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Characteristic developmental expression of amyloid beta40, 42 and 43 in patients with Down syndrome.

机译:唐氏综合症患者中淀粉样蛋白β40、42和43的特征性发育表达。

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摘要

We immunohistochemically studied the expression of beta-amyloid precursor protein (APP), Abeta40, Abeta42, and Abeta43 in the frontal lobes of 20 Down syndrome (DS) patients and 13 controls. The immunoreactivity for each antibody was different in the degree of intensity and the chronological pattern of expression. APP and Abeta43 immunoreactivity was increased in neurons initially, and then Abeta43 and 42 immunoreactivity appeared in diffuse plaques from 32 years of age. APP and Abeta43 were characteristically observed in axons around senile plaques. Finally, Abeta40 immunoreactivity was detected in the cores of senile plaques. This time course of immunoreactive expression may be related to the pathogenetic process of Alzheimer-type dementia in DS, and the axonal damage in senile plaques may lead to the formation of neurofibrillary tangles (NFT) or neuronal death through axonal flow disturbance and accumulation of Abeta43 in cortical neurons.
机译:我们免疫组化研究了20名唐氏综合症(DS)患者和13名对照的额叶中β-淀粉样蛋白前体蛋白(APP),Abeta40,Abeta42和Abeta43的表达。每种抗体的免疫反应性在强度和表达的时间顺序上是不同的。最初,神经元中的APP和Abeta43免疫反应性增加,然后从32岁开始在弥漫性斑块中出现Abeta43和42免疫反应性。在老年斑周围的轴突中特征性地观察到APP和Abeta43。最后,在老年斑的核心中检测到Abeta40免疫反应性。免疫反应表达的这个时间过程可能与DS中Alzheimer型痴呆的致病过程有关,老年斑中轴突损伤可能导致神经原纤维缠结(NFT)的形成或由于轴突流动障碍和Abeta43积累而导致神经元死亡。在皮层神经元中

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