Kurita Hirofumi, Takao Yasuhiro, Kishikawa Kenta, Takashima Kazunori, Numano Rika, Mizuno Akira
Department of Environmental and Life Sciences, Graduate School of Engineering, Toyohashi University of Technology, 1-1 Hibarigaoka, Tempaku-cho, Toyohashi, Aichi 441-8580, Japan.
Electronics-Inspired Interdisciplinary Research Institute, Toyohashi University of Technology, 1-1 Hibarigaoka, Tempaku-cho, Toyohashi, Aichi 441-8580, Japan.
Biochem Biophys Rep. 2016 Aug 12;8:81-88. doi: 10.1016/j.bbrep.2016.08.001. eCollection 2016 Dec.
We have developed a gene transfection method called water-in-oil droplet electroporation (EP) that uses a dielectric oil and a liquid droplet containing live cells and exogenous DNA. When a cell suspension droplet is placed between a pair of electrodes, an intense DC electric field can induce droplet deformation, resulting in an instantaneous short circuit caused by the droplet elongating and contacting the two electrodes simultaneously. Small transient pores are generated in the cell membrane during the short, allowing the introduction of exogenous DNA into the cells. The droplet EP was characterized by varying the following experimental parameters: applied voltage, number of short circuits, type of medium (electric conductivity), concentration of exogenous DNA, and size of the droplet. In addition, the formation of transient pores in the cell membrane during droplet EP and the transfection efficiency were evaluated.
我们开发了一种名为油包水液滴电穿孔(EP)的基因转染方法,该方法使用介电油以及含有活细胞和外源DNA的液滴。当将细胞悬液滴置于一对电极之间时,强直流电场可诱导液滴变形,导致液滴伸长并同时接触两个电极,从而引起瞬时短路。在短路期间,细胞膜上会产生小的瞬时孔,使外源DNA得以导入细胞。通过改变以下实验参数来表征液滴电穿孔:施加电压、短路次数、培养基类型(电导率)、外源DNA浓度和液滴大小。此外,还评估了液滴电穿孔过程中细胞膜上瞬时孔的形成以及转染效率。