Trans-synaptic interaction of orphan GPCR GPR88 and adhesion GPCR BAI3 through C1ql1 maintains synapse integrity

GPR88 is an orphan GPCR with genetic variants associated with multiple neuropsychiatric conditions. GPR88 exhibits enriched expression in the striatum, olfactory tubercle, and inferior olive. Despite these functional associations, its endogenous ligand and its downstream molecular pathways remain unresolved. Here, we found that climbing fiber (CF)-localized GPR88 regulates CF-Purkinje cell synapses in the cerebellum and associative learning behaviors. The results support the CF-secreted protein C1ql1 as the ligand of GPR88 and further revealed that C1ql1 activates biased Gq signaling to enhance CF synapses. Last, we demonstrated that GPR88 anchors C1ql1 and, via C1ql1, forms a tripartite complex with the postsynaptic adhesion GPCR BAI3 in vitro. These findings resolve the orphan status of GPR88 and likely reveal a mechanism by which a secreted protein links two GPCRs to fine-tune synaptic signaling at pre- and postsynaptic sites.

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Publication Details

Journal
Science Advances
Published
2026-10-28
DOI
https://doi.org/10.1126/sciadv.aec0867
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Trans-synaptic interaction of orphan GPCR GPR88 and adhesion GPCR BAI3 through C1ql1 maintains synapse integrity

Zhiyi Wei, Jie Cheng, Ke-Ke Xing, Chao Zhang et al.
Science Advances
Neuroscience and Neuropharmacology Research
article

Trans-synaptic interaction of orphan GPCR GPR88 and adhesion GPCR BAI3 through C1ql1 maintains synapse integrity

Zhiyi Wei, Jie Cheng, Ke-Ke Xing, Chao Zhang, Xiao Yu, Qingbiao Meng, Lulu Guo, Bo Zhang, Tao Chen, Xuan Li, Jin‐Peng Sun, Liming Qin, Ying Han, Qin Huang, Liangyu Liao
article en

Abstract

GPR88 is an orphan GPCR with genetic variants associated with multiple neuropsychiatric conditions. GPR88 exhibits enriched expression in the striatum, olfactory tubercle, and inferior olive. Despite these functional associations, its endogenous ligand and its downstream molecular pathways remain unresolved. Here, we found that climbing fiber (CF)-localized GPR88 regulates CF-Purkinje cell synapses in the cerebellum and associative learning behaviors. The results support the CF-secreted protein C1ql1 as the ligand of GPR88 and further revealed that C1ql1 activates biased Gq signaling to enhance CF synapses. Last, we demonstrated that GPR88 anchors C1ql1 and, via C1ql1, forms a tripartite complex with the postsynaptic adhesion GPCR BAI3 in vitro. These findings resolve the orphan status of GPR88 and likely reveal a mechanism by which a secreted protein links two GPCRs to fine-tune synaptic signaling at pre- and postsynaptic sites.

Science AdvancesVol. 12(44)
Shandong University (CN), Peking University (CN), Southern University of Science and Technology (CN), Shenzhen Bay Laboratory (CN), Qilu Hospital of Shandong University (CN), Shandong First Medical University (CN), Shenzhen Medical Academy of Research and Translation (CN), Air Force Medical University (CN)
National Natural Science Foundation of China, Fourth Military Medical University, Southern University of Science and Technology, Shenzhen-Hong Kong Institute of Brain Science, Shenzhen Bay Laboratory, National Institutes of Health, University of California, San Francisco
Openalex Percentile: Top 20%
Neuroscience and Neuropharmacology Research
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