Deleterious impact of Pseudomonas aeruginosa on cystic fibrosis transmembrane conductance regulator function and rescue in airway epithelial cells
- PMID: 25792634
- DOI: 10.1183/09031936.00076214
Deleterious impact of Pseudomonas aeruginosa on cystic fibrosis transmembrane conductance regulator function and rescue in airway epithelial cells
Abstract
The epithelial response to bacterial airway infection, a common feature of lung diseases such as chronic obstructive pulmonary disease and cystic fibrosis, has been extensively studied. However, its impact on cystic fibrosis transmembrane conductance regulator (CFTR) channel function is not clearly defined. Our aims were, therefore, to evaluate the effect of Pseudomonas aeruginosa on CFTR function and expression in non-cystic fibrosis airway epithelial cells, and to investigate its impact on ΔF508-CFTR rescue by the VRT-325 corrector in cystic fibrosis cells. CFTR expression/maturation was evaluated by immunoblotting and its function by short-circuit current measurements. A 24-h exposure to P. aeruginosa diffusible material (PsaDM) reduced CFTR currents as well as total and membrane protein expression of the wildtype (wt) CFTR protein in CFBE-wt cells. In CFBE-ΔF508 cells, PsaDM severely reduced CFTR maturation and current rescue induced by VRT-325. We also confirmed a deleterious impact of PsaDM on wt-CFTR currents in non-cystic fibrosis primary airway cells as well as on the rescue of ΔF508-CFTR function induced by VRT-325 in primary cystic fibrosis cells. These findings show that CFTR function could be impaired in non-cystic fibrosis patients infected by P. aeruginosa. Our data also suggest that CFTR corrector efficiency may be affected by infectious components, which should be taken into account in screening assays of correctors.
Copyright ©ERS 2015.
Similar articles
-
Quorum Sensing Down-Regulation Counteracts the Negative Impact of Pseudomonas aeruginosa on CFTR Channel Expression, Function and Rescue in Human Airway Epithelial Cells.Front Cell Infect Microbiol. 2017 Nov 10;7:470. doi: 10.3389/fcimb.2017.00470. eCollection 2017. Front Cell Infect Microbiol. 2017. PMID: 29177135 Free PMC article.
-
Improvement of defective cystic fibrosis airway epithelial wound repair after CFTR rescue.Eur Respir J. 2012 Dec;40(6):1390-400. doi: 10.1183/09031936.00221711. Epub 2012 Apr 10. Eur Respir J. 2012. PMID: 22496330
-
The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability.Am J Physiol Lung Cell Mol Physiol. 2008 Jul;295(1):L25-37. doi: 10.1152/ajplung.00391.2007. Epub 2008 Mar 21. Am J Physiol Lung Cell Mol Physiol. 2008. PMID: 18359885 Free PMC article.
-
Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.Proc Natl Acad Sci U S A. 2000 Aug 1;97(16):8822-8. doi: 10.1073/pnas.97.16.8822. Proc Natl Acad Sci U S A. 2000. PMID: 10922041 Free PMC article. Review.
-
The role of the CFTR in susceptibility to Pseudomonas aeruginosa infections in cystic fibrosis.Trends Microbiol. 2000 Nov;8(11):514-20. doi: 10.1016/s0966-842x(00)01872-2. Trends Microbiol. 2000. PMID: 11121762 Review.
Cited by
-
The era of CFTR modulators: improvements made and remaining challenges.Breathe (Sheff). 2020 Jun;16(2):200016. doi: 10.1183/20734735.0016-2020. Breathe (Sheff). 2020. PMID: 33304402 Free PMC article.
-
Pseudomonas aeruginosa LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator-IL-6-antimicrobial-repair pathway.Thorax. 2018 Jan;73(1):49-61. doi: 10.1136/thoraxjnl-2017-210298. Epub 2017 Aug 8. Thorax. 2018. PMID: 28790180 Free PMC article.
-
Cystic fibrosis transmembrane conductance regulator in COPD: a role in respiratory epithelium and beyond.Eur Respir J. 2023 Apr 1;61(4):2201307. doi: 10.1183/13993003.01307-2022. Print 2023 Apr. Eur Respir J. 2023. PMID: 37003609 Free PMC article. Review.
-
Lumacaftor and Matrine: Possible Therapeutic Combination to Counteract the Inflammatory Process in Cystic Fibrosis.Biomolecules. 2021 Mar 13;11(3):422. doi: 10.3390/biom11030422. Biomolecules. 2021. PMID: 33805605 Free PMC article.
-
Modulation of Ion Transport to Restore Airway Hydration in Cystic Fibrosis.Genes (Basel). 2021 Mar 22;12(3):453. doi: 10.3390/genes12030453. Genes (Basel). 2021. PMID: 33810137 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical