Morandi L, Mora M, Gussoni E, Tedeschi S, Cornelio F
Neuromuscular Diseases Department, Istituto Neurologico C. Besta, Milano, Italy.
Ann Neurol. 1990 Nov;28(5):674-9. doi: 10.1002/ana.410280512.
Immunocytochemical localization and immunoblot analysis of dystrophin in muscle fibers of 11 obligate and probable, and 7 possible carriers of Duchenne and Becker muscular dystrophy revealed an abnormal expression of the protein in 3 of them. Localization of calcium and albumin, as endogenous markers of extracellular fluid penetration, showed the presence of both molecules inside some fibers lacking dystrophin. Our morphological studies show that the initial stages leading to fiber necrosis in Duchenne muscular dystrophy are present in carriers with mosaicism. Comparison of dystrophin studies with restriction fragment length polymorphism analysis and creatine kinase levels showed that neither immunocytochemical nor immunoblot techniques for dystrophin are sensitive enough to provide a basis for genetic counseling.
对11名杜兴氏和贝克氏肌营养不良症的确诊携带者、疑似携带者以及7名可能的携带者的肌纤维进行肌营养不良蛋白的免疫细胞化学定位和免疫印迹分析,结果显示其中3人该蛋白表达异常。作为细胞外液渗透内源性标志物的钙和白蛋白的定位显示,在一些缺乏肌营养不良蛋白的纤维内部存在这两种分子。我们的形态学研究表明,杜兴氏肌营养不良症中导致纤维坏死的初始阶段存在于具有嵌合体的携带者中。将肌营养不良蛋白研究与限制性片段长度多态性分析及肌酸激酶水平进行比较,结果表明,用于肌营养不良蛋白的免疫细胞化学和免疫印迹技术都不够敏感,无法为遗传咨询提供依据。