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阿尔茨海默病神经元中截短型tau蛋白与DNA片段化的共定位

Co-localization of truncated tau and DNA fragmentation in Alzheimer's disease neurones.

作者信息

Ugolini G, Cattaneo A, Novak M

机构信息

International School for Advanced Studies (SISSA), Neuroscience Programme, Trieste, Italy.

出版信息

Neuroreport. 1997 Dec 1;8(17):3709-12. doi: 10.1097/00001756-199712010-00010.

Abstract

Monoclonal antibody MN423 stains all hallmarks of tau neurofibrillary pathology in Alzheimer's disease (AD), without reacting with full-length tau. It recognizes tau molecules which are cleaved at Glu-391, suggesting that tau is endogenously truncated in AD brains. We investigated whether truncation of tau takes place in pre-tangle neurones. Our results showed that tau truncation occurs inside AD neurones in the absence of other signs of AD neurofibrillary pathology. Using in situ end labelling (ISEL) of DNA we found evidence for DNA fragmentation in a significant subpopulation of MN423-positive neurones. Our results therefore suggest that tau truncation is an early intracellular event preceding cell death in AD.

摘要

单克隆抗体MN423可标记阿尔茨海默病(AD)中tau神经原纤维病变的所有特征,且不与全长tau发生反应。它识别在Glu-391处被切割的tau分子,这表明在AD大脑中tau是内源性截短的。我们研究了tau截短是否发生在缠结前神经元中。我们的结果表明,在没有AD神经原纤维病变其他迹象的情况下,tau截短发生在AD神经元内部。通过DNA原位末端标记(ISEL),我们在大量MN423阳性神经元亚群中发现了DNA片段化的证据。因此,我们的结果表明,tau截短是AD中细胞死亡之前的早期细胞内事件。

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