脑可溶性Tau蛋白及其分泌因子的定量分析

Pengcheng Han, G. Serrano, T. Beach, R. Caselli, Junxiang Yin, Ningning Zhuang, Jiong Shi
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引用次数: 31

摘要

神经原纤维缠结(nft)是阿尔茨海默病(AD)患者大脑中不溶性tau蛋白的产物。脑脊液(CSF) tau水平是AD诊断的生物标志物。脑实质中tau蛋白的可溶部分可能是脑脊液tau蛋白的来源,但此前尚未对其进行量化。我们在尸检中测量了7名认知正常、12名轻度认知受损和19名AD受试者的颞叶和额叶脑组织样本的脑脊液tau和可溶性脑tau。基于测量的脑可溶性tau,我们计算了全脑tau负荷并估计了tau分泌因子。我们的研究结果表明,AD中NFT的增加可能归因于翻译后过程;阿尔茨海默病患者脑脊液tau蛋白的增加是由于基于载体的分泌加速。此外,通过最终迷你精神状态检查评分评估的认知功能障碍与分泌因子相关,但与可溶性tau蛋白无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Quantitative Analysis of Brain Soluble Tau and the Tau Secretion Factor
Neurofibrillary tangles (NFTs) represent products of insoluble tau protein in the brains of patients with Alzheimer disease (AD). The cerebrospinal fluid (CSF) tau level is a biomarker in AD diagnosis. The soluble portion of tau protein in brain parenchyma is presumably the source for CSF tau but this has not previously been quantified. We measured CSF tau and soluble brain tau at autopsy in temporal and frontal brain tissue samples from 7 cognitive normal, 12 mild cognitively impaired, and 19 AD subjects. Based on the measured brain soluble tau, we calculated the whole brain tau load and estimated tau secretion factor. Our results suggest that the increase in NFT in AD is likely attributable to post-translational processes; the increase in CSF tau in AD patients is due to an accelerated carrier-based secretion. Moreover, cognitive dysfunction assessed by final Mini-Mental State Examination scores correlated with the secretion factor but not with the soluble tau.
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