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阿尔茨海默病中分子量为60000的蛋白质磷酸化增加与新皮质神经原纤维缠结相关。

Increased Mr 60,000 protein phosphorylation is correlated with neocortical neurofibrillary tangles in Alzheimer's disease.

作者信息

Saitoh T, Hansen L A, Dobkins K R, Terry R D

机构信息

Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla 92093.

出版信息

J Neuropathol Exp Neurol. 1988 Jan;47(1):1-8. doi: 10.1097/00005072-198801000-00001.

Abstract

Increased Mr 60,000 protein phosphorylation has been found in the cytosol fraction of brain tissue from Alzheimer's disease patients. A correlation between this biochemical change and the morphologic abnormalities found in Alzheimer's disease was sought. Three neuropathologic features were studied: neurofibrillary tangles and neuritic plaques, findings characteristic of Alzheimer's disease, and gliosis, a non-specific change. The number of tangles correlated well with the extent of Mr 60,000 protein phosphorylation (p less than 0.001); but the number of plaques did not. To investigate the possibility that gliosis causes the increased Mr 60,000 protein phosphorylation, cases of Pick's disease and multi-infarct dementia were also studied. The levels of Mr 60,000 protein phosphorylation in these cases were comparable to those seen in normal controls. These findings suggest that the increased Mr 60,000 protein phosphorylation is closely related to diseased, tangle-bearing neurons and is not directly related to neuritic plaque formation or secondary gliosis.

摘要

在阿尔茨海默病患者脑组织的胞质溶胶部分发现分子量为60,000的蛋白质磷酸化增加。人们探寻了这种生化变化与阿尔茨海默病中发现的形态学异常之间的相关性。研究了三种神经病理学特征:神经原纤维缠结和神经炎性斑块,这是阿尔茨海默病的特征性表现,以及胶质增生,一种非特异性变化。缠结的数量与分子量为60,000的蛋白质磷酸化程度密切相关(p小于0.001);但斑块的数量并非如此。为了研究胶质增生导致分子量为60,000的蛋白质磷酸化增加的可能性,还对匹克病和多发性梗死性痴呆病例进行了研究。这些病例中分子量为60,000的蛋白质磷酸化水平与正常对照相当。这些发现表明,分子量为60,000的蛋白质磷酸化增加与患病的、带有缠结的神经元密切相关,与神经炎性斑块形成或继发性胶质增生无直接关系。

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