Ankyrin-based cellular pathways for cardiac ion channel and transporter targeting and regulation

被引:17
|
作者
Cunha, Shane R. [1 ,2 ]
Mohler, Peter J. [1 ,2 ]
机构
[1] Univ Iowa, Dept Internal Med, Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Mol Physiol & Biophys, Carver Coll Med, Iowa City, IA 52242 USA
关键词
Ankyrin; Nav1.5; Intercalated disc; Transverse-tubule; Arrhythmia; Sodium channel; Targeting; BRAIN SODIUM-CHANNELS; C-TERMINAL DOMAIN; IDENTIFICATION; SUBUNIT; BINDING; LOCALIZATION; EXPRESSION; SURFACE; FAMILY; MOTIF;
D O I
10.1016/j.semcdb.2010.09.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The coordinate activities of ion channels and transporters regulate myocyte membrane excitability and normal cardiac function. Dysfunction in cardiac ion channel and transporter function may result in cardiac arrhythmias and sudden cardiac death. While the past fifteen years have linked defects in ion channel biophysical properties with human disease, more recent findings illustrate that ion channel and transporter localization within cardiomyocytes is equally critical for normal membrane excitability and tissue function. Ankyrins are a family of multifunctional adapter proteins required for the expression, membrane localization, and regulation of select cardiac ion channels and transporters. Notably, loss of ankyrin expression in mice, and ankyrin loss-of-function in humans is now associated with defects in myocyte excitability and cardiac physiology. Here, we provide an overview of the roles of ankyrin polypeptides in cardiac physiology, as well as review other recently identified pathways required for the membrane expression and regulation of key cardiac ion channels and transporters. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 170
页数:5
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