Heitzmann, D. and Grahammer, F. and von Hahn, T. and Schmitt-Graff, A. and Romeo, E. and Nitschke, R. and Gerlach, U. and Lang, H. J. and Verrey, F. and Barhanin, J. and Warth, Richard (2004) Heteromeric KCNE2/KCNQ1 potassium channels in the luminal membrane of gastric parietal cells. JOURNAL OF PHYSIOLOGY-LONDON, 561 (2). pp. 547-557. ISSN 0022-3751, 1469-7793
Full text not available from this repository. (Request a copy)Abstract
Recently, we and others have shown that luminal K+ recycling via KCNQ1 K+ channels is required for gastric H+ secretion. Inhibition of KCNQ1 by the chromanol 293B strongly diminished H+ secretion. The present study aims at clarifying KCNQ1 subunit composition, subcellular localization, regulation and pharmacology in parietal cells. Using in situ hybridization and immunofluorescence techniques, we identified KCNE2 as the beta subunit of KCNQ1 in the luminal membrane compartment of parietal cells. Expressed in COS cells, hKCNE2/hKCNQ1 channels were activated by acidic PH, PIP2, cAMP and purinergic receptor stimulation. Qualitatively similar results were obtained in mouse parietal cells. Confocal microscopy revealed stimulation-induced translocation of H+,K+-ATPase from tubulovesicles towards the luminal pole of parietal cells, whereas distribution of KCNQ1 K+ channels did not change to the same extent. In COS cells the 293B-related substance IKs124 blocked hKCNE2/hKCNQ1 with an IC50 of 8 nM. Inhibition of hKCNE1- and hKCNE3-containing channels was weaker with IC50 values of 370 and 440 nM, respectively. In conclusion, KCNQ1 coassembles with KCNE2 to form acid-activated luminal K+ channels of parietal cells. KCNQ1/KCNE2 is activated during acid secretion via several pathways but probably not by targeting of the channel to the membrane. IKs124 could serve as a leading compound in the development of subunit-specific KCNE2/KCNQ1 blockers to treat peptic ulcers.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | ACID-SECRETION; K+ CHANNELS; CARDIAC-ARRHYTHMIAS; APICAL MEMBRANE; CL CONDUCTANCES; KNOCKOUT MOUSE; OXYNTIC CELLS; KCNQ1; GENE; K(V)LQT1; |
| Subjects: | 500 Science > 570 Life sciences |
| Divisions: | Biology, Preclinical Medicine > Institut für Physiologie > Prof. Dr. Richard Warth |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 21 Jun 2021 10:23 |
| Last Modified: | 21 Jun 2021 10:23 |
| URI: | https://pred.uni-regensburg.de/id/eprint/36913 |
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