Holland P C, Cates G A, Wenger B S, Raney B L
Can J Biochem. 1980 Oct;58(10):1156-64. doi: 10.1139/o80-155.
Plasma membranes were prepared from primary cell cultures of normal and genetically dystrophic chick embryonic pectoral muscle. These membranes were analyzed both by one-dimensional sodium dodecyl sulphate-polyacrylamide slab gel electrophoresis and by two-dimensional electrophoresis using isoelectric focusing in the first dimension. No marked and reproducible abnormalities could be detected in the synthesis, or accumulation, of plasma membrane proteins of dystrophic muscle cells maintained in culture for periods of up to 6 days. Analysis of the relative rates of protein turnover, analysis of fucose incorporation into plasma membrane proteins, and comparison of iodinated cell surface proteins also failed to reveal distinct abnormalities in plasma membranes derived from cultured dystrophic muscle cells. Although the results obtained do not rule out an early defect in plasma membrane protein biosynthesis during the development of dystrophic skeletal muscle in vivo, they do demonstrate that the synthesis and assembly of at least the major plasma membrane proteins occur normally during the initial phases of terminal differentiation of isolated dystrophic skeletal muscle cells in tissue culture.
从正常和遗传性营养不良的鸡胚胸肌原代细胞培养物中制备质膜。通过一维十二烷基硫酸钠-聚丙烯酰胺平板凝胶电泳以及在第一维使用等电聚焦的二维电泳对这些质膜进行分析。在培养长达6天的营养不良性肌细胞的质膜蛋白合成或积累方面,未检测到明显且可重复的异常。对蛋白质周转相对速率的分析、对岩藻糖掺入质膜蛋白的分析以及对碘化细胞表面蛋白的比较,也未能揭示源自培养的营养不良性肌细胞的质膜存在明显异常。尽管所获得的结果不能排除体内营养不良性骨骼肌发育过程中质膜蛋白生物合成早期存在缺陷,但它们确实表明,在组织培养中分离的营养不良性骨骼肌细胞终末分化的初始阶段,至少主要质膜蛋白的合成和组装是正常发生的。