Gollins H, McMahon J, Wells K E, Wells D J
Gene Targeting Unit, Department of Neuromuscular Diseases, Division of Neuroscience and Psychological Medicine, Imperial College Faculty of Medicine, Charing Cross Hospital, London, UK.
Gene Ther. 2003 Mar;10(6):504-12. doi: 10.1038/sj.gt.3301927.
The efficiency of plasmid gene transfer in skeletal muscle is significantly enhanced by pretreatment with hyaluronidase and the application of an electrical field to the muscle following the injection of plasmid DNA, a process referred to as electrotransfer. However, the presence of increased levels of connective tissue in muscular dystrophies, such as Duchenne muscular dystrophy (DMD), may affect the efficiency of this process. Here we demonstrate that the efficiency of electrotransfer is not affected by increased levels of connective tissue in the mdx mouse model of DMD and that any damage induced by the electrotransfer process is not exacerbated in the dystrophic phenotype. However, increasing the concentration of hyaluronidase does not improve transfection efficiencies further. Unlike direct injection of plasmid DNA, the efficiency of electrotransfer is not dependent upon the sex and age of mice used. The combined treatment of hyaluronidase and electrotransfer results in highly efficient gene transfer in dystrophic muscle with limited muscle damage.
用透明质酸酶预处理以及在注射质粒 DNA 后对肌肉施加电场(该过程称为电转染)可显著提高骨骼肌中质粒基因转移的效率。然而,诸如杜氏肌营养不良症(DMD)等肌肉营养不良症中结缔组织水平的升高可能会影响这一过程的效率。在此我们证明,在 DMD 的 mdx 小鼠模型中,电转染效率不受结缔组织水平升高的影响,并且电转染过程引起的任何损伤在营养不良表型中都不会加剧。然而,增加透明质酸酶的浓度并不能进一步提高转染效率。与直接注射质粒 DNA 不同,电转染效率不依赖于所用小鼠的性别和年龄。透明质酸酶和电转染的联合处理可在营养不良肌肉中实现高效基因转移,且肌肉损伤有限。