Characterization of four types of background potassium channels in rat cerebellar granule neurons

被引:103
作者
Han, J
Truell, J
Gnatenco, C
Kim, D
机构
[1] Finch Univ Hlth Sci Chicago Med Sch, Dept Physiol & Biophys, N Chicago, IL 60064 USA
[2] Gyeongsang Natl Univ, Sch Med, Dept Physiol, Chinju, South Korea
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2002年 / 542卷 / 02期
关键词
D O I
10.1113/jphysiol.2002.017590
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cerebellar granule neurons express a standing outward (background) K+ current (I-K,I-SO) that regulates the resting membrane potential and cell excitability. As several tandem-pore (2P) K+ channel mRNAs are highly expressed in cerebellar granule cells, we studied whether, and which, 2P K+ channels contribute to I-K,I-SO. I-K,I-SO was highly sensitive to changes in extracellular pH and was partially inhibited by acetylcholine, as reported previously. In cell-attached patches from cultured cerebellar granule neurons, four types of K+ channels were found to be active when membrane potential was held at -50 mV or +50 mV in symmetrical 140 mm KCl. Based on single-channel conductances, gating kinetics and modulation by pharmacological agents and pH, three K+ channels could be considered as functional correlates of TASK-1, TASK-3 and TREK-2, which are members of the 2P K+ channel family. The fourth K+ channel (Type 4) has not been described previously and its molecular correlate is not yet known. Based on the measurement of channel current densities, the Type 2 (TASK-3) and the Type 4 K+ channels were determined to be the major sources of I-K,I-SO in cultured cerebellar granule neurons. The Type 1 (TASK-1) and Type 3 (TREK-2) activities were relatively low throughout cell growth in culture (1 - 10 days). Similar to TASK-I and TASK-3, the Type 4 K+ channel was highly sensitive to changes in extracellular pH, showing a 78% inhibition by changing the extracellular pH from 7.3 to 6.3. The results of this study show that three 2P K+ channels and an additional pH-sensing K+ channel (Type 4) comprise the I-K,I-SO in cultured cerebellar granule neurons. Our results also show that the high sensitivity of I-K,I-SO to extracellular pH comes from the high sensitivity of Type 2 (TASK-3) and Type 4 K+ channels.
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收藏
页码:431 / 444
页数:14
相关论文
共 43 条
[11]   A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids [J].
Fink, M ;
Lesage, F ;
Duprat, F ;
Heurteaux, C ;
Reyes, R ;
Fosset, M ;
Lazdunski, M .
EMBO JOURNAL, 1998, 17 (12) :3297-3308
[12]   Cloning, functional expression and brain localization of a novel unconventional outward rectifier K+ channel [J].
Fink, M ;
Duprat, F ;
Lesage, F ;
Reyes, R ;
Romey, G ;
Heurteaux, C ;
Lazdunski, M .
EMBO JOURNAL, 1996, 15 (24) :6854-6862
[13]  
GALLO V, 1987, J NEUROSCI, V7, P2203
[14]   Genomic and functional characteristics of novel human pancreatic 2P domain K+ channels [J].
Girard, C ;
Duprat, F ;
Terrenoire, C ;
Tinel, N ;
Fosset, M ;
Romey, G ;
Lazdunski, M ;
Lesage, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 282 (01) :249-256
[15]   Potassium leak channels and the KCNK family of two-P-domain subunits [J].
Goldstein, SAN ;
Bockenhauer, D ;
O'Kelly, I ;
Zilberberg, N .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (03) :175-184
[16]   Expression pattern and functional characteristics of two novel splice variants of the two-pore-domain potassium channel TREK-2 [J].
Gu, WL ;
Schlichthörl, G ;
Hirsch, JR ;
Engels, H ;
Karschin, C ;
Karschin, A ;
Derst, C ;
Steinlein, OK ;
Daut, J .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 539 (03) :657-668
[17]   Inwardly rectifying potassium channels: Their molecular heterogeneity and function [J].
Isomoto, S ;
Kondo, C ;
Kurachi, Y .
JAPANESE JOURNAL OF PHYSIOLOGY, 1997, 47 (01) :11-39
[18]  
KARSCHIN C, 2002, NOL CELLULAR NEUROSC, V18, P632
[19]   TASK-5, a new member of the tandem-pore K+ channel family [J].
Kim, D ;
Gnatenco, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 284 (04) :923-930
[20]   ARACHIDONIC-ACID ACTIVATION OF A NEW FAMILY OF K+ CHANNELS IN CULTURED RAT NEURONAL CELLS [J].
KIM, DH ;
SLADEK, CD ;
AGUADOVELASCO, C ;
MATHIASEN, JR .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 484 (03) :643-660