Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells
- 1 January 1995
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Cell Physiology
- Vol. 268 (1) , C243-C251
- https://doi.org/10.1152/ajpcell.1995.268.1.c243
Abstract
When nonepithelial cell types expressing the delta F508-cystic fibrosis transmembrane conductance regulator (CFTR) mutation are grown at reduced temperatures, the mutant protein can be properly processed. The effect of low temperatures on Cl- channel activity in airway epithelial cells that endogenously express the delta F508-CFTR mutation has not been investigated. Therefore, we examined the effect of incubation temperature on both CFTR and outwardly rectifying Cl- channel (ORCC) activity in normal, in cystic fibrosis (CF)-affected, and in wild-type CFTR-complemented CF airway epithelia with use of a combination of inside-out and whole cell patch-clamp recording, 36Cl- efflux assays, and immunocytochemistry. We report that incubation of CF-affected airway epithelial cells at 25-27 degrees C is associated with the appearance of a protein kinase A-stimulated CFTR-like Cl- conductance. In addition to the appearance of CFTR Cl- channel activity, there is, however, a decrease in the number of active ORCC when cells are grown at 25-27 degrees C, suggesting that the decrease in incubation temperature may be associated with multiple alterations in ion channel expression and/or regulation in airway epithelial cells.Keywords
This publication has 8 references indexed in Scilit:
- The cystic fibrosis mutation (ΔF508) does not influence the chloride channel activity of CFTRNature Genetics, 1993
- GTP-binding proteins inhibit cAMP activation of chloride channels in cystic fibrosis airway epithelial cells.Proceedings of the National Academy of Sciences, 1992
- Differential Localization of the Cystic Fibrosis Transmembrane Conductance Regulator in Normal and Cystic Fibrosis Airway EpitheliumAmerican Journal of Respiratory Cell and Molecular Biology, 1992
- Cystic fibrosis transmembrane conductance regulator: A chloride channel with novel regulationNeuron, 1992
- CFTR protein expression in primary and cultured epithelia.Proceedings of the National Academy of Sciences, 1992
- A Cystic Fibrosis Bronchial Epithelial Cell Line: Immortalization by Adeno-12-SV40 InfectionAmerican Journal of Respiratory Cell and Molecular Biology, 1991
- Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epitheliumNature, 1988
- Phosphorylation fails to activate chloride channels from cystic fibrosis airway cellsNature, 1987