How is inflammation initiated? Individual influences of IL-1, IL-18 and HMGB1

被引:143
|
作者
Keyel, Peter A. [1 ]
机构
[1] Texas Tech Univ, Dept Biol Sci, Lubbock, TX 79409 USA
关键词
Inflammasome; Caspase-1; NLRP3; DAMP; GROUP BOX 1; NECROSIS-FACTOR-ALPHA; TRYPANOSOMA-CRUZI INFECTION; COLLAGEN-INDUCED ARTHRITIS; NATURAL-KILLER-CELL; NF-KAPPA-B; LEISHMANIA-MAJOR; IFN-GAMMA; PLASMODIUM-FALCIPARUM; VIRUS-INFECTION;
D O I
10.1016/j.cyto.2014.03.007
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
Pro-inflammatory cytokines are crucial for fighting infection and establishing immunity. Recently, other proteins, such as danger-associated molecular patterns (DAMPs), have also been appreciated for their role in inflammation and immunity. Following the formation and activation of multiprotein complexes, termed inflammasomes, two cytokines, IL-1 beta and IL-18, along with the DAMP High Mobility Group Box 1 (HMGB1), are released from cells. Although these proteins all lack classical secretion signals and are released by inflammasome activation, they each lead to different downstream consequences. This review examines how various inflammasomes promote the release of IL-1 beta 1, IL-18 and HMGB1 to combat pathogenic situations. Each of these effector molecules plays distinct roles during sterile inflammation, responding to viral, bacterial and parasite infection, and tailoring the innate immune response to specific threats. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:136 / 145
页数:10
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