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March 7, 2001FEBS Letters153 citations

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

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NDNiels DecherMMMarcel MaierWDWerner Dittrich

Structured PICO

P
Population
Xenopus oocytes expressing TASK-4 and human tissue transcripts
I
Intervention
Application of channel blockers (barium, quinine, bupivacaine, lidocaine, tetraethylammonium, 4-aminopyridine, Cs+) and changes in extracellular pH
O
Outcome
K(+) currents and pH sensitivitysurrogate

Identifies and characterizes TASK-4 as a novel alkaline pH-sensitive two-pore domain potassium channel expressed in multiple human tissues including the heart.

Abstract

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 by 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.

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Cite This Study

Decher et al. (2001) studied this question.

synapsesocial.com/papers/69ff969eb124fe58198584c8https://doi.org/10.1016/s0014-5793(01)02222-0
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