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Genetically engineered HEK cells as a valuable tool for studying electroporation in excitable cells
ID Batista Napotnik, Tina (Author), ID Kos, Bor (Author), ID Jarm, Tomaž (Author), ID Miklavčič, Damijan (Author), ID O'Connor, Rodney P. (Author), ID Rems, Lea (Author)

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Abstract
Electric pulses used in electroporation-based treatments have been shown to affect the excitability of muscle and neuronal cells. However, understanding the interplay between electroporation and electrophysiological response of excitable cells is complex, since both ion channel gating and electroporation depend on dynamic changes in the transmembrane voltage (TMV). In this study, a genetically engineered human embryonic kidney cells expressing NaV1.5 and Kir2.1, a minimal complementary channels required for excitability (named S-HEK), was characterized as a simple cell model used for studying the effects of electroporation in excitable cells. S-HEK cells and their nonexcitable counterparts (NS-HEK) were exposed to 100 µs pulses of increasing electric field strength. Changes in TMV, plasma membrane permeability, and intracellular Ca2+ were monitored with fluorescence microscopy. We found that a very mild electroporation, undetectable with the classical propidium assay but associated with a transient increase in intracellular Ca2+, can already have a profound effect on excitability close to the electrostimulation threshold, as corroborated by multiscale computational modelling. These results are of great relevance for understanding the effects of pulse delivery on cell excitability observed in context of the rapidly developing cardiac pulsed field ablation as well as other electroporation-based treatments in excitable tissues.

Language:English
Keywords:electroporation, exitable cells, action potential, intacellular calcium
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FE - Faculty of Electrical Engineering
Publication status:Published
Publication version:Version of Record
Year:2024
Number of pages:18 str.
Numbering:14, art. 720
PID:20.500.12556/RUL-171185 This link opens in a new window
UDC:602.621
ISSN on article:2045-2322
DOI:10.1038/s41598-023-51073-5 This link opens in a new window
COBISS.SI-ID:180220419 This link opens in a new window
Publication date in RUL:18.08.2025
Views:586
Downloads:217
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Record is a part of a journal

Title:Scientific reports
Shortened title:Sci. rep.
Publisher:Springer Nature
ISSN:2045-2322
COBISS.SI-ID:18727432 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:elektroporacija, vzdražne celice, akcijski potencial, znotrajcelični kalcij

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P2-0249
Name:Elektroporacija v biologiji, biotehnologiji in medicini

Funder:ARRS - Slovenian Research Agency
Project number:J2-2503
Name:Vpliv visokonapetostnih električnih pulzov na membranske proteine pri elektroporaciji

Funder:ARRS - Slovenian Research Agency
Project number:I0-0022
Name:Mreža raziskovalnih infrastrukturnih centrov Univerze v Ljubljani (MRIC UL)

Funder:Other - Other funder or multiple funders
Funding programme:Medtronic
Project number:-
Name:Medtronic

Funder:EC - European Commission
Project number:893077
Name:Controlling the susceptibility of biological cells to pulsed electric field treatment by using ion channel modulators
Acronym:EPmIC

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