Danko I, Chapman V, Wolff J A
Department of Pediatrics, Waisman Center, University of Wisconsin, Madison 53705.
Pediatr Res. 1992 Jul;32(1):128-31. doi: 10.1203/00006450-199207000-00025.
The mdx mouse has been used for the development of cellular and gene therapies for Duchenne muscular dystrophy. The relatively frequent occurrence of dystrophin-positive muscle cells called revertants has hampered these efforts by interfering with data interpretation. The mdx4cv and mdx5cv dystrophin mouse mutants have approximately 10-fold fewer revertants than the mdx mutant at both 2 and 6 mo. The mdx3cv dystrophin mouse mutant may be a useful model for some types of human dystrophin deficiencies in which the levels of dystrophin are low but not completely absent.
mdx小鼠已被用于杜氏肌营养不良症细胞和基因疗法的研发。一种称为回复体的抗肌萎缩蛋白阳性肌细胞相对频繁地出现,干扰了数据解读,阻碍了这些研究工作。mdx4cv和mdx5cv抗肌萎缩蛋白小鼠突变体在2个月和6个月时的回复体数量比mdx突变体少约10倍。mdx3cv抗肌萎缩蛋白小鼠突变体可能是某些类型人类抗肌萎缩蛋白缺陷的有用模型,这些类型中抗肌萎缩蛋白水平较低但并非完全缺失。