Casciola Maura, Feaster Tromondae K, Caiola Michael J, Keck Devin, Blinova Ksenia
Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, United States Food and Drug Administration, Silver Spring, MD, United States.
Front Physiol. 2023 Jan 9;13:1064168. doi: 10.3389/fphys.2022.1064168. eCollection 2022.
Pulsed electric field (PEF) cardiac ablation has been recently proposed as a technique to treat drug resistant atrial fibrillation by inducing cell death through irreversible electroporation (IRE). Improper PEF dosing can result in thermal damage or reversible electroporation. The lack of comprehensive and systematic studies to select PEF parameters for safe and effective IRE cardiac treatments hinders device development and regulatory decision-making. Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have been proposed as an alternative to animal models in the evaluation of cardiac electrophysiology safety. We developed a novel high-throughput assay to quantify the electric field threshold (EFT) for electroporation (acute effect) and cell death (long-term effect) in hiPSC-CMs. Monolayers of hiPSC-CMs were cultured in high-throughput format and exposed to clinically relevant biphasic PEF treatments. Electroporation and cell death areas were identified using fluorescent probes and confocal microscopy; electroporation and cell death EFTs were quantified by comparison of fluorescent images with electric field numerical simulations. Study results confirmed that PEF induces electroporation and cell death in hiPSC-CMs, dependent on the number of pulses and the amplitude, duration, and repetition frequency. In addition, PEF-induced temperature increase, absorbed dose, and total treatment time for each PEF parameter combination are reported. Upon verification of the translatability of the results presented here to models, this novel hiPSC-CM-based assay could be used as an alternative to animal or human studies and can assist in early nonclinical device development, as well as inform regulatory decision-making for cardiac ablation medical devices.
脉冲电场(PEF)心脏消融术最近被提出作为一种通过不可逆电穿孔(IRE)诱导细胞死亡来治疗耐药性心房颤动的技术。不当的PEF剂量可能导致热损伤或可逆电穿孔。缺乏全面系统的研究来选择用于安全有效的IRE心脏治疗的PEF参数,阻碍了设备开发和监管决策。在心脏电生理安全性评估中,人诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)已被提议作为动物模型的替代物。我们开发了一种新型高通量检测方法,以量化hiPSC-CMs中电穿孔(急性效应)和细胞死亡(长期效应)的电场阈值(EFT)。以高通量形式培养hiPSC-CMs单层,并使其暴露于临床相关的双相PEF治疗。使用荧光探针和共聚焦显微镜识别电穿孔和细胞死亡区域;通过将荧光图像与电场数值模拟进行比较来量化电穿孔和细胞死亡EFT。研究结果证实,PEF在hiPSC-CMs中诱导电穿孔和细胞死亡,这取决于脉冲数以及幅度、持续时间和重复频率。此外,还报告了每种PEF参数组合的PEF诱导的温度升高、吸收剂量和总治疗时间。在验证此处呈现的结果对模型的可翻译性后,这种基于hiPSC-CM的新型检测方法可作为动物或人体研究的替代方法,有助于早期非临床设备开发,并为心脏消融医疗设备的监管决策提供信息。