Human induced pluripotent stem cell-derived atrial cardiomyocytes carrying an SCN5A mutation identify nitric oxide signaling as a mediator of atrial fibrillation

被引:28
作者
Hong, Liang [1 ]
Zhang, Meihong [1 ]
Ly, Olivia Thao [1 ]
Chen, Hanna [1 ]
Sridhar, Arvind [1 ]
Lambers, Erin [1 ]
Chalazan, Brandon [1 ]
Youn, Seock-Won [1 ]
Maienschein-Cline, Mark [2 ]
Feferman, Leonid [2 ]
Ong, Sang-Ging [1 ,3 ]
Wu, Joseph C. [4 ]
Rehman, Jalees [1 ,3 ]
Darbar, Dawood [1 ,3 ,5 ]
机构
[1] Dept Med, Div Cardiol, Chicago, IL 60607 USA
[2] Res Resources Ctr, Res Informat Core, Chicago, IL USA
[3] Univ Illinois, Dept Pharmacol, Chicago, IL 60607 USA
[4] Stanford Univ, Stanford Cardiovasc Inst, Sch Med, Stanford, CA USA
[5] Jesse Brown Vet Adm Med Ctr, Chicago, IL 60612 USA
来源
STEM CELL REPORTS | 2021年 / 16卷 / 06期
关键词
OF-FUNCTION MUTATION; GENE-EXPRESSION; SODIUM CURRENT; CHANNEL SCN5A; MECHANISMS; RANOLAZINE; REGULATOR; PHENOTYPE; VARIANTS;
D O I
10.1016/j.stemcr.2021.04.019
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mutations in SCN5A, encoding the cardiac sodium channel, are linked with familial atrial fibrillation (AF) but the underlying pathophysiologic mechanisms and implications for therapy remain unclear. To characterize the pathogenesis of AF-linked SCN5A mutations, we generated patient-specific induced pluripotent stem cell-derived atrial cardiomyocytes (iPSC-aCMs) from two kindreds carrying SCN5A mutations (E428K and N470K) and isogenic controls using CRISPR-Cas9 gene editing. We showed that mutant AF iPSC-aCMs exhibited spontaneous arrhythmogenic activity with beat-to-beat irregularity, prolonged action potential duration, and triggered-like beats. Single-cell recording revealed enhanced late sodium currents (I-Na,I-L) in AF iPSC-aCMs that were absent in a heterologous expression model. Gene expression profiling of AF iPSC-aCMs showed differential expression of the nitric oxide (NO)-mediated signaling pathway underlying enhanced I-Na,I-L. We showed that patient-specific AF iPSC-aCMs exhibited striking in vitro electrophysiological phenotype of AF-linked SCN5A mutations, and transcriptomic analyses supported that the NO signaling pathway modulated the I-Na,I-L and triggered AF.
引用
收藏
页码:1542 / 1554
页数:13
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