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ReportsThe Orphan G Protein–Coupled Receptor 3 Modulates Amyloid-Beta Peptide Generation in 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
1 Department of Molecular and Developmental Genetics, Vlaams Institute for Biotechnology. -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.
2 Center for Human Genetics, Catholic University of Leuven, Herestraat 49, 3000 Leuven, Belgium. 3 Galapagos, Generaal De Wittelaan L11 A3, 2800 Mechelen, Belgium. 4 Laboratory for Neurobiology and Gene Therapy, Division of Molecular Medicine, Catholic University of Leuven, Kapucijnenvoer 33, 3000 Leuven. 5 BioFocus DPI, a Galapagos company, Darwinweg 24, 2333 CR Leiden, Netherlands. 6 INSERM Unit 837, Jean-Pierre Aubert Research Center, 1 Place de Verdun, 59045 Lille Cedex, France. * Present address: Tibotec BVBA, Generaal De Wittelaan L11B3, 2800 Mechelen, Belgium.
¶ Present address: Ablynx NV, Technologie Park 4, 9052 Zwijnaarde, Belgium. || To whom correspondence should be addressed. E-mail: david.fischer{at}glpg.com (D.F.F.); bart.destrooper{at}med.kuleuven.be (B.D.S.)
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Science. ISSN 0036-8075 (print), 1095-9203 (online)