PT  - JOURNAL ARTICLE
AU  - Seshat M. Mack
AU  - Ivone Gomes
AU  - Amanda K. Fakira
AU  - Mariana  Lemos Duarte
AU  - Achla Gupta
AU  - Lloyd Fricker
AU  - Lakshmi A. Devi
TI  - GPR83 Engages Endogenous Peptides from Two Distinct Precursors to Elicit Differential Signaling
AID  - 10.1124/molpharm.122.000487
DP  - 2022 Jul 01
TA  - Molecular Pharmacology
PG  - 29--38
VI  - 102
IP  - 1
4099  - http://molpharm.aspetjournals.org/content/102/1/29.short
4100  - http://molpharm.aspetjournals.org/content/102/1/29.full
SO  - Mol Pharmacol2022 Jul 01; 102
AB  - PEN is an abundant neuropeptide that activates G protein-coupled receptor 83 (GPR83), which is considered a novel therapeutic target due to its roles in regulation of feeding-, reward-, and anxiety-related behaviors. The major form of PEN in the brain is 22 residues in length. Previous studies have identified shorter forms of PEN in mouse brain and neuroendocrine cells; these shorter forms were named PEN18, PEN19, and PEN20, with the number reflecting the length of the peptide. The C-terminal five residues of PEN20 are identical to the C-terminus of a procholecystokinin (proCCK)-derived peptide, named proCCK56-62, that is present in mouse brain. ProCCK56-62 is highly conserved across species, although it has no homology to the bioactive cholecystokinin domain. ProCCK56-62 and a longer form, proCCK56-63, were tested for their ability to engage GPR83. Both peptides bind GPR83 with high affinity, activate second messenger pathways, and induce ligand-mediated receptor endocytosis. Interestingly, the shorter PEN peptides, ProCC56-62 and ProCCK56-63, differentially activate signal transduction pathways. Whereas PEN22 and PEN20 facilitate receptor coupling to Gαi, PEN18, PEN19, and ProCCK peptides facilitate coupling to Gαs. Furthermore, the ProCCK peptides exhibit dose-dependent Gα subtype selectivity in that they facilitate coupling to Gαs at low concentrations and Gαi at high concentrations. These data demonstrate that peptides derived from two distinct peptide precursors can differentially activate GPR83 and that GPR83 exhibits Gα subtype preference depending on the nature and concentration of the peptide. These results are consistent with the emerging idea that endogenous neuropeptides function as biased ligands.SIGNIFICANCE STATEMENT We found that peptides derived from procholecystokinin (proCCK) bind and activate G protein-coupled receptor 83, which is known to bind peptides derived from proSAAS. Different forms of the proCCK- and proSAAS-derived peptides show biased agonism, activating Gαs or Gαi depending on the length of the peptide and/or its concentration.