Growth-associated protein (GAP-43) in terminal Schwann cells of rat Pacinian corpuscles
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- axony fyziologie MeSH
- krysa rodu Rattus MeSH
- membránové glykoproteiny biosyntéza MeSH
- nervus ischiadicus fyziologie MeSH
- novorozená zvířata MeSH
- potkani Sprague-Dawley MeSH
- protein GAP-43 MeSH
- proteiny nervové tkáně biosyntéza MeSH
- regenerace nervu MeSH
- rozdrcení nervu MeSH
- růstové látky biosyntéza MeSH
- Schwannovy buňky fyziologie MeSH
- stárnutí MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- membránové glykoproteiny MeSH
- protein GAP-43 MeSH
- proteiny nervové tkáně MeSH
- růstové látky MeSH
Growth-associated protein (GAP-43) immunoreactivity was examined in Pacinian corpuscles of intact neonatal and adult rats as well as after denervation and reinnervation in adult rats. All immature Pacinian corpuscles were GAP-43 immunoreactive (GAP-43+) in their inner cores while only 46 +/- 5.6% of the mature corpuscles exhibited GAP-43+ inner cores. The frequency of GAP-43+ inner cores increased to 90 +/- 7.2% after their permanent denervation. The expression of GAP-43 in the inner cores was reduced by contact with regrowing axons, but 38 +/- 5.3% of Pacinian corpuscles retained GAP-43+ in their inner cores following reinnervation. These results indicate that GAP-43 regulation is not confined only to axons but also involves some extra-axonal cues, and support a role for this protein in the process formation by terminal Schwann cells.
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