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Scalable Electrophysiological Investigation of iPS Cell-Derived Cardiomyocytes Obtained by a Lentiviral Purification Strategy

机译:慢病毒纯化策略获得的iPS细胞衍生心肌细胞的可扩展电生理学研究

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摘要

Disease-specific induced pluripotent stem (iPS) cells can be generated from patients and differentiated into functional cardiomyocytes for characterization of the disease and for drug screening. In order to obtain pure cardiomyocytes for automated electrophysiological investigation, we here report a novel non-clonal purification strategy by using lentiviral gene transfer of a puromycin resistance gene under the control of a cardiac-specific promoter. We have applied this method to our previous reported wild-type and long QT syndrome 3 (LQTS 3)-specific mouse iPS cells and obtained a pure cardiomyocyte population. These cells were investigated by action potential analysis with manual and automatic planar patch clamp technologies, as well as by recording extracellular field potentials using a microelectrode array system. Action potentials and field potentials showed the characteristic prolongation at low heart rates in LQTS 3-specific, but not in wild-type iPS cell-derived cardiomyocytes. Hence, LQTS 3-specific cardiomyocytes can be purified from iPS cells with a lentiviral strategy, maintain the hallmarks of the LQTS 3 disease and can be used for automated electrophysiological characterization and drug screening.
机译:可以从患者中产生疾病特异性的诱导多能干(iPS)细胞,并将其分化为功能性心肌细胞,以表征疾病和进行药物筛选。为了获得用于自动电生理研究的纯心肌细胞,我们在这里报告了一种新的非克隆纯化策略,通过在心脏特异性启动子的控制下使用嘌呤霉素抗性基因的慢病毒基因转移。我们已经将该方法应用于我们先前报道的野生型和长QT综合征3(LQTS 3)特异性的小鼠iPS细胞,并获得了纯的心肌细胞群。通过使用手动和自动平面膜片钳技术进行动作电位分析以及使用微电极阵列系统记录细胞外场电位来研究这些细胞。动作电位和场电位显示了LQTS 3特异性低心率时的特征性延长,而野生型iPS细胞衍生的心肌细胞中则没有。因此,可以通过慢病毒策略从iPS细胞中纯化LQTS 3特异性心肌细胞,保持LQTS 3疾病的特征,并可以用于自动电生理学表征和药物筛选。

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