POLYSIALYLATED NEURAL CELL-ADHESION MOLECULE AND PLASTICITY OF IPSILATERAL CONNECTIONS IN XENOPUS TECTUM

Citation
Dk. Williams et al., POLYSIALYLATED NEURAL CELL-ADHESION MOLECULE AND PLASTICITY OF IPSILATERAL CONNECTIONS IN XENOPUS TECTUM, Neuroscience, 70(1), 1996, pp. 277-285
Citations number
50
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
03064522
Volume
70
Issue
1
Year of publication
1996
Pages
277 - 285
Database
ISI
SICI code
0306-4522(1996)70:1<277:PNCMAP>2.0.ZU;2-J
Abstract
The optic tectum of Xenopus offers a readily manipulated system for te sting the hypothesis that polysialylation of the neural cell adhesion molecule is associated with axonal plasticity. Axons relaying input to the tectum from the ipsilateral eye employ visual input to establish a topographic map in register with the contralateral map, despite natu rally-occurring or surgically-induced repositioning of the eyes. This capacity for activity-dependent refinement or re-organization of the i psilateral map is normally confined to a period between about one and four months postmetamorphosis bur can be restored in adults by local a pplication of N-methyl-D aspartate to the tectum. In addition, dark-re aring prolongs plasticity indefinitely. We have used immunohistochemic al staining with antibodies to polysialic acid to determine whether co nditions of high plasticity are correlated with high levels of polysia lylated neural cell adhesion molecule in the tectum. We find that the staining level is high in tecta from one to three month postmetamorphi c frogs but is low both before and after this period. Thus, in normal Xenopus frogs, anti-polysialic acid staining is heavier in the period of high plasticity than in the preceding or following postmetamorphic periods. As a further test of this relationship, we examined brains of adults with experiment ally-induced plasticity. Tecta of N-methyl-D-a spartate-treated adults and of dark-reared adults showed higher levels of staining than did the tecta of normally-reared adults. These resul ts also support the hypothesis that the presence of high levels of pol ysialic acid on neural cell adhesion molecules is causally related to activity-related changes in axonal growth patterns.