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阿尔茨海默病、帕金森病和唐氏综合征患者嗅黏膜中的β-淀粉样肽和淀粉样前体蛋白。

Beta-Amyloid peptide and amyloid precursor proteins in olfactory mucosa of patients with Alzheimer's disease, Parkinson's disease, and Down syndrome.

作者信息

Crino P B, Martin J A, Hill W D, Greenberg B, Lee V M, Trojanowski J Q

机构信息

Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, USA.

出版信息

Ann Otol Rhinol Laryngol. 1995 Aug;104(8):655-61. doi: 10.1177/000348949510400812.

DOI:10.1177/000348949510400812
PMID:7639477
Abstract

Dystrophic neurites are present in olfactory epithelium (OE) of patients with Alzheimer's disease (AD), Parkinson's disease (PD), and Down syndrome (DS) and occasionally in normal individuals. Cultured olfactory neuroblasts from AD patients generate carboxy terminal amyloid precursor protein (APP) fragments that contain beta-amyloid (A beta), but it is not known if deposits of A beta and/or APP fragments occur in the OE of individuals with or without AD, PD, or DS. To determine if A beta accumulates in the OE in situ, we probed postmortem samples of olfactory mucosa from patients with AD, PD, and AD (PD/AD), and DS and AD (DS/AD), as well as from controls, using polyclonal and monoclonal antibodies to A beta and flanking sequences in APPs. Samples of OE also were examined by thioflavin-S and electron microscopy. Labeling of A beta was observed in 10 of 12 AD cases, 2 of 3 PD/AD cases, 3 of 4 DS/AD cases, 3 of 10 adult controls, and 4 of 6 fetal cases. The A beta staining was seen in the basal third of the OE, in axons projecting through the lamina propria, and in metaplastic respiratory epithelium within the OE. Antibodies to other APP domains stained the OE of patients and controls. Thioflavin-S staining was present in the basal third of the OE of 8 of 9 AD patients and several PD/AD and DS/AD patients, but only in rare cells of 3 controls. Electron microscopy did not reveal amyloid fibrils in the OE.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

营养不良性神经突存在于阿尔茨海默病(AD)、帕金森病(PD)和唐氏综合征(DS)患者的嗅上皮(OE)中,偶尔也见于正常个体。来自AD患者的培养嗅成神经细胞会产生含有β-淀粉样蛋白(Aβ)的羧基末端淀粉样前体蛋白(APP)片段,但尚不清楚Aβ和/或APP片段的沉积物是否存在于患有或未患有AD、PD或DS的个体的OE中。为了确定Aβ是否在原位OE中积累,我们使用针对Aβ和APP侧翼序列的多克隆和单克隆抗体,对AD、PD和AD(PD/AD)、DS和AD(DS/AD)患者以及对照的嗅黏膜死后样本进行了检测。OE样本也通过硫黄素-S和电子显微镜进行了检查。在12例AD病例中的10例、3例PD/AD病例中的2例、4例DS/AD病例中的3例、10例成人对照中的3例以及6例胎儿病例中的4例中观察到了Aβ标记。Aβ染色见于OE的基底三分之一、穿过固有层的轴突以及OE内的化生呼吸上皮。针对APP其他结构域的抗体对患者和对照的OE进行了染色。9例AD患者中的8例以及数例PD/AD和DS/AD患者的OE基底三分之一处存在硫黄素-S染色,但仅在3例对照的罕见细胞中出现。电子显微镜未在OE中发现淀粉样纤维。(摘要截断于250字)

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