Electrophysiologic Characterization of Calcium Handling in Human Induced Pluripotent Stem Cell-Derived Atrial Cardiomyocytes

被引:44
作者
Argenziano, Mariana [1 ,2 ]
Lambers, Erin [1 ]
Hong, Liang [1 ]
Sridhar, Arvind [1 ]
Zhang, Meihong [1 ]
Chalazan, Brandon [1 ]
Menon, Ambili [1 ]
Savio-Galimberti, Eleonora [1 ,2 ]
Wu, Joseph C. [3 ]
Rehman, Jalees [1 ,4 ]
Darbar, Dawood [1 ,4 ]
机构
[1] Univ Illinois, Div Cardiol, Dept Med, 840 S Wood St,920S MC 715, Chicago, IL 60612 USA
[2] Lankenau Inst Med Res, Wynnewood, PA USA
[3] Stanford Univ, Med Ctr, Dept Med, Div Cardiol,Stanford Cardiovasc Inst, Stanford, CA 94305 USA
[4] Univ Illinois, Dept Pharmacol, Chicago, IL 60612 USA
关键词
COUP-TFII; FIBRILLATION; CHANNEL; DIFFERENTIATION;
D O I
10.1016/j.stemcr.2018.04.005
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human induced pluripotent stem cell (hiPSC)-derived atrial cardiomyocytes (CMs) hold great promise for elucidating underlying cellular mechanisms that cause atrial fibrillation (AF). In order to use atrial-like hiPSC-CMs for arrhythmia modeling, it is essential to better understand the molecular and electrophysiological phenotype of these cells. We performed comprehensive molecular, transcriptomic, and electrophysiologic analyses of retinoic acid (RA)-guided hiPSC atrial-like CMs and demonstrate that RA results in differential expression of genes involved in calcium ion homeostasis that directly interact with an RA receptor, chicken ovalbumin upstream promoter-transcription factor 2 (COUP-TFII). We report a mechanism by which RA generates an atrial-like electrophysiologic signature through the downstream regulation of calcium channel gene expression by COUP-TFII and modulation of calcium handling. Collectively, our results provide important insights into the underlying molecular mechanisms that regulate atrial-like hiPSC-CM electrophysiology and support the use of atrial-like CMs derived from hiPSCs to model AF.
引用
收藏
页码:1867 / 1878
页数:12
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