The mammalian KIR2.x inward rectifier ion channel family: expression pattern and pathophysiology

被引:55
|
作者
de Boer, T. P. [1 ]
Houtman, M. J. C. [1 ]
Compier, M. [1 ]
van der Heyden, M. A. G. [1 ]
机构
[1] UMCU, Dept Med Physiol, Div Heart & Lungs, NL-3584 CM Utrecht, Netherlands
关键词
Andersen-Tawil syndrome; barium; expression pattern; inward rectifier current; K(IR)2; x; thyrotoxic periodic paralysis; ANDERSEN-TAWIL-SYNDROME; SMOOTH-MUSCLE-CELLS; KIR2.X POTASSIUM CHANNELS; RECTIFYING K+ CURRENT; RETINAL GLIAL-CELLS; FUNCTIONAL EXPRESSION; MESSENGER-RNA; DIFFERENTIAL DISTRIBUTION; POSTNATAL-DEVELOPMENT; ATRIAL-FIBRILLATION;
D O I
10.1111/j.1748-1716.2010.02108.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Inward rectifier currents based on K(IR)2.x subunits are regarded as essential components for establishing a stable and negative resting membrane potential in many excitable cell types. Pharmacological inhibition, null mutation in mice and dominant positive and negative mutations in patients reveal some of the important functions of these channels in their native tissues. Here we review the complex mammalian expression pattern of K(IR)2.x subunits and relate these to the outcomes of functional inhibition of the resultant channels. Correlations between expression and function in muscle and bone tissue are observed, while we recognize a discrepancy between neuronal expression and function.
引用
收藏
页码:243 / 255
页数:13
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