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Human in vitro assay for irreversible electroporation cardiac ablation
Introduction: 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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869257/ https://www.ncbi.nlm.nih.gov/pubmed/36699682 http://dx.doi.org/10.3389/fphys.2022.1064168 |
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author | Casciola, Maura Feaster, Tromondae K. Caiola, Michael J. Keck, Devin Blinova, Ksenia |
author_facet | Casciola, Maura Feaster, Tromondae K. Caiola, Michael J. Keck, Devin Blinova, Ksenia |
author_sort | Casciola, Maura |
collection | PubMed |
description | Introduction: 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. Methods: We developed a novel high-throughput in vitro 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. Results: 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. Discussion: Upon verification of the translatability of the in vitro results presented here to in vivo 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. |
format | Online Article Text |
id | pubmed-9869257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98692572023-01-24 Human in vitro assay for irreversible electroporation cardiac ablation Casciola, Maura Feaster, Tromondae K. Caiola, Michael J. Keck, Devin Blinova, Ksenia Front Physiol Physiology Introduction: 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. Methods: We developed a novel high-throughput in vitro 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. Results: 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. Discussion: Upon verification of the translatability of the in vitro results presented here to in vivo 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. Frontiers Media S.A. 2023-01-09 /pmc/articles/PMC9869257/ /pubmed/36699682 http://dx.doi.org/10.3389/fphys.2022.1064168 Text en Copyright © 2023 Casciola, Feaster, Caiola, Keck and Blinova. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Casciola, Maura Feaster, Tromondae K. Caiola, Michael J. Keck, Devin Blinova, Ksenia Human in vitro assay for irreversible electroporation cardiac ablation |
title | Human in vitro assay for irreversible electroporation cardiac ablation |
title_full | Human in vitro assay for irreversible electroporation cardiac ablation |
title_fullStr | Human in vitro assay for irreversible electroporation cardiac ablation |
title_full_unstemmed | Human in vitro assay for irreversible electroporation cardiac ablation |
title_short | Human in vitro assay for irreversible electroporation cardiac ablation |
title_sort | human in vitro assay for irreversible electroporation cardiac ablation |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869257/ https://www.ncbi.nlm.nih.gov/pubmed/36699682 http://dx.doi.org/10.3389/fphys.2022.1064168 |
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