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Updated: Oct 2, 2026

Real-Time, Semi-Automated Fluorescent Measurement of the Airway Surface Liquid pH of Primary Human Airway Epithelial Cells
Published on: June 13, 2019
Altered NaCl concentration of airway surface liquid in cystic fibrosis
1Department of Human Physiology, University of California - Davis, Davis, CA 95616-8664, USA. jhwiddicombe@ucdavis.edu
Abstract:
A novel isotopic technique suggests that the [Na] and [Cl] of airway surface liquid are both normally approximately 50 mM. In cystic fibrosis, lack of the functional cystic fibrosis transmembrane conductance regulator (CFTR) causes failure of transcellular Cl absorption, resulting in an elevation of [Na] and [Cl] of airway surface liquid to approximately 100 mM.
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