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Delineation of the GPR15 receptor‐mediated Gα protein signalling profile in recombinant mammalian cells.

Authors :
Deng, Yufang
Moo, Ee Von
Almería, Claudia Victoria Pérez
Gentry, Patrick R.
Vedel, Line
Mathiesen, Jesper M.
Bräuner‐Osborne, Hans
Source :
Basic & Clinical Pharmacology & Toxicology. Aug2022, Vol. 131 Issue 2, p104-113. 10p.
Publication Year :
2022

Abstract

The GPR15 receptor is a G protein‐coupled receptor (GPCR), which is activated by an endogenous peptide GPR15L(25–81) and a C‐terminal peptide fragment GPR15L(71–81). GPR15 signals through the Gi/o pathway to decrease intracellular cyclic adenosine 3′,5′‐monophosphate (cAMP). However, the activation profiles of the GPR15 receptor within Gi/o subtypes have not been examined. Moreover, whether the receptor can also couple to Gs, Gq/11 and G12/13 is unclear. Here, GPR15L(25–81) and GPR15L(71–81) are used as pharmacological tool compounds to delineate the GPR15 receptor‐mediated Gα protein signalling using a G protein activation assay and second messenger assay conducted on living cells. The results show that the GPR15 receptor preferentially couples to Gi/o rather than other pathways in both assays. Within the Gi/o family, the GPR15 receptor activates all the subtypes (Gi1, Gi2, Gi3, GoA, GoB and Gz). The Emax and activation rates of Gi1, Gi2, Gi3, GoA and GoB are similar, whilst the Emax of Gz is smaller and the activation rate is significantly slower. The potencies of both peptides toward each Gi/o subtype have been determined. Furthermore, the GPR15 receptor signals through Gi/o to inhibit cAMP accumulation, which could be blocked by the application of the Gi/o inhibitor pertussis toxin. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17427835
Volume :
131
Issue :
2
Database :
Academic Search Index
Journal :
Basic & Clinical Pharmacology & Toxicology
Publication Type :
Academic Journal
Accession number :
157908463
Full Text :
https://doi.org/10.1111/bcpt.13738