The Endothelial Transcription Factor ERG Promotes Vascular Stability and Growth through Wnt/β-Catenin Signaling

Autor: Neil Dufton, Kairbaan Hodivala-Dilke, Louise E. Reynolds, Samia Taufiq Khan, Berthold Göttgens, Ralf H. Adams, Anna M. Randi, Aarti V. Shah, Holger Gerhardt, Irene M. Aspalter, Lourdes Osuna Almagro, Graeme M. Birdsey, Elisabetta Dejana, Justin C. Mason, Youwen Yang
Přispěvatelé: British Heart Foundation, Gottgens, Berthold [0000-0001-6302-5705], Apollo - University of Cambridge Repository
Jazyk: angličtina
Předmět:
Vascular Endothelial Growth Factor A
Frizzled
genetic structures
Angiogenesis
CELL DIFFERENTIATION
PATHWAY
ACTIVATION
Mice
0302 clinical medicine
Pregnancy
Lung
IN-VIVO
Cells
Cultured

beta Catenin
11 Medical and Health Sciences
Transcriptional Regulator ERG
Oncogene Proteins
0303 health sciences
biology
Wnt signaling pathway
Cadherins
3. Good health
Vascular endothelial growth factor B
Vascular endothelial growth factor A
N-CADHERIN
030220 oncology & carcinogenesis
Female
Erg
Life Sciences & Biomedicine
Signal Transduction
EXPRESSION
Chromatin Immunoprecipitation
Beta-catenin
PATHOLOGICAL ANGIOGENESIS
Blotting
Western

VE-CADHERIN
Neovascularization
Physiologic

Mice
Transgenic

Real-Time Polymerase Chain Reaction
Article
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
Antigens
CD

Human Umbilical Vein Endothelial Cells
Animals
Humans
Molecular Biology
030304 developmental biology
Science & Technology
Integrases
Cell Biology
06 Biological Sciences
GENE
Frizzled Receptors
eye diseases
Wnt Proteins
biology.protein
Cancer research
THERAPEUTIC ANGIOGENESIS
Endothelium
Vascular

sense organs
Developmental Biology
Transcription Factors
Zdroj: Developmental Cell
ISSN: 1534-5807
DOI: 10.1016/j.devcel.2014.11.016
Popis: Summary Blood vessel stability is essential for embryonic development; in the adult, many diseases are associated with loss of vascular integrity. The ETS transcription factor ERG drives expression of VE-cadherin and controls junctional integrity. We show that constitutive endothelial deletion of ERG (ErgcEC-KO) in mice causes embryonic lethality with vascular defects. Inducible endothelial deletion of ERG (ErgiEC-KO) results in defective physiological and pathological angiogenesis in the postnatal retina and tumors, with decreased vascular stability. ERG controls the Wnt/β-catenin pathway by promoting β-catenin stability, through signals mediated by VE-cadherin and the Wnt receptor Frizzled-4. Wnt signaling is decreased in ERG-deficient endothelial cells; activation of Wnt signaling with lithium chloride, which stabilizes β-catenin levels, corrects vascular defects in ErgcEC-KO embryos. Finally, overexpression of ERG in vivo reduces permeability and increases stability of VEGF-induced blood vessels. These data demonstrate that ERG is an essential regulator of angiogenesis and vascular stability through Wnt signaling.
Graphical Abstract
Highlights • Inducible deletion of endothelial ERG in mice causes defective angiogenesis • ERG controls vascular stability through Wnt/β-catenin signaling • β-catenin activation rescues the angiogenic defect in vivo in ERG-deficient mice • Overexpression of ERG in vivo stabilizes VEGF-induced angiogenesis
Birdsey, Shah et al. show that the endothelial ETS factor ERG controls Wnt/β-catenin signaling by promoting β-catenin stability, through pathways mediated by VE-cadherin and the Wnt receptor Frizzled-4. In vivo, ERG overexpression stabilizes VEGF-dependent angiogenesis. Thus, ERG is an essential regulator of angiogenesis and vascular stability through Wnt signaling.
Databáze: OpenAIRE