4.7 Article

Gene Electrotransfer into Mammalian Cells Using Commercial Cell Culture Inserts with Porous Substrate

Journal

PHARMACEUTICS
Volume 14, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics14091959

Keywords

localized electroporation; gene electrotransfer; plasmid; transfection; cell culture insert; numerical modeling; Chinese hamster ovary cells; myoblasts

Funding

  1. European Union [893077, 101038051]
  2. Slovenian Research Agency (ARRS) [J2-2503, P2-0249]
  3. German Academic Exchange Service (DAAD) through the Programme for Project-Related Personal Exchange
  4. Marie Curie Actions (MSCA) [893077] Funding Source: Marie Curie Actions (MSCA)

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In this study, a localized electroporation method based on commercially available cell culture inserts and porous substrates was designed to enhance gene electrotransfer efficiency while preserving cell viability. The device tested in mammalian cell lines showed similar transfection efficiencies to conventional bulk electroporation, but with lower voltage pulses and without the need for expensive electroporators.
Gene electrotransfer is one of the main non-viral methods for intracellular delivery of plasmid DNA, wherein pulsed electric fields are used to transiently permeabilize the cell membrane, allowing enhanced transmembrane transport. By localizing the electric field over small portions of the cell membrane using nanostructured substrates, it is possible to increase considerably the gene electrotransfer efficiency while preserving cell viability. In this study, we expand the frontier of localized electroporation by designing an electrotransfer approach based on commercially available cell culture inserts with polyethylene-terephthalate (PET) porous substrate. We first use multiscale numerical modeling to determine the pulse parameters, substrate pore size, and other factors that are expected to result in successful gene electrotransfer. Based on the numerical results, we design a simple device combining an insert with substrate containing pores with 0.4 mu m or 1.0 mu m diameter, a multiwell plate, and a pair of wire electrodes. We test the device in three mammalian cell lines and obtain transfection efficiencies similar to those achieved with conventional bulk electroporation, but at better cell viability and with low-voltage pulses that do not require the use of expensive electroporators. Our combined theoretical and experimental analysis calls for further systematic studies that will investigate the influence of substrate pore size and porosity on gene electrotransfer efficiency and cell viability.

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