Pyroptosis versus necroptosis: similarities, differences, and crosstalk

被引:770
|
作者
Frank, Daniel [1 ,2 ]
Vince, James E. [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, 1G Royal Parade, Melbourne, Vic 3052, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic 3050, Australia
来源
CELL DEATH AND DIFFERENTIATION | 2019年 / 26卷 / 01期
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
NLRP3 INFLAMMASOME ACTIVATION; MIXED LINEAGE KINASE; DOMAIN-LIKE PROTEIN; GASDERMIN-D PORE; CELL-DEATH; PLASMA-MEMBRANE; INTERLEUKIN-1-BETA MATURATION; MEDIATES NECROPTOSIS; PSEUDOKINASE MLKL; EAT-ME;
D O I
10.1038/s41418-018-0212-6
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
Pyroptosis and necroptosis represent two pathways of genetically encoded necrotic cell death. Although these cell death programmes can protect the host against microbial pathogens, their dysregulation has been implicated in a variety of autoimmune and auto-inflammatory conditions. The disease-promoting potential of necroptosis and pyroptosis is likely a consequence of their ability to induce a lytic cell death. This cell suicide mechanism, distinct from apoptosis, allows the release of immunogenic cellular content, including damage-associated molecular patterns (DAMPs), and inflammatory cytokines such as interleukin-1 beta (IL-1 beta), to trigger inflammation. In this Review, we discuss recent discoveries that have advanced our understanding on the primary functions of pyroptosis and necroptosis, including evidence for the specific cytokines and DAMPs responsible for driving inflammation. We compare the similar and unique aspects of pyroptotic-and necroptotic-induced membrane damage, and explore how these may functionally impact distinct intracellular organelles and signalling pathways. We also examine studies highlighting the crosstalk that can occur between necroptosis and pyroptosis signalling, and evidence supporting the physiological significance of this convergence. Ultimately, a better understanding of the similarities, unique aspects and crosstalk of pyroptosis and necroptosis will inform as to how these cell death pathways might be manipulated for therapeutic benefit.
引用
收藏
页码:99 / 114
页数:16
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