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无Pick小体的非典型Pick病的泛素免疫组织化学研究

Ubiquitin-immunohistochemical investigation of atypical Pick's disease without Pick bodies.

作者信息

Iseki E, Li F, Odawara T, Hino H, Suzuki K, Kosaka K, Akiyama H, Ikeda K, Kato M

机构信息

Department of Psychiatry, Yokohama City University School of Medicine, Yokohama, Japan.

出版信息

J Neurol Sci. 1998 Aug 14;159(2):194-201. doi: 10.1016/s0022-510x(98)00168-3.

DOI:10.1016/s0022-510x(98)00168-3
PMID:9741407
Abstract

Six cases of atypical Pick's disease (PD) without Pick bodies (PB) were examined immunohistochemically. These cases showed severe neuronal loss with gliosis predominantly in the temporal cortices. Ubiquitin immunohistochemistry revealed ubiquitin-positive intraneuronal inclusions in the dentate gyrus and ubiquitin-positive neurites in the cerebral cortex. In the dentate gyrus, the dendrites in the stratum moleculare as well as the intraneuronal inclusions in the granular cells were positively stained. Both structures were composed of ubiquitin-positive ribosome-like granular components and a few filamentous components immunoelectron-microscopically. In the cerebral cortex, ubiquitin-positive neurites were distributed in layers II-IIIab and layers V-VI, and were considered to be the distal dendrites from the small neurons. The dendrites and perikarya of these neurons contained ubiquitin-positive components similar to those in the dentate gyrus. Some ubiquitin-positive neurites were also found in the hippocampal subiculum, amygdala and striatum. The results of this study suggest that the granular cells in the dentate gyrus and the small neurons in the cerebral cortex share common ubiquitin-related and ribosome-associated abnormalities in both the perikarya and dendrites, that the degeneration of the perforant pathway caused by the parahippocampal lesion participates in the ubiquitin related abnormalities in the granular cells, and that PD cases with and without PB have common affected neurons, as shown immunohistochemically.

摘要

对6例无Pick小体(PB)的非典型Pick病(PD)进行了免疫组织化学检查。这些病例主要在颞叶皮质显示严重的神经元丢失伴胶质增生。泛素免疫组织化学显示齿状回中有泛素阳性的神经元内包涵体,大脑皮质中有泛素阳性的神经突。在齿状回中,分子层中的树突以及颗粒细胞中的神经元内包涵体均呈阳性染色。免疫电镜观察发现,这两种结构均由泛素阳性的核糖体样颗粒成分和一些丝状成分组成。在大脑皮质中,泛素阳性神经突分布于II - IIIab层和V - VI层,被认为是小神经元的远端树突。这些神经元的树突和胞体含有与齿状回中相似的泛素阳性成分。在海马下托、杏仁核和纹状体中也发现了一些泛素阳性神经突。本研究结果表明,齿状回中的颗粒细胞和大脑皮质中的小神经元在胞体和树突中具有共同的与泛素相关和核糖体相关的异常,海马旁病变导致的穿通通路退变参与了颗粒细胞中与泛素相关的异常,并且免疫组织化学显示有PB和无PB的PD病例具有共同的受累神经元。

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