Journal of Neuroscience · 2010 · 112 citations · 34 references
Life SciencesNeurobiologyNeuroscienceMolecular NeuroscienceMonoclonal AntibodiesNeurodegenerationAlzheimer DiseaseNeurodegenerative DiseasesNeurodegenerative DisordersProtein AggregationTherapeutic Antibody DevelopmentTherapeutic Monoclonal AntibodiesAmyloid Beta AggregationAmyloid Beta PeptidesAmyloid StructureAntibodiesSynaptic DensitySynaptic Spine LossTherapeutic Vaccine EfficacyTransgenic Mice
Oligomers of the beta-amyloid (Abeta) peptide have been indicated in early neuropathologic changes in Alzheimer's disease. Here, we present a synthetic Abeta(20-42) oligomer (named globulomer) with a different conformation to monomeric and fibrillar Abeta peptide, enabling the generation of highly Abeta oligomer-specific monoclonal antibodies. The globulomer-derived antibodies specifically detect oligomeric but not monomeric or fibrillar Abeta in various Abeta preparations. The globulomer-specific antibody A-887755 was able to prevent Abeta oligomer binding and dynamin cleavage in primary hippocampal neurons and to reverse globulomer-induced reduced synaptic transmission. In amyloid precursor protein (APP) transgenic mice, vaccination with Abeta globulomer and treatment with A-887755 improved novel object recognition. The cognitive improvement is likely attributable to reversing a deficit in hippocampal synaptic spine density in APP transgenic mice as observed after treatment with A-887755. Our findings demonstrate that selective reduction of Abeta oligomers by immunotherapy is sufficient to normalize cognitive behavior and synaptic deficits in APP transgenic mice.
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