High-mobility group box 1 protein (HMGB1) operates as an alarmin outside as well as inside cells

被引:235
作者
Andersson, Ulf [1 ]
Yang, Huan [2 ]
Harris, Helena [3 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Ctr Mol Med CMM L8 04, Dept Womens & Childrens Hlth, S-17176 Stockholm, Sweden
[2] Feinstein Inst Med Res, Lab Biomed Sci, 350 Community Dr, Manhasset, NY 11030 USA
[3] Karolinska Univ Hosp, Karolinska Inst, Ctr Mol Med CMM L8 04, Unit Rheumatol,Dept Med, S-17176 Stockholm, Sweden
关键词
Alarmins; DAMPs; HMGB1; TLR4; RAGE; Inflammation; Trauma; Sepsis; NONCANONICAL INFLAMMASOME ACTIVATION; INDUCED LIVER-INJURY; ACUTE LUNG INJURY; POSTTRANSLATIONAL MODIFICATIONS; MECHANISTIC BIOMARKERS; RHEUMATOID-ARTHRITIS; SERUM-LEVELS; RECEPTOR; RAGE; BINDING;
D O I
10.1016/j.smim.2018.02.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alarmins are preformed, endogenous molecules that can be promptly released to signal cell or tissue stress or damage. The ubiquitous nuclear molecule high-mobility group box 1 protein (HMGB1) is a prototypical alarmin activating innate immunity. HMGB1 serves a dual alarmin function. The protein can be emitted to alert adjacent cells about endangered homeostasis of the HMGB1-releasing cell. In addition to this expected path of an alarmin, extracellular HMGB1 can be internalized via RAGE-receptor mediated endocytosis to the endolysosomal compartment while attached to other extracellular proinflammatory molecules. The endocytosed HMGB1 may subsequently destabilize lysosomal membranes. The HMGB1-bound partner molecules depend on the HMGB1-mediated transport and the induced lysosomal leakage to obtain access to endosomal and cytosolic reciprocal sensors to communicate extracellular threat and to initiate the proper activation pathways.
引用
收藏
页码:40 / 48
页数:9
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