Tanaka H, Ikeya K, Ozawa E
Division of Cell Biology, National Institute of Neuroscience, Tokyo, Japan.
Histochemistry. 1990;93(5):447-52. doi: 10.1007/BF00266399.
We examined the expression of dystrophin by immunohistochemical and immunoblot analyses in the skeletal and cardiac muscles of Xmdx/X+ heterozygous mice, which were obtained by mating male mdx mice (Xmdx/Y) with female wild type mice (X+/X+). Dystrophin was expressed on the surface membrane in both muscles, but the mode of expression was different between the two muscles. In cardiac muscle, dystrophin positive and negative cells were present in roughly equal numbers intermingled in a mosaic pattern; this was considered to reflect the random inactivation of X-chromosomes in early development. In skeletal muscle, most of the surface membrane was dystrophin positive. There were little signs of fiber necrosis or regeneration, and serum creatine kinase levels were normal. We are at present of opinion that the predominance of dystrophin-positive area in skeletal muscle is due to intracellular diffusion of dystrophin.
我们通过免疫组织化学和免疫印迹分析,检测了Xmdx/X+杂合小鼠骨骼肌和心肌中抗肌萎缩蛋白的表达。这些小鼠是通过将雄性mdx小鼠(Xmdx/Y)与雌性野生型小鼠(X+/X+)交配获得的。抗肌萎缩蛋白在两种肌肉的表面膜上均有表达,但两种肌肉中的表达模式不同。在心肌中,抗肌萎缩蛋白阳性和阴性细胞数量大致相等,呈镶嵌状混合存在;这被认为反映了早期发育过程中X染色体的随机失活。在骨骼肌中,大部分表面膜呈抗肌萎缩蛋白阳性。几乎没有纤维坏死或再生的迹象,血清肌酸激酶水平正常。我们目前认为,骨骼肌中抗肌萎缩蛋白阳性区域占优势是由于抗肌萎缩蛋白在细胞内的扩散所致。