Literature DB >> 6196637

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

T Miike.   

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.

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Year:  1983        PMID: 6196637     DOI: 10.1002/mus.880060802

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  5 in total

Review 1.  Mechanisms of resistance to pathogenesis in muscular dystrophies.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1999-05       Impact factor: 3.396

2.  Increased density of satellite cells in the absence of fibre degeneration in muscle of myotonic mice.

Authors:  J Schimmelpfeng; H Jockusch; P Heimann
Journal:  Cell Tissue Res       Date:  1987-08       Impact factor: 5.249

3.  Fibres of intermediate type 1C and 2C are found continuously in mdx soleus muscle up to 52 weeks.

Authors:  C Pastoret; A Sebille
Journal:  Histochemistry       Date:  1993-10

4.  Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch.

Authors:  P Moens; P H Baatsen; G Maréchal
Journal:  J Muscle Res Cell Motil       Date:  1993-08       Impact factor: 2.698

5.  Experimental serotonin myopathy as an animal model of muscle degeneration and regeneration in muscular dystrophy.

Authors:  H Narukami; K Yoshioka; J Zhao; T Miike
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

  5 in total

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