| Literature DB >> 31116581 |
Nadzeya Marozkina1, Jürgen Bosch1, Calvin Cotton1, Laura Smith1, James Seckler1, Khalequz Zaman1, Shagufta Rehman2, Ammasi Periasamy2, Herbert Gaston3, Ghaith Altawallbeh1, Michael Davis4, David R Jones5, Robert Schilz6, Scott H Randell7, Benjamin Gaston1,8.
Abstract
The mechanisms by which transepithelial pressure changes observed during exercise and airway clearance can benefit lung health are challenging to study. Here, we have studied 117 mature, fully ciliated airway epithelial cell filters grown at air-liquid interface grown from 10 cystic fibrosis (CF) and 19 control subjects. These were exposed to cyclic increases in apical air pressure of 15 cmH2O for varying times. We measured the effect on proteins relevant to lung health, with a focus on the CF transmembrane regulator (CFTR). Immunoflourescence and immunoblot data were concordant in demonstrating that air pressure increased F508Del CFTR expression and maturation. This effect was in part dependent on the presence of cilia, on Ca2+ influx, and on formation of nitrogen oxides. These data provide a mechanosensory mechanism by which changes in luminal air pressure, like those observed during exercise and airway clearance, can affect epithelial protein expression and benefit patients with diseases of the airways.Entities:
Keywords: -nitrosocysteine; airway cilia; airway clearance; airway pressure; cystic fibrosis
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Year: 2019 PMID: 31116581 PMCID: PMC6734384 DOI: 10.1152/ajplung.00020.2019
Source DB: PubMed Journal: Am J Physiol Lung Cell Mol Physiol ISSN: 1040-0605 Impact factor: 5.464