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肌萎缩侧索硬化症合并痴呆、关岛肌萎缩侧索硬化症及关岛帕金森病痴呆综合征中海马颗粒细胞泛素免疫反应性的比较研究

Comparative study of ubiquitin immunoreactivity of hippocampal granular cells in amyotrophic lateral sclerosis with dementia, Guamanian amyotrophic lateral sclerosis and Guamanian parkinsonism-dementia complex.

作者信息

Ikemoto A, Hirano A, Akiguchi I, Kimura J

机构信息

Department of Pathology, Montefiore Medical Center, Bronx, New York, NY 10467, USA.

出版信息

Acta Neuropathol. 1997 Mar;93(3):265-70. doi: 10.1007/s004010050613.

Abstract

This report concerns an investigation on ubiquitin immunoreactivity in the neuronal perikarya of hippocampal granular cells in Guamanian amyotrophic lateral sclerosis (G-ALS) and Guamanian parkinsonism-dementia complex (G-PDC). Specimens from two non-Guamanian cases of ALS with dementia (ALS-D) were included for comparison. Histologically normal hippocampi from five adults served as controls. Antibodies to ubiquitin and tau protein were used throughout. Most Guamanian patients examined had granular cells with perikaryal ubiquitin immunoreactivity in the dentate gyrus, but in comparison to ALS-D, the frequency of ubiquitin-positive neurons was significantly lower. Tau-positive granular cells were detected in most Guamanian patients, but not in ALS-D. There was a relationship between the numbers of ubiquitin-positive and tau-positive neurons in the dentate granular cell layer of G-ALS and G-PDC patients. This was verified on sections double immunostained for tau protein and ubiquitin. The present findings suggest that the ubiquitin-positive materials observed in the perikarya of the dentate granular cells of patients with G-ALS or with G-PDC seem to be Alzheimer's neurofibrillary tangles rather than the typical ubiquitin-positive intracytoplasmic neuronal inclusions, characteristics of ALS-D. Our data would indicate that different mechanisms are involved in the geneses of cortical neuronal degeneration and decline in cognitive function in ALS-D, G-ALS and G-PDC.

摘要

本报告涉及对关岛肌萎缩侧索硬化症(G-ALS)和关岛帕金森病痴呆综合征(G-PDC)患者海马颗粒细胞神经元胞体中泛素免疫反应性的研究。纳入了两例非关岛型伴痴呆的肌萎缩侧索硬化症(ALS-D)病例的标本进行比较。选取了五名成年人组织学正常的海马作为对照。全程使用泛素和tau蛋白抗体。大多数接受检查的关岛患者齿状回中的颗粒细胞胞体存在泛素免疫反应性,但与ALS-D相比,泛素阳性神经元的频率显著更低。大多数关岛患者检测到tau阳性颗粒细胞,但ALS-D患者未检测到。G-ALS和G-PDC患者齿状颗粒细胞层中泛素阳性和tau阳性神经元的数量之间存在关联。这在tau蛋白和泛素双重免疫染色的切片上得到了证实。目前的研究结果表明,在G-ALS或G-PDC患者齿状颗粒细胞胞体中观察到的泛素阳性物质似乎是阿尔茨海默神经原纤维缠结,而非ALS-D特征性的典型泛素阳性胞质内神经元包涵体。我们的数据表明,ALS-D、G-ALS和G-PDC患者皮质神经元变性和认知功能下降的发生涉及不同机制。

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