Dean D A, Strong D D, Zimmer W E
Division of Pulmonary and Critical Care Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Gene Ther. 2005 Jun;12(11):881-90. doi: 10.1038/sj.gt.3302534.
Nonviral gene delivery is limited to a large extent by multiple extracellular and intracellular barriers. One of the major barriers, especially in nondividing cells, is the nuclear envelope. Once in the cytoplasm, plasmids must make their way into the nucleus in order to be expressed. Numerous studies have demonstrated that transfections work best in dividing populations of cells in which the nuclear envelope disassembles during mitosis, thus largely eliminating the barrier. However, since many of the cells that are targets for gene therapy do not actively undergo cell division during the gene transfer process, the mechanisms of nuclear transport of plasmids in nondividing cells are of critical importance. In this review, we summarize recent studies designed to elucidate the mechanisms of plasmid nuclear import in nondividing cells and discuss approaches to either exploit or circumvent these processes to increase the efficiency of gene transfer and therapy.
非病毒基因递送在很大程度上受到多种细胞外和细胞内屏障的限制。主要屏障之一,尤其是在非分裂细胞中,是核膜。一旦进入细胞质,质粒必须进入细胞核才能表达。大量研究表明,转染在分裂细胞群体中效果最佳,在有丝分裂期间核膜会解体,从而在很大程度上消除了这一屏障。然而,由于许多作为基因治疗靶点的细胞在基因转移过程中并不活跃地进行细胞分裂,因此质粒在非分裂细胞中的核运输机制至关重要。在这篇综述中,我们总结了旨在阐明非分裂细胞中质粒核输入机制的最新研究,并讨论利用或规避这些过程以提高基因转移和治疗效率的方法。