Novel insights into RIPK1 as a promising target for future Alzheimer's disease treatment

被引:36
作者
Li, Shang
Qu, Lailiang
Wang, Xiaobing [1 ]
Kong, Lingyi [1 ]
机构
[1] China Pharmaceut Univ, Sch Tradit Chinese Pharm, Jiangsu Key Lab Bioact Nat Prod Res, Nanjing 210009, Peoples R China
关键词
Alzheimer 's disease; neuroinflammation; beta-amyloid; RIPK1; necroptosis; RIPK1 inhibitors discovery; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; MIXED LINEAGE KINASE; INTERACTING PROTEIN-1 RIP1; DOMAIN-LIKE PROTEIN; CELL-DEATH; A-BETA; AMYLOID-BETA; NLRP3; INFLAMMASOME; INDUCED NECROPTOSIS;
D O I
10.1016/j.pharmthera.2021.107979
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alzheimer's disease (AD) is an intractable neurodegenerative disease showing a clinical manifestation with memory loss, cognitive impairment and behavioral dysfunction. The predominant pathological characteristics of AD include neuronal loss, beta-amyloid (A beta) deposition and hyperphosphorylated Tau induced neurofibrillary tangles (NFTs), while considerable studies proved these could be triggered by neuronal death and neuroinflam-mation. Receptor-interacting protein kinase 1 (RIPK1) is a serine/threonine kinase existed at the cross-point of cell death and inflammatory signaling pathways. Emerging investigations have shed light on RIPK1 for its potential role in AD progression. The present review makes a bird's eye view on the functions of RIPK1 and mainly focus on the underlying linkages between RIPK1 and AD from comprehensive aspects including neuronal death, A beta and Tau, inflammasome activation, BBB rupture, AMPK/mTOR, mitochondrial dysfunction and O-glcNAcylation. Moreover, the discovery of RIPK1 inhibitors, ongoing clinical trials along with future RIPK1-targeted therapeutics are also reviewed. (C) 2021 Elsevier Inc. All rights reserved.
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页数:16
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