Back to Search Start Over

FZD 5 is a Gα q -coupled receptor that exhibits the functional hallmarks of prototypical GPCRs.

Authors :
Wright SC
Cañizal MCA
Benkel T
Simon K
Le Gouill C
Matricon P
Namkung Y
Lukasheva V
König GM
Laporte SA
Carlsson J
Kostenis E
Bouvier M
Schulte G
Hoffmann C
Source :
Science signaling [Sci Signal] 2018 Dec 04; Vol. 11 (559). Date of Electronic Publication: 2018 Dec 04.
Publication Year :
2018

Abstract

Frizzleds (FZDs) are a group of seven transmembrane-spanning (7TM) receptors that belong to class F of the G protein-coupled receptor (GPCR) superfamily. FZDs bind WNT proteins to stimulate diverse signaling cascades involved in embryonic development, stem cell regulation, and adult tissue homeostasis. Frizzled 5 (FZD <subscript>5</subscript> ) is one of the most studied class F GPCRs that promote the functional inactivation of the β-catenin destruction complex in response to WNTs. However, whether FZDs function as prototypical GPCRs has been heavily debated and, in particular, FZD <subscript>5</subscript> has not been shown to activate heterotrimeric G proteins. Here, we show that FZD <subscript>5</subscript> exhibited a conformational change after the addition of WNT-5A, which is reminiscent of class A and class B GPCR activation. In addition, we performed several live-cell imaging and spectrometric-based approaches, such as dual-color fluorescence recovery after photobleaching (dcFRAP) and resonance energy transfer (RET)-based assays that demonstrated that FZD <subscript>5</subscript> activated Gα <subscript>q</subscript> and its downstream effectors upon stimulation with WNT-5A. Together, these findings suggest that FZD <subscript>5</subscript> is a 7TM receptor with a bona fide GPCR activation profile and suggest novel targets for drug discovery in WNT-FZD signaling.<br /> (Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.)

Details

Language :
English
ISSN :
1937-9145
Volume :
11
Issue :
559
Database :
MEDLINE
Journal :
Science signaling
Publication Type :
Academic Journal
Accession number :
30514810
Full Text :
https://doi.org/10.1126/scisignal.aar5536