PI-3 kinase activity is required for epithelial-mesenchymal transformation during palate fusion

Developmental Dynamics : an Official Publication of the American Association of Anatomists
P Kang, K K H Svoboda

Abstract

Epithelial-mesenchymal transformation (EMT) is the primary mechanism for the disappearance of medial edge epithelia (MEE) during palate fusion. This phenotype transition is highly regulated by growth factors, extracellular matrix, cell surface receptors, and a variety of intracellular signaling. Phosphatidylinositol-3 (PI-3) kinase regulates cytoskeleton reorganization, cell migration, and transforming growth factor (TGF) beta-regulated EMT. Therefore, we investigated the role of PI-3 kinase in EMT during palatal fusion in vitro. Palatal shelves from embryonic (E) 13.5 day mouse embryos were collected and cultured for up to 72 hr. A specific PI-3 kinase inhibitor, LY294002, was added to the medium at concentrations of 100 etaM, 1 microM, and 10 microM. The fate of midline epithelia was traced by carboxyfluorescence labeling and analyzed by confocal microscopy. Harvested tissues were also processed for immunohistochemical analysis of a specific marker for basal lamina (laminin). Palatal fusion stages were scored on a scale of 1 to 5, with 1 equal to complete nonfusion and 5 equal to complete fusion. The mean fusion score (MFS) was calculated for each treatment group. Palatal shelves fused after 72 hr of culture in control and 10...Continue Reading

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Related Concepts

Embryo
Recombinant Transforming Growth Factor
Phosphatidylinositols
Structure of Papilla Incisiva of Mouth
Phosphatidylinositol 3-Kinases
Protoplasm
Extracellular Matrix
Receptors, Cell Surface
Mesothelium
Epithelial to Mesenchymal Transition

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