Mechanism of sodium hyperabsorption in cultured cystic fibrosis nasal epithelium: a patch-clamp study
- 1 April 1994
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Cell Physiology
- Vol. 266 (4) , C1061-C1068
- https://doi.org/10.1152/ajpcell.1994.266.4.c1061
Abstract
Transepithelial Na+ absorption is increased two to three times in cystic fibrosis (CF) compared with normal (NL) airway epithelia. This increase has been associated with a higher Na+ permeability of the apical membrane of airway epithelial cells. Because Na+ absorption is electrogenic and abolished by amiloride, Na+ channels are thought to dominate the apical membrane Na+ permeability. Three Na+ channel-related mechanisms may explain the increase in apical Na+ permeability in CF cells: increased number of channels, increased single-channel conductance, and increased single-channel open probability. We compared the properties of Na(+)-permeable channels in the apical membrane of confluent preparations of human NL and CF nasal epithelial cells cultured on permeable supports. Na(+)-permeable channels were studied using the patch-clamp technique in the excised inside-out and cell-attached configurations. The same types of Na(+)-permeable channels were recorded in CF and NL cells. In excised patches, nonselective (Na+/K+) cation channels were recorded, and no differences between CF and NL were found in the properties, incidence, single-channel conductance, and single-channel open probability. In cell-attached patches, channels with a higher Na+ vs. K+ selectivity dominated. There was no difference between CF and NL cells in the incidence (18.8 vs. 21.4%, respectively) and conductance (17.2 +/- 2.8 vs. 21.4 +/- 1.5 pS, respectively) of Na(+)-permeable channels. However, the open probability was higher in CF cells compared with NL cells (30.0 +/- 3.4%, n = 6, vs. 15.0 +/- 3.9%, n = 13; P < 0.05). We conclude that, in CF nasal epithelial cells, the increase in Na+ permeability of the apical membrane results from an increase in the open probability of Na(+)-permeable channels in the apical membrane.Keywords
This publication has 14 references indexed in Scilit:
- Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.Journal of Clinical Investigation, 1991
- Non-selective cation and dysfunctional chloride cahnnels in the apical membrane of nasal epithelial cells cultured from cystic fibrosis patientsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1990
- Cystic fibrosis, pathophysiological and clinical aspectsEuropean Journal of Pediatrics, 1990
- A Pilot Study of Aerosolized Amiloride for the Treatment of Lung Disease in Cystic FibrosisNew England Journal of Medicine, 1990
- Chloride secretory response of cystic fibrosis human airway epithelia. Preservation of calcium but not protein kinase C- and A-dependent mechanisms.Journal of Clinical Investigation, 1989
- Cell Calcium Levels of Normal and Cystic Fibrosis Nasal EpitheliumPediatric Research, 1988
- Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.Journal of Clinical Investigation, 1987
- Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.Journal of Clinical Investigation, 1986
- Chloride uptake into cultured airway epithelial cells from cystic fibrosis patients and normal individuals.Proceedings of the National Academy of Sciences, 1985
- Increased Bioelectric Potential Difference across Respiratory Epithelia in Cystic FibrosisNew England Journal of Medicine, 1981