Expression of nestin, desmin and vimentin in intact and regenerating muscle spindles of rat hind limb skeletal muscles
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Desmin analysis MeSH
- Muscle Fibers, Skeletal chemistry MeSH
- Muscle, Skeletal chemistry transplantation ultrastructure MeSH
- Rats MeSH
- Myoblasts chemistry MeSH
- Muscle Spindles chemistry MeSH
- Nestin MeSH
- Rats, Inbred Lew MeSH
- Intermediate Filament Proteins analysis MeSH
- Nerve Tissue Proteins analysis MeSH
- Regeneration * MeSH
- Schwann Cells chemistry MeSH
- Vimentin analysis MeSH
- Hindlimb MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Desmin MeSH
- Nes protein, rat MeSH Browser
- Nestin MeSH
- Intermediate Filament Proteins MeSH
- Nerve Tissue Proteins MeSH
- Vimentin MeSH
We describe the expression and distribution patterns of nestin, desmin and vimentin in intact and regenerating muscle spindles of the rat hind limb skeletal muscles. Regeneration was induced by intramuscular isotransplantation of extensor digitorum longus (EDL) or soleus muscles from 15-day-old rats into the EDL muscle of adult female inbred Lewis rats. The host muscles with grafts were excised after 7-, 16-, 21- and 29-day survival and immunohistochemically stained. Nestin expression in intact spindles in host muscles was restricted to Schwann cells of sensory and motor nerves. In transplanted muscles, however, nestin expression was also found in regenerating "spindle fibers", 7 and 16 days after grafting. From the 21st day onwards, the regenerated spindle fibers were devoid of nestin immunoreactivity. Desmin was detected in spindle fibers at all developmental stages in regenerating as well as in intact spindles. Vimentin was expressed in cells of the outer and inner capsules of all muscle spindles and in newly formed myoblasts and myotubes of regenerating spindles 7 days after grafting. Our results show that the expression pattern of these intermediate filaments in regenerating spindle fibers corresponds to that found in regenerating extrafusal fibers, which supports our earlier suggestion that they resemble small-diameter extrafusal fibers.
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