BACKGROUND: In CF patients, the defective ion transport causes a simultaneous reduction of fluid, Cl(-) and HCO3(-) secretion. We aimed to demonstrate that the resulting altered properties of mucus can be recovered using lumacaftor, a CFTR corrector. METHODS: The micro-rheology of non-CF and CF mucus was analysed using Multiple Particle Tracking. RESULTS: The diffusion coefficient of nano-beads imbedded in mucus from CF human bronchial epithelium was lower than in non-CF mucus, and the elastic and viscous moduli were higher. We found that 25% correction of F508del-CFTR mutation with lumacaftor was enough to improve significantly CF mucus properties. Surprisingly, also incubation with amiloride, a compound that reduces fluid absorption but might not change the secretion of HCO3(-) towards the airway surface fluid, improved CF mucus properties. CONCLUSION: CF mucus properties can be recovered by either improving the hydration of the airways or recovering Cl(-) and HCO3(-) secretion across the mutated protein treated with a corrector compound.

Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus / Gianotti, Ambra; Capurro, Valeria; Scudieri, Paolo; Galietta, Luis J. V.; Moran, Oscar; Zegarra-Moran, Olga. - In: JOURNAL OF CYSTIC FIBROSIS. - ISSN 1569-1993. - 15:3(2016), pp. 295-301. [10.1016/j.jcf.2015.11.003]

Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus

Galietta, Luis J. V.;
2016

Abstract

BACKGROUND: In CF patients, the defective ion transport causes a simultaneous reduction of fluid, Cl(-) and HCO3(-) secretion. We aimed to demonstrate that the resulting altered properties of mucus can be recovered using lumacaftor, a CFTR corrector. METHODS: The micro-rheology of non-CF and CF mucus was analysed using Multiple Particle Tracking. RESULTS: The diffusion coefficient of nano-beads imbedded in mucus from CF human bronchial epithelium was lower than in non-CF mucus, and the elastic and viscous moduli were higher. We found that 25% correction of F508del-CFTR mutation with lumacaftor was enough to improve significantly CF mucus properties. Surprisingly, also incubation with amiloride, a compound that reduces fluid absorption but might not change the secretion of HCO3(-) towards the airway surface fluid, improved CF mucus properties. CONCLUSION: CF mucus properties can be recovered by either improving the hydration of the airways or recovering Cl(-) and HCO3(-) secretion across the mutated protein treated with a corrector compound.
2016
Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus / Gianotti, Ambra; Capurro, Valeria; Scudieri, Paolo; Galietta, Luis J. V.; Moran, Oscar; Zegarra-Moran, Olga. - In: JOURNAL OF CYSTIC FIBROSIS. - ISSN 1569-1993. - 15:3(2016), pp. 295-301. [10.1016/j.jcf.2015.11.003]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/728873
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