Interplay between Electric Field Strength and Number of Short-Duration Pulses for Efficient Gene Electrotransfer

Author:

Urbanskas Ernestas1,Jakštys Baltramiejus12ORCID,Venckus Justinas1,Malakauskaitė Paulina23,Šatkauskienė Ingrida1,Morkvėnaitė-Vilkončienė Inga4ORCID,Šatkauskas Saulius1ORCID

Affiliation:

1. Research Institute of Natural and Technological Sciences, Vytautas Magnus University, 44404 Kaunas, Lithuania

2. Faculty of Electronics, Vilnius Gediminas Technical University, 10105 Vilnius, Lithuania

3. Department of Immunology and Bioelectrochemistry, State Research Institute Centre for Innovative Medicine, 08406 Vilnius, Lithuania

4. Department of Nanotechnology, State Research Institute Centre for Physical Sciences and Technology, 02300 Vilnius, Lithuania

Abstract

Electroporation is a method that shows great promise as a non-viral approach for delivering genes by using high-voltage electric pulses to introduce DNA into cells to induce transient gene expression. This research aimed to evaluate the interplay between electric pulse intensity and 100 µs-duration pulse numbers as an outcome of gene electrotransfer efficacy and cell viability. Our results indicated a close relationship between pulse number and electric field strength regarding gene electrotransfer efficacy; higher electric pulse intensity resulted in fewer pulses needed to achieve the same gene electrotransfer efficacy. Subsequently, an increase in pulse number had a more negative impact on overall gene electrotransfer by significantly reducing cell viability. Based on our data, the best pulse parameters to transfect CHO cells with the pMax-GFP plasmid were using 5 HV square wave pulses of 1000 V/cm and 2 HV of 1600 V/cm, correspondingly resulting in 55 and 71% of transfected cells and maintaining 79 and 54% proliferating cells. This shows ESOPE-like 100 µs-duration pulse protocols can be used simultaneously to deliver cytotoxic drugs as well as immune response regulating genetically encoded cytokines.

Funder

Research Council of Lithuania

Publisher

MDPI AG

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