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Identification and characterization of select oxysterols as ligands for GPR17
Author(s) -
Harrington Anthony W.,
Liu Changlu,
Phillips Naomi,
Nepomuceno Diane,
Kuei Chester,
Chang Joseph,
Chen Weixuan,
Sutton Steven W.,
O'Malley Daniel,
Pham Ly,
Yao Xiang,
Sun Siquan,
Bonaventure Pascal
Publication year - 2023
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.15969
Subject(s) - orphan receptor , activator (genetics) , receptor , biochemistry , biology , microbiology and biotechnology , chemistry , transcription factor , gene
Background and Purpose G‐protein coupled receptor 17 (GPR17) is an orphan receptor involved in the process of myelination, due to its ability to inhibit the maturation of oligodendrocyte progenitor cells (OPCs) into myelinating oligodendrocytes. Despite multiple claims that the biological ligand has been identified, it remains an orphan receptor. Experimental Approach Seventy‐seven oxysterols were screened in a cell‐free [ 35 S]GTPγS binding assay using membranes from cells expressing GPR17. The positive hits were characterized using adenosine 3′,5′ cyclic monophosphate (cAMP), inositol monophosphate (IP1) and calcium mobilization assays, with results confirmed in rat primary oligodendrocytes. Rat and pig brain extracts were separated by high‐performance liquid chromatography (HPLC) and endogenous activator(s) were identified in receptor activation assays. Gene expression studies of GPR17 , and CYP46A1 (cytochrome P450 family 46 subfamily A member 1) enzymes responsible for the conversion of cholesterol into specific oxysterols, were performed using quantitative real‐time PCR. Key Results Five oxysterols were able to stimulate GPR17 activity, including the brain cholesterol, 24(S)‐hydroxycholesterol (24S‐HC). A specific brain fraction from rat and pig extracts containing 24S‐HC activates GPR17 in vitro. Expression of Gpr17 during mouse brain development correlates with the expression of Cyp46a1 and the levels of 24S‐HC itself. Other active oxysterols have low brain concentrations below effective ranges. Conclusions and Implications Oxysterols, including but not limited to 24S‐HC, could be physiological activators for GPR17 and thus potentially regulate OPC differentiation and myelination through activation of the receptor.