Increased extracellular vesicles mediate inflammatory signalling in cystic fibrosis. Issue 6 (7th April 2020)

• Record Type: Journal Article
• Authors: Useckaite, Zivile; Ward, Mark P; Trappe, Anne; Reilly, Rebecca; Lennon, Jenny; Davage, Holly; Matallanas, David; Cassidy, Hilary; Dillon, Eugene T; Brennan, Kiva; Doyle, Sarah L; Carter, Suzanne; Donnelly, Seamas; Linnane, Barry; McKone, Edward F; McNally, Paul; Coppinger, Judith A
• Is Part Of: Thorax. Volume 75:Issue 6(2020)
• Page Start: 449
• Page End: 458
• Publication Date: 2020-04-07
• Subjects: cystic fibrosis -- paediatric lung disaese -- neutrophil biology; Chest -- Diseases -- Periodicals; Thorax; Chest -- Diseases; Periodicals; Periodicals; 617.54
• DOI: 10.1136/thoraxjnl-2019-214027
• Languages: English
• ISSNs: 0040-6376

Abstract

Abstract : Rationale: Mutations in the cystic fibrosis transmembrane regulator ( CFTR ) gene form the basis of cystic fibrosis (CF). There remains an important knowledge gap in CF as to how diminished CFTR activity leads to the dominant inflammatory response within CF airways. Objectives: To investigate if extracellular vesicles (EVs) contribute to inflammatory signalling in CF. Methods: EVs released from CFBE41o-, CuFi-5, 16HBE14o- and NuLi-1 cells were characterised by nanoparticle tracking analysis (NTA). EVs isolated from bronchoalveolar lavage fluid (BALF) from 30 people with CF (PWCF) were analysed by NTA and mass spectrometry and compared with controls. Neutrophils were isolated from the blood of 8 PWCF to examine neutrophil migration in the presence of CFBE41o- EVs. Results: A significantly higher level of EVs were released from CFBE41o- (p<0.0001) and CuFi-5 (p=0.0209) relative to control cell lines. A significantly higher level of EVs were detected in BALF of PWCF, in three different age groups relative to controls (p=0.01, 0.001, 0.002). A significantly lower level of EVs were released from CFBE41o- (p<0.001) and CuFi-5 (p=0.0002) cell lines treated with CFTR modulators. Significant changes in the protein expression of 126 unique proteins was determined in EVs obtained from the BALF of PWCF of different age groups (p<0.001–0.05). A significant increase in chemotaxis of neutrophils derived from PWCF was observed in the presence of CFBE41o EVs (p=0.0024) compared with controls. Conclusion: This study demonstrates that EVs are produced in CF airway cells, have differential protein expression at different ages and drive neutrophil recruitment in CF.