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阿尔茨海默病的神经原纤维缠结与轴突微管相关蛋白tau(tau蛋白)具有共同的抗原决定簇。

Neurofibrillary tangles of Alzheimer disease share antigenic determinants with the axonal microtubule-associated protein tau (tau).

作者信息

Wood J G, Mirra S S, Pollock N J, Binder L I

出版信息

Proc Natl Acad Sci U S A. 1986 Jun;83(11):4040-3. doi: 10.1073/pnas.83.11.4040.

Abstract

The relationship of the neurofibrillary tangle, found in Alzheimer disease and aged brains, to normal or abnormal cytoskeletal proteins remains elusive. Although immunohistochemical studies have yielded disparate results, most antigenic determinants localized to neurofibrillary tangles are cytoskeletal constituents normally present in neuronal perikarya or dendrites. We report light and electron microscopic immunolabeling of neurofibrillary tangles by a monoclonal antibody to the microtubule-associated protein tau (tau). Dephosphorylation of tissue slices not only increased the number of tau-positive tangles but also produced marked positive immunoreactivity of neuritic plaques. The localization of tau, an axonal protein, to neurofibrillary tangles in the perikaryon in particular suggests that abnormal synthesis, modification, or aggregation of tau may induce aberrant cytoskeletal--cell organelle interactions, subsequent interference with axonal flow, and resultant tangle formation.

摘要

在阿尔茨海默病和老年大脑中发现的神经原纤维缠结与正常或异常细胞骨架蛋白之间的关系仍然难以捉摸。尽管免疫组织化学研究得出了不同的结果,但大多数定位于神经原纤维缠结的抗原决定簇是通常存在于神经元胞体或树突中的细胞骨架成分。我们报告了用一种针对微管相关蛋白tau(tau)的单克隆抗体对神经原纤维缠结进行光镜和电镜免疫标记的情况。组织切片的去磷酸化不仅增加了tau阳性缠结的数量,还使神经炎性斑块产生了明显的阳性免疫反应。tau作为一种轴突蛋白,尤其定位于胞体中的神经原纤维缠结,这表明tau的异常合成、修饰或聚集可能会诱导异常的细胞骨架 - 细胞器相互作用,随后干扰轴突运输,并导致缠结形成。

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