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解析阿尔茨海默病和帕金森病中的 Tau 蛋白病。

Untangling the Tauopathy for Alzheimer's disease and parkinsonism.

机构信息

Department of Medical Science, Institute of Systems Neuroscience, 101, Section 2, Kuang-Fu Road, Hsinchu, 30013, Taiwan.

Brain Research Center, National Tsing Hua University, 101, Section 2, Kuang-Fu Road, Hsinchu, 30013, Taiwan.

出版信息

J Biomed Sci. 2018 Jul 10;25(1):54. doi: 10.1186/s12929-018-0457-x.

Abstract

Tau is a microtubule-associated protein that mainly localizes to the axon to stabilize axonal microtubule structure and neuronal connectivity. Tau pathology is one of the most common proteinopathies that associates with age-dependent neurodegenerative diseases including Alzheimer's disease (AD), and various Parkinsonism. Tau protein undergoes a plethora of intra-molecular modifications and some altered forms promote the production of toxic oligomeric tau and paired helical filaments, and through which further assemble into neurofibrillary tangles, also known as tauopathy. In this review, we will discuss the recent advances of the tauopathy research, primarily focusing on its association with the early axonal manifestation of axonal transport defect, axonal mitochondrial stress, autophagic vesicle accumulation and the proceeding of axon destruction, and the pathogenic Tau spreading across the synapse. Two alternative strategies either by targeting tau protein itself or by improving the age-related physiological decline are currently racing to find the hopeful treatment for tauopathy. Undoubtedly, more studies are needed to combat this devastating condition that has already affected millions of people in our aging population.

摘要

tau 是一种微管相关蛋白,主要定位于轴突,以稳定轴突微管结构和神经元连接。tau 病理学是与年龄相关的神经退行性疾病(包括阿尔茨海默病(AD)和各种帕金森病)相关的最常见的蛋白病之一。tau 蛋白经历了大量的分子内修饰,一些改变的形式促进了毒性寡聚 tau 和双螺旋丝的产生,通过这些进一步组装成神经原纤维缠结,也称为 tau 病。在这篇综述中,我们将讨论 tau 病研究的最新进展,主要集中在它与轴突运输缺陷、轴突线粒体应激、自噬囊泡积累和轴突破坏的早期轴突表现、以及穿过突触的致病性 Tau 扩散的关联上。目前有两种替代策略,一种是针对 tau 蛋白本身,另一种是改善与年龄相关的生理衰退,正在竞相寻找治疗 tau 病的有希望的方法。毫无疑问,需要更多的研究来对抗这种已经影响到我们老龄化人口中数百万人的破坏性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7448/6038292/75c400935b22/12929_2018_457_Fig1_HTML.jpg

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