Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents

被引:163
|
作者
Jouanne, Marie [1 ,2 ]
Rault, Sylvain [1 ,2 ]
Voisin-Chiret, Anne-Sophie [1 ,2 ]
机构
[1] Univ Caen Normandie, Caen, France
[2] UNICAEN, CERMN EA 4258, FR CNRS INC3M 3038, SF ICORE 4206, Blvd Becquerel, F-14032 Caen, France
关键词
Alzheimer's disease; Tau protein; Aggregation; Therapeutic agents; PAIRED HELICAL FILAMENTS; MICROTUBULE-STABILIZING AGENT; POSITRON-EMISSION-TOMOGRAPHY; AMYLOID-BETA-AGGREGATION; IN-VITRO; NEURODEGENERATIVE DISEASES; NEUROFIBRILLARY TANGLES; SPECTRAL ASSIGNMENT; MOLECULAR TWEEZERS; INHIBITOR THERAPY;
D O I
10.1016/j.ejmech.2017.07.070
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Alzheimer's Disease (AD) is a neurodegenerative brain disorder in which many biological dysfunctions are involved. Among them, two main types of lesions were discovered and widely studied: the amyloid plaques and the neurofibrillary tangles (NFTs). These two lesions are caused by the dysfunction and the accumulation of two proteins which are, respectively, the beta-amyloid peptide and the tau protein. The process that leads these two proteins to aggregate is complex and is the subject of current studies. After a brief description of the aggregation mechanisms, we will provide an overview of new therapeutic agents targeting the different dysfunctions and toxic species found during aggregation. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:153 / 167
页数:15
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