Rols Marie-Pierre
Institut de Pharmacologie et de Biologie Structurale, Toulouse, France.
Methods Mol Biol. 2008;423:19-33. doi: 10.1007/978-1-59745-194-9_2.
Cell membranes can be transiently permeabilized under application of electric pulses that allow hydrophilic therapeutic molecules, such as anticancer drugs and DNA, to enter into cells and tissues. This process, called electropermeabilization or electroporation, has been rapidly developed over the last decade to deliver genes to tissues and organs, but there is a general agreement that very little is known about what is really occurring during membrane electropermeabilization. It is well accepted that the entry of small molecules, such as anticancer drugs, occurs through simple diffusion while the entry of macromolecules, such as DNA, occurs through a multistep mechanism involving the electrophoretically driven association of the DNA molecule with the destabilized membrane and then its passage across the membrane. Therefore, successful DNA electrotransfer into cells depends not only on cell permeabilization but also on the way plasmid DNA interacts with the plasma membrane and, once into the cell, migrates toward the nuclei.
在施加电脉冲的情况下,细胞膜可被短暂通透化,从而使亲水性治疗分子(如抗癌药物和DNA)进入细胞和组织。这个过程称为电通透化或电穿孔,在过去十年中得到了迅速发展,用于将基因传递到组织和器官,但人们普遍认为,对于膜电通透化过程中实际发生的情况知之甚少。小分子(如抗癌药物)的进入是通过简单扩散,而大分子(如DNA)的进入则是通过一个多步骤机制,该机制涉及DNA分子通过电泳驱动与不稳定的膜结合,然后穿过膜。因此,成功地将DNA电转移到细胞中不仅取决于细胞通透化,还取决于质粒DNA与质膜相互作用的方式,以及一旦进入细胞后向细胞核迁移的方式。