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The Orphan G Protein-Coupled Receptor 3 Modulates Amyloid-Beta Peptide Generation in Neurons
- Thathiah, Amantha, Spittaels, Kurt, Hoffmann, Marcel, Staes, Mik, Cohen, Adrian, Horré, Katrién, Vanbrabant, Mieke, Coun, Frea, Baekelandt, Veerle, Delacourte, André, Fischer, David F., Pollet, Dirk, De Strooper, Bart, Merchiers, Pascal
- Science 2009 v.323 no.5916 pp. 946-951
- Alzheimer disease, G-protein coupled receptors, animal models, brain, genomics, humans, neurons
- Deposition of the amyloid-β peptide is a pathological hallmark of Alzheimer's disease. A high-throughput functional genomics screen identified G protein-coupled receptor 3 (GPR3), a constitutively active orphan G protein-coupled receptor, as a modulator of amyloid-β production. Overexpression of GPR3 stimulated amyloid-β production, whereas genetic ablation of GPR3 prevented accumulation of the amyloid-β peptide in vitro and in an Alzheimer's disease mouse model. GPR3 expression led to increased formation and cell-surface localization of the mature γ-secretase complex in the absence of an effect on Notch processing. GPR3 is highly expressed in areas of the normal human brain implicated in Alzheimer's disease and is elevated in the sporadic Alzheimer's disease brain. Thus, GPR3 represents a potential therapeutic target for the treatment of Alzheimer's disease.