dc.contributor.author |
Finlay, David |
en |
dc.contributor.author |
Cawston, Erin |
en |
dc.contributor.author |
Grimsey, Natasha |
en |
dc.contributor.author |
Hunter, MR |
en |
dc.contributor.author |
Korde, A |
en |
dc.contributor.author |
Vemuri, VK |
en |
dc.contributor.author |
Makriyannis, A |
en |
dc.contributor.author |
Glass, Michelle |
en |
dc.date.accessioned |
2017-08-23T22:26:35Z |
en |
dc.date.issued |
2017-08 |
en |
dc.identifier.citation |
British Journal of Pharmacology 174(15):2545-2562 Aug 2017 |
en |
dc.identifier.issn |
0007-1188 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/35307 |
en |
dc.description.abstract |
CB1 receptor signalling is canonically mediated through inhibitory Gαi proteins, but occurs through other G proteins under some circumstances, Gαs being the most characterized secondary pathway. Determinants of this signalling switch identified to date include Gαi blockade, CB1 /D2 receptor co-stimulation, CB1 agonist class and cell background. Hence, we examined the effects of receptor number and different ligands on CB1 receptor signalling.CB1 receptors were expressed in HEK cells at different levels, and signalling characterized for cAMP by real-time BRET biosensor -CAMYEL - and for phospho-ERK by AlphaScreen. Homogenate and whole cell radioligand binding assays were performed to characterize AM6544, a novel irreversible CB1 receptor antagonist.In HEK cells expressing high levels of CB1 receptors, agonist treatment stimulated cAMP, a response not known to be mediated by receptor number. Δ9 -THC and BAY59-3074 increased cAMP only in high-expressing cells pretreated with pertussis toxin, and agonists demonstrated more diverse signalling profiles in the stimulatory pathway than the canonical inhibitory pathway. Pharmacological CB1 receptor knockdown and Gαi 1 supplementation restored canonical Gαi signalling to high-expressing cells. Constitutive signalling in both low- and high-expressing cells was Gαi -mediated.CB1 receptor coupling to opposing G proteins is determined by both receptor and G protein expression levels, which underpins a mechanism for non-canonical signalling in a fashion consistent with Gαs signalling. CB1 receptors mediate opposite consequences in endpoints such as tumour viability depending on expression levels; our results may help to explain such effects at the level of G protein coupling. |
en |
dc.format.medium |
Print-Electronic |
en |
dc.language |
eng |
en |
dc.publisher |
Wiley-Blackwell |
en |
dc.relation.ispartofseries |
British Journal of Pharmacology |
en |
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.title |
Gαs signalling of the CB1 receptor and the influence of receptor number |
en |
dc.type |
Journal Article |
en |
dc.identifier.doi |
10.1111/bph.13866 |
en |
pubs.issue |
15 |
en |
pubs.begin-page |
2545 |
en |
pubs.volume |
174 |
en |
dc.rights.holder |
Copyright: Wiley-Blackwell |
en |
dc.identifier.pmid |
28516479 |
en |
pubs.end-page |
2562 |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RestrictedAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
626907 |
en |
pubs.org-id |
Medical and Health Sciences |
en |
pubs.org-id |
Medical Sciences |
en |
pubs.org-id |
Pharmacology |
en |
dc.identifier.eissn |
1476-5381 |
en |
pubs.record-created-at-source-date |
2017-08-24 |
en |
pubs.dimensions-id |
28516479 |
en |