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PTP1b Is a Physiologic Regulator of Vascular Endothelial Growth Factor Signaling in Endothelial Cells
Author(s) -
Anthony A. Lanahan,
Diana Lech,
Alexandre Dubrac,
Jiasheng Zhang,
Zhen W. Zhuang,
Anne Eichmann,
Michael Simons
Publication year - 2014
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.114.009683
Subject(s) - angiogenesis , arteriogenesis , vascular endothelial growth factor , microbiology and biotechnology , medicine , vascular endothelial growth factor b , vascular endothelial growth factor c , regulator , matrigel , kinase insert domain receptor , conditional gene knockout , signal transduction , endothelial stem cell , vascular endothelial growth factor a , knockout mouse , biology , cancer research , receptor , in vitro , vegf receptors , biochemistry , phenotype , gene
Regulation of vascular endothelial growth factor receptor-2 (VEGFR2) signaling is a control point that determines the extent of vascular tree formation. Recent studies demonstrated an important role played by VEGFR2 endothelial trafficking in control of its activity and suggested the involvement of a phosphotyrosine phosphatase 1b (PTP1b) in this process. This study was designed to define the role of PTP1b in endothelial VEGFR2 signaling and its role in regulation of angiogenesis and arteriogenesis.

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