Characterization of TASK-4, a novel member of the pH-sensitive, two-pore domain potassium channel family

被引:120
作者
Decher, N [1 ]
Maier, M [1 ]
Dittrich, W [1 ]
Gassenhuber, J [1 ]
Brüggemann, A [1 ]
Busch, AE [1 ]
Steinmeyer, K [1 ]
机构
[1] Aventis Pharma Deutschland GmbH, DG Cardiovasc Dis, D-65926 Frankfurt, Germany
关键词
cloning; TASK; two-pore domain K+ channel; anesthetic;
D O I
10.1016/S0014-5793(01)02222-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the primary sequence of TASK-4, a novel member of the acid-sensitive subfamily of tandem pore K+ channels. TASK-4 transcripts are widely expressed in humans, with highest levels in liver, lung, pancreas, placenta, aorta and heart. In Xenopus oocytes TASK-4 generated K+ currents displaying a marked outward rectification which was lost bg. elevation of extracellular K+. TASK-4 currents were efficiently blocked by barium (83% inhibition at 2 mM), only weakly inhibited by 1 mM concentrations of quinine, bupivacaine and lidocaine, but not blocked by tetraethylammonium, 4-aminopyridine and Cs+. TASK-4 was sensitive to extracellular pH, but in contrast to other TASK channels, pH sensitivity was shifted to more alkaline pH, Thus, TASK-4 in concert with other TASK channels might regulate cellular membrane potential over a wide range of extracellular pH, (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V, All rights reserved.
引用
收藏
页码:84 / +
页数:7
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