蛋白磷酸酶在阿尔茨海默病及其他神经退行性疾病中的分子作用

Molecular Role of Protein Phosphatases in Alzheimer's and Other Neurodegenerative Diseases.

作者信息

Hassan Mubashir, Yasir Muhammad, Shahzadi Saba, Chun Wanjoo, Kloczkowski Andrzej

机构信息

The Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43205, USA.

Department of Pharmacology, Kangwon National University School of Medicine, Chuncheon 24341, Republic of Korea.

出版信息

Biomedicines. 2024 May 15;12(5):1097. doi: 10.3390/biomedicines12051097.

Abstract

Alzheimer's disease (AD) is distinguished by the gradual loss of cognitive function, which is associated with neuronal loss and death. Accumulating evidence supports that protein phosphatases (PPs; PP1, PP2A, PP2B, PP4, PP5, PP6, and PP7) are directly linked with amyloid beta (Aβ) as well as the formation of the neurofibrillary tangles (NFTs) causing AD. Published data reported lower PP1 and PP2A activity in both gray and white matters in AD brains than in the controls, which clearly shows that dysfunctional phosphatases play a significant role in AD. Moreover, PP2A is also a major causing factor of AD through the deregulation of the tau protein. Here, we review recent advances on the role of protein phosphatases in the pathology of AD and other neurodegenerative diseases. A better understanding of this problem may lead to the development of phosphatase-targeted therapies for neurodegenerative disorders in the near future.

摘要

阿尔茨海默病(AD)的特征是认知功能逐渐丧失,这与神经元的丧失和死亡有关。越来越多的证据支持蛋白磷酸酶(PPs;PP1、PP2A、PP2B、PP4、PP5、PP6和PP7)与β淀粉样蛋白(Aβ)以及导致AD的神经原纤维缠结(NFTs)的形成直接相关。已发表的数据报告称,与对照组相比,AD患者大脑灰质和白质中的PP1和PP2A活性均较低,这清楚地表明功能失调的磷酸酶在AD中起重要作用。此外,PP2A也是通过tau蛋白失调导致AD的主要因素。在这里,我们综述了蛋白磷酸酶在AD和其他神经退行性疾病病理学中的作用的最新进展。对这一问题的更好理解可能会在不久的将来促成针对神经退行性疾病的磷酸酶靶向治疗的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a29/11117500/366c57f317a0/biomedicines-12-01097-g001.jpg

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