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Syndecan recycling [corrected] is controlled by syntenin-PIP2 interaction and Arf6
Authors:Zimmermann Pascale  Zhang Zhe  Degeest Gisèle  Mortier Eva  Leenaerts Iris  Coomans Christien  Schulz Joachim  N'Kuli Francisca  Courtoy Pierre J  David Guido
Affiliation:Laboratory for Glycobiology and Developmental Genetics, Department of Human Genetics, University of Leuven, Belgium. pascale.zimmerman@med.kuleuven.be
Abstract:Syndecans are heparan sulfate proteoglycans that modulate the activity of several growth factors and cell adhesion molecules. PDZ domains in the adaptor protein syntenin interact with syndecans and with the phosphoinositide PIP(2), which is involved in the regulation of the actin cytoskeleton and membrane trafficking. Here, we show that the syntenin PDZ domain-PIP(2) interaction controls Arf6-mediated syndecan recycling through endosomal compartments. FGF receptor accompanies syndecan along the syntenin-mediated recycling pathway, in a heparan sulfate- and FGF-dependent manner. Syndecans that cannot recycle via this pathway become trapped intracellularly and inhibit cell spreading. This syntenin-mediated syndecan recycling pathway may regulate the surface availability of a number of cell adhesion and signaling molecules.
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