Life Cycle of the Cardiac Voltage-Gated Sodium Channel NaV1.5

被引:21
|
作者
Dong, Caijuan [1 ]
Wang, Ya [1 ]
Ma, Aiqun [1 ,2 ,3 ]
Wang, Tingzhong [1 ,2 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Cardiovasc Med, Xian, Peoples R China
[2] Key Lab Mol Cardiol, Xian, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Minist Educ, Key Lab Environm & Genes Related Dis, Xian, Peoples R China
来源
FRONTIERS IN PHYSIOLOGY | 2020年 / 11卷
基金
中国国家自然科学基金;
关键词
Na(V)1; 5; SCN5A; biosynthesis; trafficking; anchoring; degradation; gating modulation; post-transcriptional modification; PROTEIN-KINASE-II; BRUGADA SYNDROME; HEART-FAILURE; TRANSCRIPTIONAL REGULATION; SCN5A EXPRESSION; NA+ CURRENT; GENE SCN5A; MUTATION; IDENTIFICATION; MODULATION;
D O I
10.3389/fphys.2020.609733
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Cardiac voltage-gated sodium channel Na(V)1.5, encoded by SCN5A, is crucial for the upstroke of action potential and excitation of cardiomyocytes. Na(V)1.5 undergoes complex processes before it reaches the target membrane microdomains and performs normal functions. A variety of protein partners are needed to achieve the balance between SCN5A transcription and mRNA decay, endoplasmic reticulum retention and export, Golgi apparatus retention and export, selective anchoring and degradation, activation, and inactivation of sodium currents. Subtle alterations can impair Na(V)1.5 in terms of expression or function, eventually leading to Na(V)1.5-associated diseases such as lethal arrhythmias and cardiomyopathy.
引用
收藏
页数:11
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