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Complex Formation between VEGFR2 and the β 2 -Adrenoceptor.

Authors :
Kilpatrick LE
Alcobia DC
White CW
Peach CJ
Glenn JR
Zimmerman K
Kondrashov A
Pfleger KDG
Ohana RF
Robers MB
Wood KV
Sloan EK
Woolard J
Hill SJ
Source :
Cell chemical biology [Cell Chem Biol] 2019 Jun 20; Vol. 26 (6), pp. 830-841.e9. Date of Electronic Publication: 2019 Apr 04.
Publication Year :
2019

Abstract

Vascular endothelial growth factor (VEGF) is an important mediator of endothelial cell proliferation and angiogenesis via its receptor VEGFR2. A common tumor associated with elevated VEGFR2 signaling is infantile hemangioma that is caused by a rapid proliferation of vascular endothelial cells. The current first-line treatment for infantile hemangioma is the β-adrenoceptor antagonist, propranolol, although its mechanism of action is not understood. Here we have used bioluminescence resonance energy transfer and VEGFR2 genetically tagged with NanoLuc luciferase to demonstrate that oligomeric complexes involving VEGFR2 and the β <subscript>2</subscript> -adrenoceptor can be generated in both cell membranes and intracellular endosomes. These complexes are induced by agonist treatment and retain their ability to couple to intracellular signaling proteins. Furthermore, coupling of β <subscript>2</subscript> -adrenoceptor to β-arrestin2 is prolonged by VEGFR2 activation. These data suggest that protein-protein interactions between VEGFR2, the β <subscript>2</subscript> -adrenoceptor, and β-arrestin2 may provide insight into their roles in health and disease.<br /> (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
2451-9448
Volume :
26
Issue :
6
Database :
MEDLINE
Journal :
Cell chemical biology
Publication Type :
Academic Journal
Accession number :
30956148
Full Text :
https://doi.org/10.1016/j.chembiol.2019.02.014