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首页> 外文期刊>Brain pathology >Intraneuronal APP/A beta trafficking and plaque formation in beta-amyloid precursor protein and presenilin-1 transgenic mice.
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Intraneuronal APP/A beta trafficking and plaque formation in beta-amyloid precursor protein and presenilin-1 transgenic mice.

机译:在β淀粉样蛋白前体蛋白和presenilin-1转基因小鼠中神经内APP / Aβ转运和斑块形成。

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摘要

Neuropil deposition of beta-amyloid peptides A beta40 and A beta42 is believed to be the key event in the neurodegenerative processes of Alzheimer's disease (AD). Since A beta seems to carry a transport signal that is required for axonal sorting of its precursor beta-amyloid precursor protein (APP), we studied the intraneuronal staining profile of A beta peptides in a transgenic mouse model expressing human mutant APP751 (KM670/671NL and V7171) and human mutant presenilin-1 (PS-1 M146L) in neurons. Using surface plasmon resonance we analyzed the A beta antibodies and defined their binding profile to APP, A beta40 and A beta42. Immunohistochemical staining revealed that intraneuronal A beta40 and A beta42 staining preceded plaque deposition, which started at 3 months of age. A beta was observed in the somatodendritic and axonal compartments of many neurons. Interestingly, the striatum, which lacks transgenic APP expression harbored many plaques at 10 months of age. This is most likely due to an APP/A beta transport problem and may be a model region to study APP/A beta trafficking as an early pathological event.
机译:β-淀粉样蛋白肽A beta40和A beta42的神经纤维沉积被认为是阿尔茨海默氏病(AD)神经退行性过程中的关键事件。由于A beta似乎携带了对其前体β-淀粉样蛋白前体蛋白(APP)进行轴突分选所需的运输信号,因此我们在表达人类突变体APP751(KM670 / 671NL)的转基因小鼠模型中研究了A beta肽的神经内染色特性和V7171)和神经元中的人类突变体早老素-1(PS-1 M146L)。使用表面等离子体共振,我们分析了A beta抗体,并定义了它们与APP,A beta40和A beta42的结合情况。免疫组织化学染色显示,神经内A beta40和A beta42染色先于3个月大的斑块沉积。在许多神经元的躯体树突状和轴突区室中观察到β。有趣的是,缺乏转基因APP表达的纹状体在10个月大时有许多斑块。这很可能是由于APP / A Beta的运输问题造成的,并且可能是研究APP / A Beta交易作为早期病理事件的模型区域。

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