Department of Biochemistry and Molecular Biology, School of Medicine, Nantong University, Nantong, 226001, China.
Co-innovation Center of Neuroregeneration, Key Laboratory of Neuroregeneration and Ministry of Education of Jiangsu, Nantong, 226001, China.
Curr Med Sci. 2020 Dec;40(6):1009-1021. doi: 10.1007/s11596-020-2282-1. Epub 2021 Jan 11.
Alzheimer's disease (AD) is an age-related neurodegenerative disease with two major hallmarks: extracellular amyloid plaques made of amyloid-β (Aβ) and intracellular neurofibrillary tangles (NFTs) of abnormally hyperphosphorylated tau. The number of NFTs correlates positively with the severity of dementia in AD patients. However, there is still no efficient therapy available for AD treatment and prevention so far. A deeper understanding of AD pathogenesis has identified novel strategies for the generation of specific therapies over the past few decades. Several studies have suggested that the prion-like seeding and spreading of tau pathology in the brain may be a key driver of AD. Tau protein is considered as a promising candidate target for the development of therapeutic interventions due to its considerable pathological role in a variety of neurodegenerative disorders. Abnormal tau hyperphosphorylation plays a detrimental pathological role, eventually leading to neurodegeneration. In the present review, we describe the recent research progresses in the pathological mechanisms of tau protein in AD and briefly discuss tau-based therapeutic strategies.
阿尔茨海默病(AD)是一种与年龄相关的神经退行性疾病,具有两个主要特征:由淀粉样蛋白-β(Aβ)组成的细胞外淀粉样斑块和异常过度磷酸化的 tau 组成的细胞内神经原纤维缠结(NFTs)。NFTs 的数量与 AD 患者痴呆的严重程度呈正相关。然而,迄今为止,AD 的治疗和预防仍没有有效的方法。对 AD 发病机制的深入了解在过去几十年中为特定疗法的产生确定了新的策略。几项研究表明,tau 病理学在大脑中的类朊病毒样播种和传播可能是 AD 的一个关键驱动因素。由于 tau 蛋白在多种神经退行性疾病中具有相当大的病理作用,因此它被认为是开发治疗干预措施的有前途的候选靶标。异常 tau 过度磷酸化发挥有害的病理作用,最终导致神经退行性变。在本综述中,我们描述了 AD 中 tau 蛋白病理机制的最新研究进展,并简要讨论了基于 tau 的治疗策略。