The family of K2P channels: salient structural and functional properties

被引:166
作者
Feliciangeli, Sylvain
Chatelain, Frank C.
Bichet, Delphine
Lesage, Florian
机构
[1] CNRS, Inst Pharmacol Mol & Cellulaire, LabEx ICST, F-06560 Valbonne, France
[2] Univ Nice Sophia Antipolis, F-06560 Valbonne, France
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2015年 / 593卷 / 12期
关键词
DOMAIN K+ CHANNELS; UNION-OF-PHARMACOLOGY; BACKGROUND POTASSIUM CHANNEL; POLYUNSATURATED FATTY-ACIDS; CHANGE ION SELECTIVITY; 2-PORE DOMAIN; MOLECULAR RELATIONSHIPS; ARACHIDONIC-ACID; TASK CHANNELS; EXTRACELLULAR HISTIDINE;
D O I
10.1113/jphysiol.2014.287268
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Potassium channels participate in many biological functions, from ion homeostasis to generation and modulation of the electrical membrane potential. They are involved in a large variety of diseases. In the human genome, 15 genes code for K+ channels with two pore domains (K-2P). These channels form dimers of pore-forming subunits that produce background conductances finely regulated by a range of natural and chemical effectors, including signalling lipids, temperature, pressure, pH, antidepressants and volatile anaesthetics. Since the cloning of TWIK1, the prototypical member of this family, a lot of work has been carried out on their structure and biology. These studies are still in progress, but data gathered so far show that K-2P channels are central players in many processes, including ion homeostasis, hormone secretion, cell development and excitability. A growing number of studies underline their implication in physiopathological mechanisms, such as vascular and pulmonary hypertension, cardiac arrhythmias, nociception, neuroprotection and depression. This review gives a synthetic view of the most noticeable features of these channels.
引用
收藏
页码:2587 / 2603
页数:17
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