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帕金森病和路易体痴呆中路易小体丝状成分上NACP/α-突触核蛋白表位的免疫电子显微镜证实

Immunoelectron-microscopic demonstration of NACP/alpha-synuclein-epitopes on the filamentous component of Lewy bodies in Parkinson's disease and in dementia with Lewy bodies.

作者信息

Arima K, Uéda K, Sunohara N, Hirai S, Izumiyama Y, Tonozuka-Uehara H, Kawai M

机构信息

Department of Ultrastructure and Histochemistry, Tokyo Institute of Psychiatry, 2-1-8 Kamikitazawa, Setagaya-ku, Tokyo 156-8585, Japan.

出版信息

Brain Res. 1998 Oct 12;808(1):93-100. doi: 10.1016/s0006-8993(98)00734-3.

DOI:10.1016/s0006-8993(98)00734-3
PMID:9795161
Abstract

We examined brains from Parkinson's disease and from dementia with Lewy bodies (LBs) by using antibodies to NACP/alpha-synuclein. Immunohistochemically, all of the antibodies against the amino-terminal region, NAC domain, and carboxyl-terminal region of NACP labeled not only LBs, pale bodies (PBs), and dystrophic neurites, but also fine thread-like structures in the neuronal perikarya (perikaryal threads) in the hypothalamus and brainstem nuclei. On electron microscopy, immunoreactive products were found to label the 9 to 12 nm-thick filamentous component (LB-filaments) of LBs, PBs, and perikaryal threads. The NACP-immunoreactive perikaryal threads, consisting of small bundles of LB-filaments and randomly oriented LB-filaments, presumably represent an initial stage of LB- or PB-formation. The present study indicates that the entire molecule of NACP is involved in the neuronal filament-aggregating processes of LB disorders.

摘要

我们使用针对NACP/α-突触核蛋白的抗体,对帕金森病和路易体痴呆(LBs)患者的大脑进行了检查。免疫组织化学研究显示,所有针对NACP氨基末端区域、NAC结构域和羧基末端区域的抗体,不仅标记了路易小体(LBs)、苍白小体(PBs)和营养不良性神经突,还标记了下丘脑和脑干核中神经元胞体(胞体细丝)内的细丝状结构。电子显微镜检查发现,免疫反应产物标记了LBs、PBs和胞体细丝中9至12纳米厚的丝状成分(LB细丝)。由小束LB细丝和随机排列的LB细丝组成的NACP免疫反应性胞体细丝,可能代表了LB或PB形成的初始阶段。本研究表明,NACP的整个分子参与了LB疾病的神经元细丝聚集过程。

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