Regulated cell death and inflammation: an auto-amplification loop causes organ failure

被引:503
作者
Linkermann, Andreas [1 ]
Stockwell, Brent R. [2 ,3 ]
Krautwald, Stefan [1 ]
Anders, Hans-Joachim [4 ]
机构
[1] Univ Kiel, Clin Nephrol & Hypertens, D-24105 Kiel, Germany
[2] Columbia Univ, Dept Biol Sci, Dept Chem, New York, NY 10027 USA
[3] Columbia Univ, Howard Hughes Med Inst, New York, NY 10027 USA
[4] Klinikum LMU, Med Klin & Poliklin 4, D-80336 Munich, Germany
基金
美国国家卫生研究院;
关键词
MIXED LINEAGE KINASE; MITOCHONDRIAL PERMEABILITY TRANSITION; CYCLOPHILIN-D; DOMAIN-LIKE; MEDIATES NECROPTOSIS; PROGRAMMED NECROSIS; NALP3; INFLAMMASOME; IMMUNE-RESPONSE; RIP1; KINASE; PYROPTOSIS;
D O I
10.1038/nri3743
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Regulated cell death (RCD) is either immunologically silent or immunogenic. RCD in parenchymal cells may lead to the release of damage-associated molecular patterns that drive both tissue inflammation and the activation of further pathways of RCD. Following an initial event of regulated necrosis, RCD and inflammation can induce each other and drive a local auto-amplification loop that leads to exaggerated cell death and inflammation. In this Opinion article, we propose that such crosstalk between pro-inflammatory and RCD pathways has pathophysiological relevance in solid organ failure, transplantation and cancer. In our opinion, clinicians should not only prescribe immunosuppressive treatments to disrupt this circuit, but also implement the neglected therapeutic option of adding compounds that interfere with RCD.
引用
收藏
页码:759 / 767
页数:9
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