Transfection by Electroporation of Cancer and Primary Cells Using Nanosecond and Microsecond Electric Fields

Gene transfer into primary immune cells as well as into cell lines is essential for scientific and therapeutical applications. One of the methods used for gene transfer is electroporation (EP). EP is a method where a pulsed electric field (PEF) causes a highly transient permeability of the targeted...

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Main Authors: Eivina Radzevičiūtė (Author), Veronika Malyško-Ptašinskė (Author), Jurij Novickij (Author), Vitalij Novickij (Author), Irutė Girkontaitė (Author)
Format: Book
Published: MDPI AG, 2022-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Eivina Radzevičiūtė  |e author 
700 1 0 |a Veronika Malyško-Ptašinskė  |e author 
700 1 0 |a Jurij Novickij  |e author 
700 1 0 |a Vitalij Novickij  |e author 
700 1 0 |a Irutė Girkontaitė  |e author 
245 0 0 |a Transfection by Electroporation of Cancer and Primary Cells Using Nanosecond and Microsecond Electric Fields 
260 |b MDPI AG,   |c 2022-06-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14061239 
500 |a 1999-4923 
520 |a Gene transfer into primary immune cells as well as into cell lines is essential for scientific and therapeutical applications. One of the methods used for gene transfer is electroporation (EP). EP is a method where a pulsed electric field (PEF) causes a highly transient permeability of the targeted cell membrane. In this work, we present the electrotransfection of CHO-K1, 4T1 cell lines, and primary murine DCs with detectable protein-encoding plasmids in the sub-microsecond range. Microsecond (µs)- and nanosecond (ns)-range pulsed electric field transfection protocols were used. The efficiency of electrotransfection was evaluated using green fluorescent protein (GFP)-encoding plasmids (4.7 kbp; p-EGFP-N1) and plasmids expressing a firefly luciferase and red fluorescent protein (tdTomato) (8.5 kbp; pcDNA3.1(+)/Luc2 = tdT)). It was shown that the used nsPEFs protocol (7 kV/cm × 300 ns × 100, 1 MHz) ensured a better transfection efficiency than µsPEFs (1.2 kV/cm × 100 µs × 8, 1 Hz). Plasmid size and concentration had a strong impact on the cell transfection efficiency too. We also showed that there were no significant differences in transfection efficiency between immature and mature DCs. Finally, the nsPEF protocols were successfully applied for the stable transfection of the CHO-K1 cell line with the linearized pcDNA3.1(+)/Luc2 = tdT plasmid. The results of the study are applicable in gene therapy and DNA vaccination studies for the derivation of optimal electrotransfection conditions. 
546 |a EN 
690 |a plasmid DNA 
690 |a transfection 
690 |a electroporation 
690 |a GFP 
690 |a luciferase 
690 |a CHO-K1 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 6, p 1239 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/6/1239 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/13d3ca6e3b934037a31c99d821156cc2  |z Connect to this object online.