Regulation of endothelial cell morphogenesis by the protein kinase D (PKD)/glycogen synthase kinase 3 (GSK3)β pathway
pmid: 22855295
Regulation of endothelial cell morphogenesis by the protein kinase D (PKD)/glycogen synthase kinase 3 (GSK3)β pathway
Vascular morphogenesis is a key process for development, reproduction, and pathogenesis. Thus understanding the mechanisms of this process is of pathophysiological importance. Despite the fact that collagen I is the most abundant and potent promorphogenic molecule known, the molecular mechanisms by which this protein regulates endothelial cell tube morphogenesis are still unclear. Here we provide strong evidence that collagen I induces tube morphogenesis by inhibiting glycogen synthase kinase 3β (GSK3β). Further mechanistic studies revealed that GSK3β activity is regulated by protein kinase D (PKD). PKD inhibited GSK3β activity, which was required for collagen I-induced endothelial tube morphogenesis. We also found that GSK3β regulated trafficking of integrin α2β1 in a Rab11-dependent manner. Taken together, our studies highlight the important role of PKD in the regulation of collagen I-induced vascular morphogenesis and show that it is mediated by the modulation of GSK3β activity and integrin α2β1 trafficking.
- University System of Ohio United States
- University of Cincinnati United States
- University of Cincinnati Medical Center United States
Glycogen Synthase Kinase 3 beta, Endothelial Cells, Glycogen Synthase Kinase 3, Protein Transport, HEK293 Cells, Human Umbilical Vein Endothelial Cells, Morphogenesis, Humans, Integrin alpha2beta1, Protein Kinase C, Signal Transduction
Glycogen Synthase Kinase 3 beta, Endothelial Cells, Glycogen Synthase Kinase 3, Protein Transport, HEK293 Cells, Human Umbilical Vein Endothelial Cells, Morphogenesis, Humans, Integrin alpha2beta1, Protein Kinase C, Signal Transduction
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