial Cells / metabolism
  • Humans
  • Ion Transport
  • Respiratory Mucosa / metabolism

Substances

  • Cystic Fibrosis Transmembrane Conductance Regulator

Grants and funding

This research was funded by the Swiss National Science Foundation, grant number 310030_204167/1.