Pyroptosis as a candidate therapeutic target for Alzheimer's disease

被引:12
|
作者
Huang, Yuehua [1 ,2 ]
Li, Xiaoyu [3 ]
Luo, Guifei [1 ,2 ]
Wang, Junli [2 ,4 ]
Li, Ranhui [3 ]
Zhou, Chuyi [3 ]
Wan, Teng [3 ]
Yang, Fenglian [4 ]
机构
[1] Youjiang Med Univ Nationalities, Affiliated Hosp, Dept Reprod Med, Baise, Guangxi, Peoples R China
[2] Youjiang Med Univ Nationalities, Affiliated Hosp, Guangxi Med & Hlth Key Discipline Construct Projec, Reprod Med, Baise, Guangxi, Peoples R China
[3] Univ South China, Hengyang Med Coll, Hengyang, Hunan, Peoples R China
[4] Youjiang Med Univ Nationalities, Ind Coll Biomed & Hlth Ind, Baise, Guangxi, Peoples R China
来源
FRONTIERS IN AGING NEUROSCIENCE | 2022年 / 14卷
关键词
Alzheimer's disease; pyroptosis; amyloid beta; tau; neuroinflammation; INFLAMMATORY CASPASES; NLRP1; INFLAMMASOME; GASDERMIN D; CELL-DEATH; MICROGLIA; BETA; INTERLEUKIN-1; MODEL;
D O I
10.3389/fnagi.2022.996646
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Pyroptosis is a form of cell death mediated by inflammasomes and gasdermins, and the relevance of pyroptosis to neurodegenerative diseases is currently receiving increasing attention. Alzheimer's disease (AD) is a chronic progressive neurodegenerative disease that is closely associated with neuroinflammation. Its main pathological features include beta-amyloid (A beta) deposition, Tau protein hyperphosphorylation and neuronal loss. A beta, tau-induced microglia pyroptosis and polarization leading to neuroinflammation play an important role in the pathogenesis of AD. Studying the pathogenesis and treatment of AD based on cellular pyroptosis has become a new direction in AD research. In this paper, we review the research progress of pyroptosis and will focus on the pathogenic roles of pyroptosis in AD and the role of targeted inhibition of inflammasome-dependent pyroptosis in AD treatment. These results deepen our understanding of the pathogenesis of AD and provide ideas for the development of new drugs based on the regulation of pyroptosis in AD patients.
引用
收藏
页数:11
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