Publication | Open Access
Compartmentalized signaling by GPI-anchored ephrin-A5 requires the Fyn tyrosine kinase to regulate cellular adhesion
293
Citations
53
References
1999
Year
Cell AdhesionCellular PhysiologySignaling EventSignaling PathwayCell InteractionReceptor Tyrosine KinaseAutophagyCell SignalingCell TraffickingReceptor (Biochemistry)Cell BiologyCellular AdhesionGrowth ConesSignal TransductionDevelopmental BiologyCell-matrix InteractionCognate Eph ReceptorIntracellular TraffickingCellular BiochemistrySystems BiologyMedicineExtracellular MatrixFyn Tyrosine Kinase
Eph receptor tyrosine kinases and their corresponding surface-bound ligands, the ephrins, provide cues to the migration of cells and growth cones during embryonic development. Here we show that ephrin-A5, which is attached to the outer leaflet of the plasma membrane by a glycosyl-phosphatidylinositol-anchor, induces compartmentalized signaling within a caveolae-like membrane microdomain when bound to the extracellular domain of its cognate Eph receptor. The physiological response induced by this signaling event is concomitant with a change in the cellular architecture and adhesion of the ephrin-A5-expressing cells and requires the activity of the Fyn protein tyrosine kinase. This study stresses the relevance of bidirectional signaling involving the ephrins and Eph receptors during brain development.
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