A novel "complement-metabolism-inflammasome axis" as a key regulator of immune cell effector function

被引:122
作者
Arbore, Giuseppina [1 ]
Kemper, Claudia [1 ,2 ,3 ]
机构
[1] Kings Coll London, Div Transplant Immunol & Mucosal Biol, MRC Ctr Transplantat, London SE1 9RT, England
[2] NHLBI, Lab Mol Immunol, NIH, Bldg 10, Bethesda, MD 20892 USA
[3] NHLBI, Ctr Immunol, NIH, Bldg 10, Bethesda, MD 20892 USA
基金
英国惠康基金;
关键词
Complement; Metabolism; NLRP3; inflammasome; NLRP3; INFLAMMASOME; MEDIATED INFLAMMATION; IL-1-BETA SECRETION; PATTERN-RECOGNITION; CUTTING EDGE; IFN-GAMMA; T-CELLS; ACTIVATION; RECEPTOR; CYTOKINE;
D O I
10.1002/eji.201546131
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
The inflammasomes are intracellular multiprotein complexes that induce and regulate the generation of the key pro-inflammatory cytokines IL-1 beta and IL-18 in response to infectious microbes and cellular stress. The activation of inflammasomes involves several upstream signals including classic pattern or danger recognition systems such as the TLRs. Recently, however, the activation of complement receptors, such as the anaphylatoxin C3a and C5a receptors and the complement regulator CD46, in conjunction with the sensing of cell metabolic changes, for instance increased amino acid influx and glycolysis (via mTORC1), have emerged as additional critical activators of the inflammasome. This review summarizes recent advances in our knowledge about complement-mediated inflammasome activation, with a specific focus on a novel " complement - metabolism - NLRP3 inflammasome axis."
引用
收藏
页码:1563 / 1573
页数:11
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