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Tau accumulation in a patient with pallidonigroluysian atrophy.

机译:Tau在pallidonigroluysian萎缩患者中蓄积。

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摘要

We studied the brain of a patient with pallidonigroluysian atrophy (PNLA) in whom argyrophilic and abnormally phosphorylated tau positive neurons and glia were identified in the brain on Gallyas-Braak silver staining and immunohistochemical analysis although neurofibrillary tangles were not seen by Bodian silver stain. Immunohistochemical studies using six anti-tau antibodies that recognize the different phosphorylated epitopes of tau protein revealed that these epitopes in neurons and glial cells share common characteristics with neurofibrillary tangles in Alzheimer's disease. Immunoblot analysis of phosphorylated tau protein showed major bands of 64 and 68 kDa and after dephosphorylation, tau consisted mainly of 4 repeat tau. No mutations were detected in the coding exons and their flanking intronic regions of the tau gene. This study suggests that PNLA is one of tauopathy and the biochemical characteristics of phosphorylated tau are similar to those found in progressive supranuclear palsy and corticobasal degeneration.
机译:我们研究了患有Pallidonigroluysian萎缩(PNLA)的患者的大脑,尽管通过Bodian银染未见神经原纤维缠结,但在Gallyas-Braak银染色和免疫组织化学分析中在大脑中鉴定出嗜银性和异常磷酸化的tau阳性神经元和神经胶质。使用六种抗tau抗体的免疫组织化学研究可识别tau蛋白的不同磷酸化表位,发现神经元和神经胶质细胞中的这些表位与阿尔茨海默氏病的神经原纤维缠结具有共同的特征。磷酸化tau蛋白的免疫印迹分析显示64和68 kDa的主要条带,去磷酸化后,tau主要由4个重复tau组成。在tau基因的编码外显子及其侧翼内含子区域未检测到突变。这项研究表明PNLA是tau病之一,磷酸化tau的生化特征与进行性核上性麻痹和皮质基底变性中发现的相似。

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