DEFECTIVE DEVELOPMENT OF THE CRANIOFACIAL DIGESTIVE COMPLEX OF XENOPUS-LAEVIS AFTER TREATMENT WITH ENDOGENOUS GALACTOSIDE-BINDING LECTIN ORITS HAPTEN INHIBITOR THIODIGALACTOSIDE/

Citation
Pv. Varma et al., DEFECTIVE DEVELOPMENT OF THE CRANIOFACIAL DIGESTIVE COMPLEX OF XENOPUS-LAEVIS AFTER TREATMENT WITH ENDOGENOUS GALACTOSIDE-BINDING LECTIN ORITS HAPTEN INHIBITOR THIODIGALACTOSIDE/, Journal of craniofacial genetics and developmental biology, 14(3), 1994, pp. 177-191
Citations number
40
Categorie Soggetti
Genetics & Heredity","Developmental Biology","Anatomy & Morphology
ISSN journal
02704145
Volume
14
Issue
3
Year of publication
1994
Pages
177 - 191
Database
ISI
SICI code
0270-4145(1994)14:3<177:DDOTCD>2.0.ZU;2-G
Abstract
The regions of the developing craniofacial skeleton and gut of Xenopus laevis have been confronted in vivo with purified embryonic galactosi de-binding lectin or its hapten inhibitor thiodigalactoside (TDG). Con frontation was carried out at stage 24-26 (cranial neural crest migrat ing). Further development of the head skeleton and gut has been monito red in living animals and in histological cross-sections of selected h ead regions. Lectin treatment correlates with the development of large r heads than controls. TDG treatment correlates with the development o f narrower heads than controls. After both treatments, head cartilages are composed of fewer total chondrocytes. Both neural crest and non-n eural crest cartilages are affected. The gut forms larger, irregular c oils after lectin or TDG confrontation. The results suggest that galac toside-binding lectin/galactoside-bearing receptor adhesive interactio ns are important in development of the craniofacial/visceral skeleton and gut.