The Role and Pathogenesis of Tau Protein in Alzheimer's Disease.

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomolecules Pub Date : 2025-06-05 DOI:10.3390/biom15060824
Xiaoyue Hong, Linshu Huang, Fang Lei, Tian Li, Yi Luo, Mengliu Zeng, Zhuo Wang
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Abstract

Alzheimer's disease (AD), a predominant neurodegenerative disorder, is clinically characterized by progressive cognitive deterioration and behavioral deficits. An in-depth understanding of the pathogenesis and neuropathology of AD is essential for the development of effective treatments and early diagnosis techniques. The neuropathological signature of AD involves two hallmark lesions: intraneuronal neurofibrillary tangles composed of hyperphosphorylated tau aggregates and extracellular senile plaques containing amyloid-β (Aβ) peptide depositions. Although Aβ-centric research has dominated AD investigations over the past three decades, pharmacological interventions targeting Aβ pathology have failed to demonstrate clinical efficacy. Tau, a microtubule-associated protein predominantly localized to neuronal axons, orchestrates microtubule stabilization and axonal transport through dynamic tubulin interactions under physiological conditions. In AD pathogenesis, however, tau undergoes pathogenic post-translational modifications (PTMs), encompassing hyperphosphorylation, lysine acetylation, methylation, ubiquitination, and glycosylation. These PTM-driven alterations induce microtubule network disintegration, mitochondrial dysfunction, synaptic impairment, and neuroinflammatory cascades, ultimately culminating in irreversible neurodegeneration and progressive cognitive decline. This review synthesizes contemporary advances in tau PTM research and delineates their mechanistic contributions to AD pathogenesis, thereby establishing a framework for biomarker discovery, targeted therapeutic development, and precision medicine approaches in tauopathies. This review synthesizes contemporary advances in tau PTM research and delineates their mechanistic contributions to AD pathogenesis, thereby establishing a solid theoretical and experimental basis for the early diagnosis of neurodegenerative diseases, the discovery of therapeutic targets, and the development of novel therapeutic strategies.

Tau蛋白在阿尔茨海默病中的作用及其发病机制。
阿尔茨海默病(AD)是一种主要的神经退行性疾病,临床特征是进行性认知退化和行为缺陷。深入了解阿尔茨海默病的发病机制和神经病理学对于开发有效的治疗方法和早期诊断技术至关重要。阿尔茨海默病的神经病理学特征包括两个标志性病变:由过度磷酸化的tau聚集物组成的神经元内神经原纤维缠结和含有淀粉样蛋白-β (Aβ)肽沉积的细胞外老年斑。尽管以Aβ为中心的研究在过去三十年中主导了AD的研究,但针对Aβ病理的药物干预未能证明临床疗效。Tau是一种微管相关蛋白,主要定位于神经元轴突,在生理条件下通过动态微管蛋白相互作用协调微管稳定和轴突运输。然而,在AD发病机制中,tau蛋白经历了致病性翻译后修饰(PTMs),包括过磷酸化、赖氨酸乙酰化、甲基化、泛素化和糖基化。这些ptm驱动的改变诱导微管网络解体、线粒体功能障碍、突触损伤和神经炎症级联反应,最终导致不可逆的神经变性和进行性认知能力下降。本文综述了tau蛋白PTM研究的最新进展,并描述了它们在AD发病机制中的作用,从而为tau蛋白PTM的生物标志物发现、靶向治疗开发和精准医学方法建立了框架。本文综述了当前tau PTM的研究进展,阐述了其在AD发病机制中的作用,为神经退行性疾病的早期诊断、治疗靶点的发现和新的治疗策略的开发奠定了坚实的理论和实验基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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