Neuroscience Research, Global Pharmaceutical Research and Development, Abbott, D-67061 Ludwigshafen, Germany.
J Neurosci. 2010 Aug 4;30(31):10369-79. doi: 10.1523/JNEUROSCI.5721-09.2010.
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.
β-淀粉样蛋白(Abeta)肽的低聚物已在阿尔茨海默病的早期神经病理学变化中得到证实。在这里,我们提出了一种具有与单体和纤维 Abeta 肽不同构象的合成 Abeta(20-42)低聚物(命名为 globulomer),能够产生高度 Abeta 低聚物特异性的单克隆抗体。源自 globulomer 的抗体特异性地检测各种 Abeta 制剂中的寡聚体,但不检测单体或纤维。Abeta 特异性抗体 A-887755 能够防止 Abeta 低聚物与原代海马神经元中的动力蛋白结合和切割,并逆转 globulomer 诱导的突触传递减少。在淀粉样前体蛋白(APP)转基因小鼠中,用 Abeta globulomer 进行疫苗接种并用 A-887755 进行治疗可改善新物体识别。认知改善可能归因于在用 A-887755 治疗后观察到的 APP 转基因小鼠海马突触棘密度缺陷的逆转。我们的研究结果表明,通过免疫疗法选择性减少 Abeta 低聚物足以使 APP 转基因小鼠的认知行为和突触缺陷正常化。