1Department of Fundamentals of Electrical Engineering, Mathematics and Physics, University of Ljubljana, 2Department of Biomedical Engineering, University of Ljubljana
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Pavlin, M., Haberl, S., Reberšek, M., Miklavčič, D., Kandušer, M. Changing the Direction and Orientation of Electric Field During Electric Pulses Application Improves Plasmid Gene Transfer in vitro. J. Vis. Exp. (55), e3309, doi:10.3791/3309 (2011).
Gene electrotransfer is a physical method used to deliver genes into the cells by application of short and intense electric pulses, which cause destabilization of cell membrane, making it permeable to small molecules and allows transfer of large molecules such as DNA. It represents an alternative to viral vectors, due to its safety, efficacy and ease of application. For gene electrotransfer different electric pulse protocols are used in order to achieve maximum gene transfection, one of them is changing the electric field direction and orientation during the pulse delivery. Changing electric field direction and orientation increase the membrane area competent for DNA entry into the cell. In this video, we demonstrate the difference in gene electrotransfer efficacy when all pulses are delivered in the same direction and when pulses are delivered by changing alternatively the electric field direction and orientation. For this purpose tip with integrated electrodes and high-voltage prototype generator, which allows changing of electric field in different directions during electric pulse application, were used. Gene electrotransfer efficacy is determined 24h after pulse application as the number of cells expressing green fluorescent protein divided with the number of all cells. The results show that gene transfection is increased when the electric field orientation during electric pulse delivery is changed.
1. Cell culture, plasmid and buffer preparation for the experiment
2. Hardware equipment
Figure 1. Vertical and horizontal (a) cross section and photograph (b) of pipette tip with integrated electrodes. In the cross section grey color is used for the plastic housing and black for the electrodes. The pipette tip with integrated electrodes consists of four cylindrical rod electrodes. The electrodes are made of stainless steel; their diameter is 1.4 mm, adjacent electrodes are 1 mm apart, and opposite electrodes are 2 mm apart. The electrodes are glued into the plastic tip in parallel and their applicable length is 30 mm 2.
3. Gene electrotransfer protocol
Figure 2.Electric field protocols: (a) all pulses are delivered in the same direction, (b) pulses are delivered by changing alternatively the electric field direction and orientation.
4. Image acquisition and determination of gene electrotransfer efficacy
5. Representative results:
Figure 3.The percentage of cells expressing GFP when all pulses are delivered in the same direction and when pulses are delivered by changing alternatively the electric field direction and orientation is presented. Cells were exposed to a train of eight pulses with amplitude 225 V, duration 1 ms and repetition frequency of 1 Hz. Results were obtained by means of fluorescence microscopy. Each value in the graph represent mean of three independent experiments ± standard deviation. By changing the electric field direction and orientation the percentage of cells expressing GFP increases.
Gene electrotransfer is a versatile biotechnology technique that enables transfer of DNA into cells by means of applying short, high voltage electric pulses 3 and represents a safer alternative to viral vectors due to its safety, efficacy and ease of application. Although today gene electrotransfer is widely used to transfect all types of cells and first phase I clinical trial using this method has been reported 4, the underlying mechanisms are still not completely understood. It is known, that application of electric pulses of sufficient strength to the cell causes an increase in the transmembrane potential, which induces the membrane destabilization 5. Cell membrane permeability is increased and otherwise nonpermeant molecules enter the cell. Many parameters have been described 6-9, which influence the efficacy of gene electrotransfer, especially application of different pulse parameters were studied to enable better gene transfer 10-12. Changing the electric field direction and orientation during the pulse delivery increases the area of the permeabilized cell membrane 13 therefore increases competent area available for transfer of DNA molecules. It was shown, that the percentage of cells expressing transferred gene increases when electric field direction and orientation is changed during the application 14. For this purpose electric pulse generator, which allows application of electric pulses in different directions has to be used 1. We are using such pulse generator and pipette tip with integrated electrodes in order to demonstrate the difference in gene electrotransfer efficacy, when all pulses are delivered in the same direction or when pulses are delivered by changing alternatively the electric field direction and orientation. The percentage of cells expressing transferred GFP gene was assessed 24h after pulse application and the increase of successfully transfected cells when the pulses were delivered by changing alternatively the electric field direction and orientation (survival rate 80,8% ± std 12%) in comparison when all pulses were delivered in the same direction (survival rate 76% ± std 16,2%) was obtained.
No conflicts of interest declared.
This work was supported by the Slovenian Research Agency (project J2-9770, infrastructural center IP-0510 and program P2-0249). This video represents supplementary material for the "Electroporation-based Technologies and Treatments" scientific workshop and postgraduate course, organized by the Faculty of Electrical Engineering at the University of Ljubljana, Slovenia. Authors thank also Duša Hodžič for kindly providing plasmid DNA.
|HAM-F12||PAA Laboratories||E15-016||culture medium|
|fetal bovine serum||PAA Laboratories||A15-151|
|pEGFP-N1||Clontech Laboratories||6085-1||plasmid DNA|
|HiSpeed Plasmid Maxi Kit||Qiagen||12662|
|Na2HPO4||Merck & Co., Inc.||F640786 933|
|pipette tip||Custom Made|
|electric pulse generator||Custom Made|
|6 well plate||Techno Plastic Products||92406|
|15 ml centrifuge tube||Techno Plastic Products||91015|
|75 cm2 culture flask||Techno Plastic Products||90076|