Molecular Background of Leak K+ Currents: Two-Pore Domain Potassium Channels

被引:667
作者
Enyedi, Peter [1 ]
Czirjak, Gabor [1 ]
机构
[1] Semmelweis Univ, Dept Physiol, H-1444 Budapest, Hungary
关键词
POLYUNSATURATED FATTY-ACIDS; RAT CAROTID-BODY; CEREBELLAR GRANULE NEURONS; 2 PORE DOMAINS; SMOOTH-MUSCLE-CELLS; THALAMOCORTICAL RELAY NEURONS; ADRENAL GLOMERULOSA CELLS; ROOT GANGLION NEURONS; PROTEIN-KINASE-C; ALTERNATIVE TRANSLATION INITIATION;
D O I
10.1152/physrev.00029.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Enyedi P, Czirjak G. Molecular Background of Leak K+ Currents: Two-Pore Domain Potassium Channels. Physiol Rev 90: 559-605, 2010; doi:10.1152/physrev.00029.2009.-Two-pore domain K+ (K-2P) channels give rise to leak (also called background) K+ currents. The well-known role of background K+ currents is to stabilize the negative resting membrane potential and counterbalance depolarization. However, it has become apparent in the past decade (during the detailed examination of the cloned and corresponding native K-2P channel types) that this primary hyperpolarizing action is not performed passively. The K-2P channels are regulated by a wide variety of voltage-independent factors. Basic physicochemical parameters (e. g., pH, temperature, membrane stretch) and also several intracellular signaling pathways substantially and specifically modulate the different members of the six K-2P channel subfamilies (TWIK, TREK, TASK, TALK, THIK, and TRESK). The deep implication in diverse physiological processes, the circumscribed expression pattern of the different channels, and the interesting pharmacological profile brought the K-2P channel family into the spotlight. In this review, we focus on the physiological roles of K-2P channels in the most extensively investigated cell types, with special emphasis on the molecular mechanisms of channel regulation.
引用
收藏
页码:559 / 605
页数:47
相关论文
共 357 条
[111]   Altered acetylcholine, bradykinin and cutaneous pressure-induced vasodilation in mice lacking the TREK1 potassium channel: the endothelial link [J].
Garry, Ambroise ;
Fromy, Berengere ;
Blondeau, Nicolas ;
Henrion, Daniel ;
Brau, Frederic ;
Gounon, Pierre ;
Guy, Nicolas ;
Heurteaux, Catherine ;
Lazdunski, Michel ;
Saumet, Jean Louis .
EMBO REPORTS, 2007, 8 (04) :354-359
[112]   p11, an annexin II subunit, an auxiliary protein associated with the background K+ channel, TASK-1 [J].
Girard, C ;
Tinel, N ;
Terrenoire, C ;
Romey, G ;
Lazdunski, M ;
Borsotto, M .
EMBO JOURNAL, 2002, 21 (17) :4439-4448
[113]   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
[114]   Potential, impedance, and rectification in membranes [J].
Goldman, DE .
JOURNAL OF GENERAL PHYSIOLOGY, 1943, 27 (01) :37-60
[115]   Sequence and function of the two P domain potassium channels: Implications of an emerging superfamily [J].
Goldstein, SAN ;
Wang, KW ;
Ilan, N ;
Pausch, MH .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (01) :13-20
[116]   International Union of Pharmacology. LV. Nomenclature and molecular relationships of two-P potassium channels [J].
Goldstein, SAN ;
Bayliss, DA ;
Kim, D ;
Lesage, F ;
Plant, LD ;
Rajan, S .
PHARMACOLOGICAL REVIEWS, 2005, 57 (04) :527-540
[117]   ORK1, a potassium-selective leak channel with two pore domains cloned from Drosophila melanogaster by expression in Saccharomyces cerevisiae [J].
Goldstein, SAN ;
Price, LA ;
Rosenthal, DN ;
Pausch, MH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) :13256-13261
[118]   Investigation of the role of TASK-2 channels in rat pulmonary arteries;: pharmacological and functional studies following RNA interference procedures [J].
Gönczi, M ;
Szentandrássy, N ;
Johnson, IT ;
Heagerty, AM ;
Weston, AH .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 147 (05) :496-505
[119]   Deletion of TASK1 and TASK3 channels disrupts intrinsic excitability but does not abolish glucose or pH responses of orexin/hypocretin neurons [J].
Gonzalez, J. A. ;
Jensen, Lise T. ;
Doyle, Susan E. ;
Miranda-Anaya, Manuel ;
Menaker, Michael ;
Fugger, Lars ;
Bayliss, Douglas A. ;
Burdakov, Denis .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2009, 30 (01) :57-64
[120]   Expression of a two-pore domain K+ channel (TASK-1) in developing avian and mouse ventricular conduction systems [J].
Graham, V ;
Zhang, HT ;
Willis, S ;
Creazzo, TL .
DEVELOPMENTAL DYNAMICS, 2006, 235 (01) :143-151