Sodium channels as macromolecular complexes: Implications for inherited arrhythmia syndromes

被引:139
作者
Meadows, LS [1 ]
Isom, LL [1 ]
机构
[1] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
关键词
cardiac myocytes; channel physiology; sodium channel; auxilliary subunits; cell adhesion molecules;
D O I
10.1016/j.cardiores.2005.04.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mutations in cardiac ion channels and their auxiliary subunits can lead to life-threatening cardiac arrhythmias. In recent years it has become apparent that ion channels are part of large, multi-protein complexes, comprising not only the ion channels and their auxiliary subunits, but also components of the cytoskeleton, regulatory kinases and phosphatases, trafficking proteins, extracellular matrix proteins, and possibly even other ion channels. Disruption of any member of a particular ion channel complex has the potential to disrupt the function of the associated channels, resulting in paroxysmal disease. Understanding the molecular composition of individual ion channel signaling complexes in heart may yield important insights into the molecular basis of cardiac arrhythmias and may suggest novel therapeutic approaches to treatment of these life-threatening conditions. (C) 2005 European Society of Cardiology. Published by Elsevier B.V All rights reserved.
引用
收藏
页码:448 / 458
页数:11
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