进行性核上麻痹
皮质基底变性
陶氏病
τ蛋白
失智症
神经退行性变
神经科学
Tau病理学
帕金森病
疾病
医学
生物
阿尔茨海默病
痴呆
病理
作者
Yong-Lei Gao,Nan Wang,Fu-Rong Sun,Xi‐Peng Cao,Wei Zhang,Jin‐Tai Yu
出处
期刊:Annals of Translational Medicine
[AME Publishing Company]
日期:2018-05-01
卷期号:6 (10): 175-175
被引量:172
标识
DOI:10.21037/atm.2018.04.23
摘要
Tau, a microtubule-associated protein, is the main component of the intracellular filamentous inclusions that are involved in neurodegenerative diseases known as tauopathies, including Alzheimer disease (AD), frontotemporal dementia with parkinsonism-17 (FTDP-17), Pick disease (PiD), progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). Hyperphosphorylated, aggregated tau proteins form the core of neurofibrillary tangles (NFTs), which are shown to be one of the pathological hallmarks of AD. The discovery of mutations in the microtubule-associated protein tau (MAPT) gene in patients with FTDP-17 also contributes to a better understanding of the dysfunctional tau as a cause of diseases. Although recent substantial progress has been made in the tau pathology of tauopathies, the mechanisms underlying tau-induced neurodegeneration remain unclear. Here, we present an overview of the biochemical properties of tau protein and the pathogenesis underlying tau-induced neurodegenerative diseases. Meanwhile, we will discuss the tau-related biomarkers and ongoing tau-targeted strategies for therapeutic modulation.
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