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杜兴氏肌营养不良症和先天性肌营养不良症病例中再生肌纤维的成熟缺陷。

Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies.

作者信息

Miike T

出版信息

Muscle Nerve. 1983 Oct;6(8):545-52. doi: 10.1002/mus.880060802.

Abstract

Immature fibers in Duchenne muscular dystrophy (DMD) and congenital muscular dystrophies (CMD) were compared with human fetal muscles and experimentally-induced regenerating muscle fibers using the acridine orange (AO) technique on fluorescent microscopy and histochemical methods. Strong AO activity was observed on immature fibers in dystrophies and on experimentally-induced fibers in the early stages of regeneration. These young fibers showed type 2C histochemical reactions on ATPase stains. Human fetal muscles failed to show these fibers which were seen in the muscular dystrophies and the experimental regenerating muscle. From these results it is concluded that immature fibers in muscular dystrophies are early stages of regenerating fibers and not maturationally arrested fetal muscle fibers. In addition, these immature fibers formed small groups composed of 10 to 50 fibers in muscular dystrophies and sometimes large groups in CMD. It is suggested that the investigation of immature fibers and their grouping is quite important for revealing the pathogenesis of the muscular dystrophies.

摘要

运用吖啶橙(AO)技术,通过荧光显微镜检查和组织化学方法,将杜兴氏肌营养不良症(DMD)和先天性肌营养不良症(CMD)中的未成熟纤维与人类胎儿肌肉以及实验诱导的再生肌纤维进行了比较。在营养不良症的未成熟纤维以及再生早期的实验诱导纤维上观察到了强烈的AO活性。这些年轻纤维在ATP酶染色上呈现2C型组织化学反应。人类胎儿肌肉中未出现肌肉营养不良症和实验性再生肌肉中所见的这些纤维。从这些结果可以得出结论,肌肉营养不良症中的未成熟纤维是再生纤维的早期阶段,而非成熟停滞的胎儿肌纤维。此外,这些未成熟纤维在肌肉营养不良症中形成了由10至50根纤维组成的小群体,在CMD中有时形成大群体。有人提出,对未成熟纤维及其分组的研究对于揭示肌肉营养不良症的发病机制非常重要。

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