Coulton G R, Skynner M J, Smith T, Pagel C N, Partridge T A
Department of Biochemistry, Charing Cross and Westminster Medical School, London, UK.
Histochem J. 1991 Jul;23(7):323-7. doi: 10.1007/BF01044963.
The development of therapies, based upon implantation of normal muscle cell precursors, for the treatment of skeletal muscle diseases such as Duchenne Muscular Dystrophy is in its infancy. Detailed analysis of the genetic and phenotypic contribution made by donor myoblasts to the regenerated muscle is critical. Using non-radioactive in situ hybridization of a Y chromosome-specific DNA probe to sections of muscle, we have localized the position of male donor nuclei within female host muscles after myoblast implantation. These results were compared with the distribution of immunocytochemically-localized dystrophin and the expression of donor-specific glucose phosphate isomerase by isoelectric-focussing. We found consistent male-specific nuclear hybridization and a close spatial relationship between the distribution of male donor nuclei and dystrophin-positive muscle fibres within female, dystrophin-negative host muscles. This approach will be useful in the further analysis of myoblast implantation experiments.
基于植入正常肌肉细胞前体来治疗诸如杜氏肌营养不良症等骨骼肌疾病的疗法尚处于起步阶段。详细分析供体成肌细胞对再生肌肉的遗传和表型贡献至关重要。通过对肌肉切片进行Y染色体特异性DNA探针的非放射性原位杂交,我们确定了成肌细胞植入后雌性宿主肌肉中雄性供体细胞核的位置。将这些结果与免疫细胞化学定位的抗肌萎缩蛋白的分布以及通过等电聚焦检测的供体特异性葡萄糖磷酸异构酶的表达进行了比较。我们在雌性、抗肌萎缩蛋白阴性的宿主肌肉中发现了一致的雄性特异性核杂交信号,并且雄性供体细胞核的分布与抗肌萎缩蛋白阳性肌纤维之间存在密切的空间关系。这种方法将有助于进一步分析成肌细胞植入实验。