Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel

被引:83
作者
Meadows, HJ [1 ]
Randall, AD [1 ]
机构
[1] SmithKline Beecham Pharmaceut, Neurosci Res, Harlow CM19 5AW, Essex, England
关键词
potassium channel; human; membrane potential;
D O I
10.1016/S0028-3908(00)00189-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Human TASK-3 (hTASK-3) is a recently identified member of the two-pore domain potassium channel (2PDKC) family which in man is predominantly expressed in the cerebellum. Previous preliminary examination of this channel indicates that when expressed in Xenopus oocytes, it produces a K+ selective background conductance and consequent shift in resting membrane potential, thus mimicking other 2PDKC. Here we describe some additional functional and pharmacological aspects of hTASK-3-mediated conductances expressed in both Xenopus oocytes and HEK293 cells. hTASK-3 expression produces steady-state currents that approximate Goldman-Hodgkin-Katz behaviour with respect to membrane potential. Despite this, voltage steps from -80 mV to potentials >similar to -20 mV induce currents that exhibit a clear time-dependent increase in current amplitude. Kinetically, this increase in current was well fit by a single exponential, the time constant of which was similar to 10 ms and appeared independent of test potential, between -20 and +80 mV. In HEK293 cells hTASK-3 currents were inhibited by extracellular acidosis with a mid-point for inhibition of pH 6.4. Furthermore, the activity of TASK-3 was potentiated by the volatile anaesthetic halothane but inhibited by the local anaesthetic bupivacaine. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:551 / 559
页数:9
相关论文
共 31 条
[21]   DETERMINATION OF THE SUBUNIT STOICHIOMETRY OF A VOLTAGE-ACTIVATED POTASSIUM CHANNEL [J].
MACKINNON, R .
NATURE, 1991, 350 (6315) :232-235
[22]   Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel [J].
Meadows, HJ ;
Benham, CD ;
Cairns, W ;
Gloger, I ;
Jennings, C ;
Medhurst, AD ;
Murdock, P ;
Chapman, CG .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2000, 439 (06) :714-722
[23]  
PATE, J BIOL CHEM, V275, P28722
[24]   Inhalational anesthetics activate two-pore-domain background K+ channels [J].
Patel, AJ ;
Honoré, E ;
Lesage, F ;
Fink, M ;
Romey, G ;
Lazdunski, M .
NATURE NEUROSCIENCE, 1999, 2 (05) :422-426
[25]   Identification and cloning of TWIK-originated similarity sequence (TOSS):: a novel human 2-pore K+ channel principal subunit [J].
Pountney, DJ ;
Gulkarov, I ;
Vega-Saenz de Miera, E ;
Holmes, D ;
Saganich, M ;
Rudy, B ;
Artman, M ;
Coetzee, WA .
FEBS LETTERS, 1999, 450 (03) :191-196
[26]   TASK-3, a novel tandem pore domain acid-sensitive K+ channel -: An extracellular histidine as pH sensor [J].
Rajan, S ;
Wischmeyer, E ;
Liu, GX ;
Müller, RP ;
Daut, J ;
Karschin, A ;
Derst, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (22) :16650-16657
[27]   Cloning and expression of a novel pH-sensitive two pore domain K+ channel from human kidney [J].
Reyes, R ;
Duprat, F ;
Lesage, F ;
Fink, M ;
Salinas, M ;
Farman, N ;
Lazdunski, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (47) :30863-30869
[28]   Cloning of a new mouse two-P domain channel subunit and a human homologue with a unique pore structure [J].
Salinas, M ;
Reyes, R ;
Lesage, F ;
Fosset, M ;
Heurteaux, C ;
Romey, G ;
Lazdunski, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :11751-11760
[29]  
Siesjo BK, 1996, ADV NEUROL, V71, P209
[30]   The TASK-1 two-pore domain K+ channel is a molecular substrate for neuronal effects of inhalation anesthetics [J].
Sirois, JE ;
Lei, QB ;
Talley, EM ;
Lynch, C ;
Bayliss, DA .
JOURNAL OF NEUROSCIENCE, 2000, 20 (17) :6347-6354