MacQueen Luke A, Buschmann Michael D, Wertheimer Michael R
Department of Engineering Physics, Ecole Polytechnique, PO Box 6079 Station Centre-ville, Montreal, Qc Canada H3C 3A7.
Bioelectrochemistry. 2008 Apr;72(2):141-8. doi: 10.1016/j.bioelechem.2008.01.006. Epub 2008 Jan 24.
We report the use of dielectrophoresis (DEP) to position U-937 monocytes within a non-uniform electric field, prior to electroporation (EP) for gene delivery. DEP positioning and EP pulsing were both accomplished using a common set of inert planar electrodes, micro-fabricated on a glass substrate. A single-shell model of the cell's dielectric properties and finite-element modeling of the electric field distribution permitted us to predict the major features of cell positioning. The extent to which electric pulses increased the permeability of the cell membranes to fluorescent molecules and to pEGFPLuc DNA plasmids were found to depend on prior positioning. For a given set of pulse parameters, EP was either irreversible (resulting in cytolysis), reversible (leading to gene delivery), or not detectable, depending on where cells were positioned. Our results clearly demonstrate that position-dependent EP of cells in a non-uniform electric field can be controlled by DEP.
我们报告了在进行电穿孔(EP)基因递送之前,利用介电泳(DEP)将U-937单核细胞置于非均匀电场中的情况。DEP定位和EP脉冲均使用一组共同的惰性平面电极完成,这些电极是在玻璃基板上微加工而成的。细胞介电特性的单壳模型和电场分布的有限元建模使我们能够预测细胞定位的主要特征。发现电脉冲增加细胞膜对荧光分子和pEGFPLuc DNA质粒通透性的程度取决于先前的定位。对于给定的一组脉冲参数,根据细胞所处位置,EP要么是不可逆的(导致细胞溶解),要么是可逆的(导致基因递送),要么无法检测到。我们的结果清楚地表明,非均匀电场中细胞的位置依赖性EP可通过DEP来控制。