SARCOLEMMAL INDENTATION IN CARDIOMYOPATHY WITH MENTAL-RETARDATION AND VACUOLAR MYOPATHY

被引:19
作者
MURAKAMI, N
GOTO, Y
ITOH, M
KATSUMI, Y
WADA, T
OZAWA, E
NONAKA, I
机构
[1] NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DEPT CELL BIOL,KODAIRA,TOKYO 187,JAPAN
[2] KOCHI MED SCH,DEPT PEDIAT,NANGO KU,KOCHI 783,JAPAN
[3] KOCHI MED SCH,DEPT SENILE MED,NANGO KU,KOCHI 783,JAPAN
[4] TOKYO MED & DENT UNIV,SCH MED,DEPT PEDIAT,BUNKYO KU,TOKYO 113,JAPAN
[5] HAMAMATSU ROSAI HOSP,DEPT NEUROL,HAMAMATSU,SHIZUOKA 430,JAPAN
关键词
CARDIOMYOPATHY; MENTAL RETARDATION; VACUOLAR MYOPATHY; CYTOPLASMIC MEMBRANE; BASAL LAMINA;
D O I
10.1016/0960-8966(94)00046-C
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Muscle biopsies from three patients with cardiomyopathy, mental retardation and increased serum creatine kinase levels revealed scattered fibers with tiny intracytoplasmic vacuoles containing basophilic and acid phosphatase-positive material and slightly increased amounts of PAS-positive granules. These findings are consistent with those seen in the so-called lysosomal glycogen storage disease with normal acid maltase. In addition to the vacuoles, there were occasional folds or indentations in the sarcolemma which were connected to the membrane enclosing the vacuoles. These membranes were well demonstrated histochemically by the nonspecific esterase and acetylcholinesterase stains. On electron microscopy, most of the vacuoles were bounded by membranes with basal lamina. The vacuolar membrane stained positively with antibodies raised to dystrophin, dystrophin-associated glycoproteins, laminin and type 4 collagen, and it was identical to the sarcolemma and its basal lamina. Therefore, the membrane abnormality which causes sarcolemmal folding is probably critical to understanding the pathomechanism of this disease.
引用
收藏
页码:149 / 155
页数:7
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