Density enhanced phosphatase-1 down-regulates urokinase receptor surface expression in confluent endothelial cells

Patrick M. Brunner, Patricia C. Heier, Judit Mihaly-Bison, Ute Priglinger, Bernd R. Binder, Gerald W. Prager

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

VEGF165, the major angiogenic growth factor, is known to activate various steps in proangiogenic endothelial cell behavior, such as endothelial cell migration and invasion, or endothelial cell survival. Thereby, the urokinase-type plasminogen activator (uPA) system has been shown to play an essential role not only by its proteolytic capacities, but also by induction of intracellular signal transduction. Therefore, expression of its cell surface receptor uPAR is thought to be an essential regulatory mechanism in angiogenesis. We found that uPAR expression on the surface of confluent endothelial cells was down-regulated compared with subconfluent proliferating endothelial cells. Regulation of uPAR expression was most probably affected by extracellular signalregulated kinase 1/2 (ERK1/2) activation, a downstream signaling event of the VEGF/VEGF-receptor system. Consistently, the receptor-like protein tyrosine phosphatase DEP-1 (density enhanced phosphatase-1/CD148), which is abundantly expressed in confluent endothelial cells, inhibited the VEGF-dependent activation of ERK1/2, leading to downregulation of uPAR expression. Overexpression of active ERK1 rescued the DEP-1 effect on uPAR. That DEP-1 plays a biologic role in angiogenic endothelial cell behavior was demonstrated in endothelial cell migration, proliferation, and capillary-like tube formation assays in vitro.

Original languageEnglish
Pages (from-to)4154-4161
Number of pages8
JournalBlood
Volume117
Issue number15
DOIs
StatePublished - 14 Apr 2011
Externally publishedYes

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