Differentiation of original and regenerated skeletal muscle fibres in mdx dystrophic muscles.

Abstract

The differentiation of both original muscle fibres and the regenerated muscle fibres following necrosis in mdx muscles was investigated using immunoblotting and immunocytochemical procedures. Before the onset of necrosis, postnatal skeletal muscles in mdx mouse differentiated well with only a slight delay in differentiation indicated by the level of developmental isoforms of troponin T. Prior to the onset of apparent myopathic change, both fast and slow skeletal muscle fibre types in mdx leg muscles also differentiated well when investigated by analysis of specific myosin heavy chain expression pattern. While the original muscle fibres in mdx leg muscles developed well, the differentiation of regenerated myotubes into both slow and distinct fast muscle fibre types, however, was markedly delayed or inhibited as indicated by several clusters of homogeneously staining fibres even at 14 weeks of age. The number of slow myosin heavy chain-positive myotubes amongst the regenerated muscle clusters was quite small even in soleus. This study thus established that while muscle fibres initially develop normally with only a slight delay in the differentiation process, the differentiation of regenerated myotubes in mdx muscles is markedly compromised and consequently delayed.

• Authors: John C Earnshaw, Phillip Kyprianou, Kewal Krishan, Gurtej K Dhoot
• Journal: Histochemistry and cell biology (Histochem Cell Biol) Vol. 118 Issue 1 Pg. 19-27 (Jul 2002) ISSN: 0948-6143 [Print] Germany
• PMID: 12122443 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Protein Isoforms
• Troponin T
• Myosin Heavy Chains

Topics

• Animals
• Mice
• Mice, Inbred mdx
• Muscle Development
• Muscle Fibers, Fast-Twitch (chemistry, pathology, physiology)
• Muscle Fibers, Skeletal (chemistry, pathology, physiology)
• Muscle Fibers, Slow-Twitch (chemistry, pathology, physiology)
• Muscle, Skeletal (pathology, physiology)
• Muscular Dystrophy, Animal (pathology, physiopathology)
• Myosin Heavy Chains (analysis)
• Protein Isoforms (analysis)
• Regeneration
• Troponin T (analysis)