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J Pediatr Surg ; 45(10): 2030-5, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20920724

ABSTRACT

BACKGROUND/PURPOSE: The Fgf10 signaling pathway plays an important role in early stages of mouse embryonic palatal development, which is associated with cell proliferation and differentiation. The objective of this study was to assess whether dexamethasone and vitamin B(12) affected the Fgf10 signal pathway of mouse embryonic palate. MATERIALS AND METHODS: Immunohistochemical studies were performed for expression of Fgf10, Fgfr2b, and sonic hedgehog and for cell proliferation and apoptosis of mouse embryonic palate. RESULTS: The expression of Fgf10, Fgfr2b, and sonic hedgehog was changed in mouse embryonic palate after dexamethasone and vitamin B(12) treatment, resulting in reduced and restored proliferation of mesenchymal cells. CONCLUSIONS: Dexamethasone and vitamin B(12) affected the Fgf10 signaling pathway and cell proliferation of mouse embryonic palate. Cell apoptosis was not altered after dexamethasone and vitamin B(12) exposure.


Subject(s)
Cleft Palate/embryology , Dexamethasone/pharmacology , Fibroblast Growth Factor 10/genetics , Glucocorticoids/pharmacology , Animals , Apoptosis/drug effects , Apoptosis/genetics , Cell Proliferation/drug effects , Cleft Palate/physiopathology , Disease Models, Animal , Embryonic Development/drug effects , Embryonic Development/genetics , Female , Fibroblast Growth Factor 10/drug effects , Gene Expression Regulation, Developmental/drug effects , Gene Expression Regulation, Developmental/genetics , Male , Mice , Mice, Inbred C57BL , Palate/drug effects , Palate/embryology , Receptor, Fibroblast Growth Factor, Type 1/drug effects , Receptor, Fibroblast Growth Factor, Type 1/genetics , Signal Transduction/drug effects , Signal Transduction/genetics , Vitamin B 12/pharmacology
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