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大量修饰tau蛋白的积累和正常tau蛋白的严重耗竭是阿尔茨海默病大脑皮质和白质的特征。采用水合高压灭菌法进行验证。

Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method.

作者信息

Shin R W, Iwaki T, Kitamoto T, Sato Y, Tateishi J

机构信息

Department of Neuropathology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Am J Pathol. 1992 Apr;140(4):937-45.

PMID:1373272
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1886360/
Abstract

Using the hydrated autoclaving method, a new immunohistochemical procedure to enhance tau immunoreactivity in formalin-fixed brain tissue, the authors recently reported that tau protein is detected in neuronal cell bodies and proximal dendrites, gray matter neuropil, axons, and glial cells in normal human hippocampus and neocortex. In the this study, the authors performed a comparative study of the distribution of normal and modified forms of tau in Alzheimer's disease (AD) and control brains. In the cerebral cortex and white matter of AD brains, a massive accumulation of modified tau and/or severe depletion of normal tau were documented in all the tau compartments. In mild AD cases, gray matter neuropil, axons, and glial cells were less severely involved than neuronal perikarya. In the controls, neuronal perikarya were often involved by modified tau accumulation, but the other compartments showed normal distribution. These observations suggest that modifications of tau which lead to neurofibrillary lesions in AD may begin in neuronal perikarya and extend to the other tau compartments in advanced stages of the disease.

摘要

作者最近报告称,使用水合高压灭菌法(一种增强福尔马林固定脑组织中tau免疫反应性的新免疫组织化学方法),在正常人海马体和新皮质的神经元细胞体、近端树突、灰质神经纤维网、轴突和神经胶质细胞中检测到了tau蛋白。在本研究中,作者对阿尔茨海默病(AD)和对照大脑中正常和修饰形式的tau分布进行了比较研究。在AD大脑的大脑皮质和白质中,所有tau区室均记录到修饰tau的大量积累和/或正常tau的严重耗竭。在轻度AD病例中,灰质神经纤维网、轴突和神经胶质细胞受累程度低于神经元胞体。在对照组中,神经元胞体常因修饰tau的积累而受累,但其他区室显示正常分布。这些观察结果表明,导致AD神经原纤维病变的tau修饰可能始于神经元胞体,并在疾病晚期扩展到其他tau区室。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/f1ae18ecfb12/amjpathol00088-0185-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/5cda7f64f8fe/amjpathol00088-0181-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/584cad6337ce/amjpathol00088-0182-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/55be5d064616/amjpathol00088-0182-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/1f7df07bc06b/amjpathol00088-0183-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/73bc113d1701/amjpathol00088-0184-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/f1ae18ecfb12/amjpathol00088-0185-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/5cda7f64f8fe/amjpathol00088-0181-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/584cad6337ce/amjpathol00088-0182-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/55be5d064616/amjpathol00088-0182-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/1f7df07bc06b/amjpathol00088-0183-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/73bc113d1701/amjpathol00088-0184-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d41/1886360/f1ae18ecfb12/amjpathol00088-0185-a.jpg

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