摘要
Cardiac voltage-gated sodium channel NaV1.5, encoded by SCN5A, is crucial for the upstroke of action potential and excitation of cardiomyocytes. NaV1.5 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 NaV1.5 in terms of expression or function, eventually leading to NaV1.5-associated diseases such as lethal arrhythmias and cardiomyopathy.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 609733 |
| 期刊 | Frontiers in Physiology |
| 卷 | 11 |
| DOI | |
| 出版状态 | 已出版 - 17 12月 2020 |
学术指纹
探究 'Life Cycle of the Cardiac Voltage-Gated Sodium Channel NaV1.5' 的科研主题。它们共同构成独一无二的指纹。引用此
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