| Literature DB >> 32576659 |
Hannah M Stoveken1, Stefano Zucca1, Ikuo Masuho1, Brock Grill1, Kirill A Martemyanov2.
Abstract
The interplay between G protein-coupled receptors (GPCRs) is critical for controlling neuronal activity that shapes neuromodulatory outcomes. Recent evidence indicates that the orphan receptor GPR139 influences opioid modulation of key brain circuits by opposing the actions of the µ-opioid receptor (MOR). However, the function of GPR139 and its signaling mechanisms are poorly understood. In this study, we report that GPR139 activates multiple heterotrimeric G proteins, including members of the Gq/11 and Gi/o families. Using a panel of reporter assays in reconstituted HEK293T/17 cells, we found that GPR139 functions via the Gq/11 pathway and thereby distinctly regulates cellular effector systems, including stimulation of cAMP production and inhibition of G protein inward rectifying potassium (GIRK) channels. Electrophysiological recordings from medial habenular neurons revealed that GPR139 signaling via Gq/11 is necessary and sufficient for counteracting MOR-mediated inhibition of neuronal firing. These results uncover a mechanistic interplay between GPCRs involved in controlling opioidergic neuromodulation in the brain.Entities:
Keywords: G protein-coupled receptor (GPCR); G protein-coupled receptor 139 (GPR139); GIRK channel; GPCR signaling; adenylate cyclase (adenylyl cyclase); brain; cell signaling; cellular regulation; heterotrimeric G protein; medial habenula; neuron; opiate opioid; opioids; orphan receptor
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Year: 2020 PMID: 32576659 PMCID: PMC7397111 DOI: 10.1074/jbc.AC120.014770
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157