Molecular mechanisms of necroptosis and relevance for neurodegenerative diseases

被引:31
作者
Dionisio, Pedro A. [1 ]
Amaral, Joana D. [1 ]
Rodrigues, Cecilia M. P. [1 ]
机构
[1] Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
来源
CELL DEATH REGULATION IN HEALTH AND DISEASE - PT C | 2020年 / 353卷
关键词
TUMOR-NECROSIS-FACTOR; MIXED LINEAGE KINASE; A20 RESTRICTS UBIQUITINATION; TNF-INDUCED-NECROPTOSIS; SPINAL-CORD-INJURY; SHOCK-PROTEIN; 90; CELL-DEATH; KAPPA-B; PROGRAMMED NECROSIS; DOMAIN-LIKE;
D O I
10.1016/bs.ircmb.2019.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Necroptosis is a regulated cell death pathway morphologically similar to necrosis that depends on the kinase activity of receptor interacting protein 3 (RIP3) and the subsequent activation of the pseudokinase mixed lineage kinase domain-like protein (MLKL), being also generally dependent on RIP1 kinase activity. Necroptosis can be recruited during pathological conditions, usually following the activation of death receptors under specific cellular contexts. In this regard, necroptosis has been implicated in the pathogenesis of multiple disorders, including acute and chronic neurodegenerative diseases, such as Parkinson's and Alzheimer's diseases, and multiple sclerosis. Here, we summarize the molecular mechanisms regulating the induction of necroptosis and downstream effectors of this form of cell death, besides exploring non-necroptotic roles for necroptosis-related proteins that may impact on alternative cell death pathways and inflammatory mechanisms in disease. Finally, we outline the recent evidence implicating necroptosis in neurodegenerative conditions and the emerging therapeutic perspectives targeting necroptosis in these diseases.
引用
收藏
页码:31 / 82
页数:52
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