Structure and function of splice variants of the cardiac voltage-gated sodium channel Nav1.5

被引:53
作者
Schroeter, Annett [1 ]
Walzik, Stefan [1 ]
Blechschmidt, Steve [1 ]
Haufe, Volker [1 ]
Benndorf, Klaus [1 ]
Zimmer, Thomas [1 ]
机构
[1] Univ Jena, Inst Physiol 2, Univ Clin, D-07743 Jena, Germany
关键词
Sodium channel; SCN5A; Cellular electrophysiology; Arrhythmias; Alternative splicing; SMOOTH-MUSCLE CELLS; DORSAL-ROOT GANGLIA; ALPHA-SUBUNIT GENES; BREAST-CANCER CELLS; NA+ CHANNEL; MESSENGER-RNA; RAT-BRAIN; SKELETAL-MUSCLE; LUNG-CANCER; MOUSE HEART;
D O I
10.1016/j.yjmcc.2010.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Voltage-gated sodium channels mediate the rapid upstroke of the action potential in excitable tissues The tetrodotoxin (TTX) resistant isoform Na(v)1.5, encoded by the SCN5A gene, is the predominant isoform in the heart. This channel plays a key role for excitability of atrial and ventricular cardiomyocytes and for rapid Impulse propagation through the specific conduction system During recent years, strong evidence has been accumulated in support of the expression of several Na(v)1.5 splice variants in the heart, and in various other tissues and cell lines including brain, dorsal root ganglia, breast cancer cells and neuronal stem cell lines This review summarizes our knowledge on the structure and putative function of nine Na(v)1.5 splice variants detected so far. Attention will be paid to the distinct biophysical properties of the four functional splice variants, to the pronounced tissue- and species-specific expression, and to the developmental regulation of Na(v)1.5 splicing The implications of alternative splicing for SCN5A channelopathies, and for a better understanding of genotype-phenotype correlations, are discussed (C) 2010 Elsevier Ltd. All rights reserved
引用
收藏
页码:16 / 24
页数:9
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