Regulation of Notch1 and Dll4 by vascular endothelial growth factor in arterial endothelial cells: implications for modulating arteriogenesis and angiogenesis.

Details

Serval ID
serval:BIB_ACDC2956179C
Type
Article: article from journal or magazin.
Collection
Publications
Title
Regulation of Notch1 and Dll4 by vascular endothelial growth factor in arterial endothelial cells: implications for modulating arteriogenesis and angiogenesis.
Journal
Molecular and Cellular Biology
Author(s)
Liu Z.J., Shirakawa T., Li Y., Soma A., Oka M., Dotto G.P., Fairman R.M., Velazquez O.C., Herlyn M.
ISSN
0270-7306 (Print)
ISSN-L
0270-7306
Publication state
Published
Issued date
2003
Volume
23
Number
1
Pages
14-25
Language
english
Abstract
Notch and its ligands play critical roles in cell fate determination. Expression of Notch and ligand in vascular endothelium and defects in vascular phenotypes of targeted mutants in the Notch pathway have suggested a critical role for Notch signaling in vasculogenesis and angiogenesis. However, the angiogenic signaling that controls Notch and ligand gene expression is unknown. We show here that vascular endothelial growth factor (VEGF) but not basic fibroblast growth factor can induce gene expression of Notch1 and its ligand, Delta-like 4 (Dll4), in human arterial endothelial cells. The VEGF-induced specific signaling is mediated through VEGF receptors 1 and 2 and is transmitted via the phosphatidylinositol 3-kinase/Akt pathway but is independent of mitogen-activated protein kinase and Src tyrosine kinase. Constitutive activation of Notch signaling stabilizes network formation of endothelial cells on Matrigel and enhances formation of vessel-like structures in a three-dimensional angiogenesis model, whereas blocking Notch signaling can partially inhibit network formation. This study provides the first evidence for regulation of Notch/Delta gene expression by an angiogenic growth factor and insight into the critical role of Notch signaling in arteriogenesis and angiogenesis.
Keywords
Arteries/cytology, Arteries/physiology, Cell Division/drug effects, Cell Division/genetics, Cell Survival/drug effects, Cell Survival/genetics, Cells, Cultured, Endothelial Growth Factors/chemistry, Endothelial Growth Factors/metabolism, Endothelium, Vascular/cytology, Endothelium, Vascular/drug effects, Enzyme Inhibitors/pharmacology, Fibroblast Growth Factor 2/metabolism, Fibroblast Growth Factor 2/pharmacology, Flavonoids/pharmacology, Gene Expression Regulation, Humans, Intercellular Signaling Peptides and Proteins/chemistry, Intercellular Signaling Peptides and Proteins/metabolism, Lymphokines/chemistry, Lymphokines/metabolism, Membrane Proteins/genetics, Membrane Proteins/metabolism, Neovascularization, Physiologic, Phosphatidylinositol 3-Kinases/antagonists &amp, inhibitors, Phosphatidylinositol 3-Kinases/drug effects, Protein-Serine-Threonine Kinases, Proto-Oncogene Proteins/drug effects, Proto-Oncogene Proteins/genetics, Proto-Oncogene Proteins c-akt, Receptor, Notch1, Receptors, Cell Surface, Receptors, Notch, Recombinant Proteins/chemistry, Recombinant Proteins/genetics, Signal Transduction, Solubility, Transcription Factors, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factor Receptor-1/drug effects, Vascular Endothelial Growth Factor Receptor-1/genetics, Vascular Endothelial Growth Factor Receptor-2/drug effects, Vascular Endothelial Growth Factor Receptor-2/genetics, Vascular Endothelial Growth Factors
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 14:58
Last modification date
20/08/2019 15:16
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