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低频刺激下兔快肌纤维的转化与替代

Fiber transformation and replacement in low-frequency stimulated rabbit fast-twitch muscles.

作者信息

Schuler M, Pette D

机构信息

Fakultät für Biologie, Universität Konstanz, Postfach 5560-M641, D-78434 Konstanz, Germany.

出版信息

Cell Tissue Res. 1996 Aug;285(2):297-303. doi: 10.1007/s004410050647.

DOI:10.1007/s004410050647
PMID:8766166
Abstract

The fast-to-slow conversion of rabbit skeletal muscles by chronic low-frequency (10 Hz, 12 h daily) stimulation involves (1) sequential fast-to-slow fiber-type transitions in the order of type IID-->type IIA-->type I, and (2) the replacement of deteriorating fast-twitch glycolytic fibers by new fibers derived from satellite cells and myotubes. These two processes were analyzed in 30- and 60-day stimulated extensor digitorum longus and tibialis anterior muscles. Fast-to-slow transforming fibers were identified by myofibrillar actomyosin histochemistry as type C fibers and immunohistochemically by their reaction with monoclonal antibodies specific to slow and fast myosin heavy chain isoforms. In situ hybridization of mRNA specific to the myosin heavy chain I isoform identified all fibers expressing slow myosin, i.e., type I and C fibers. The fraction of transforming fibers ranged between 35% and 50% in 30-day stimulated muscles. The percentage of type I fibers (20%) was threefold elevated in extensor digitorum longus muscle, but unaltered (3.5%) in tibialis anterior muscle, suggesting that fast-to-slow fiber conversion was more advanced in the former than in the latter. Fiber replacement was indicated by the finding that the fiber populations of both muscles contained 15% myotubes or small fibers with central nuclei. In situ hybridization revealed that myotubes and small regenerating fibers uniformly expressed myosin heavy chain I mRNA. Similarly, high percentages of slow-myosin-expressing myotubes and small fibers were found in 60-day stimulated muscles.

摘要

通过慢性低频(10赫兹,每天12小时)刺激使兔骨骼肌由快肌向慢肌转变,这一过程涉及:(1)纤维类型按IID型→IIA型→I型的顺序依次从快肌向慢肌转变;(2)退化的快肌糖酵解纤维被源自卫星细胞和肌管的新纤维所替代。在受刺激30天和60天的趾长伸肌和胫骨前肌中分析了这两个过程。通过肌原纤维肌动球蛋白组织化学将快肌向慢肌转变的纤维鉴定为C型纤维,并通过其与慢肌和快肌肌球蛋白重链亚型特异性单克隆抗体的反应进行免疫组织化学鉴定。对肌球蛋白重链I亚型特异性mRNA进行原位杂交,可鉴定出所有表达慢肌球蛋白的纤维,即I型和C型纤维。在受刺激30天的肌肉中,转变纤维的比例在35%至50%之间。I型纤维的百分比(20%)在趾长伸肌中升高了三倍,但在胫骨前肌中未改变(3.5%),这表明快肌向慢肌的纤维转变在前一种肌肉中比后一种肌肉中更显著。纤维替代可通过以下发现表明:两种肌肉的纤维群体中均含有15%的肌管或具有中央核的小纤维。原位杂交显示,肌管和小的再生纤维均表达肌球蛋白重链I mRNA。同样,在受刺激60天的肌肉中发现了高比例表达慢肌球蛋白的肌管和小纤维。

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