钠通道
基因敲除
自噬
导航1.5
细胞生物学
化学
电生理学
脱氮酶
突变
心肌细胞
HEK 293细胞
溶酶体
调节器
内生
Brugada综合征
生物物理学
药理学
变构调节
细胞内
内科学
降级(电信)
生物
联轴节(管道)
超胸
作者
Hongbo Xiong,Di Guo,Zhen Zhou,Lilin Xiang,Xiangjie Kong,Tong Zhang,Zhijie Wang,Huanhuan Cai,Di Fan,Qiongxin Wang,Yimei Du,Qing K. Wang,Zhibing Lu,Hongbo Xiong,Di Guo,Zhen Zhou,Lilin Xiang,Xiangjie Kong,Tong Zhang,Zhijie Wang
摘要
Abstract Aims SCN5A encodes cardiac sodium channel Nav1.5 that maintains normal electrophysiological functions of hearts. Loss-of-function variants of Nav1.5 reduce sodium current densities (INa) and cause arrhythmias such as cardiac conduction block or Brugada syndrome. The regulatory mechanisms of Nav1.5 functions are not fully understood. The aim of this study was to identify novel proteins that interact with Nav1.5 and characterize their regulatory mechanisms on Nav1.5 and arrhythmias. Methods and results GST pull-down coupled with mass spectrometry, co-immunoprecipitation, and mutational analysis were used to identify de-ubiquitinating enzyme USP10 as a novel Nav1.5-interacting protein, and showed that USP10 reduces Nav1.5 protein expression and INa densities in vitro. AAV9-mediated cardiac overexpression of USP10 in mice reduced Nav1.5 protein expression, INa and ICa-L densities, shortened APD, and caused delayed ventricular activation, spontaneous atrioventricular conduction block, sinus pause, and ventricular tachycardia induced with electrical pacing. Cardiac knockdown of USP10 in Scn5a+/− mice restored Nav1.5, INa, and ICa-L to levels comparable to wild-type mice, and alleviated the conduction delay and premature ventricular contractions. Mechanistically, USP10 increased Nav1.5 protein degradation through chaperone-mediated autophagy (CMA) as the effect was blocked by lysosome inhibitor CQ and inhibition of CMA using siRNA targeting LAMP2A or HSC70, but not by proteasomal inhibitor MG132. Mutational analysis identified the key CMA degradation motif of Nav1.5 as EKRFQ431–435. USP10 decreased Nav1.5 ubiquitination and increased binding of Nav1.5 to HSC70. Mutational analysis identified K430 of Nav1.5 as the USP10 de-ubiquitination site, and K430R mutation blocked regulation of Nav1.5 by USP10. Conclusion We identified a novel CMA-mediated pathway regulating degradation of Nav1.5 by coupling with USP10-mediated de-ubiquitination at K430 of Nav1.5, which resulted in reduced INa densities and cardiac conduction defects. Knockdown of USP10 alleviated arrhythmias in Scn5a+/− mice, providing a novel therapeutic strategy for treating arrhythmias with reduced INa.
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