The orphan receptor GPR139 signals via Gq/11 to oppose opioid effects

Journal of Biological Chemistry(2020)

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摘要
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 mu-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 G(q/11)and G(i/o)families. Using a panel of reporter assays in reconstituted HEK293T/17 cells, we found that GPR139 functions via the G(q/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 G(q/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.
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G protein-coupled receptor 139 (GPR139),brain,neuron,GPCR signaling,opioids,orphan receptor,medial habenula,G protein-coupled receptor (GPCR),heterotrimeric G protein,opiate opioid,cell signaling,cellular regulation,adenylate cyclase (adenylyl cyclase),GIRK channel
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