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HMGB1 通过炎性小体释放。

HMGB1 release by inflammasomes.

机构信息

Department of Biochemistry, Ghent University, Ghent, Belgium.

出版信息

Virulence. 2011 Mar-Apr;2(2):162-5. doi: 10.4161/viru.2.2.15480. Epub 2011 Mar 1.

Abstract

High-mobility group box 1 (HMGB1) was originally identified as a highly conserved nuclear DNA-binding protein that participates in DNA replication, repair and transcriptional regulation of gene expression. Although the nuclear role of HMGB1 is not quite understood, recent studies characterized the emerging role of extracellular HMGB1 as a prototypical danger signal that regulates inflammatory and repair responses. Under conditions of infection, injury and sterile inflammation, HMGB1 can be passively released from damaged cells or actively secreted from activated immune cells. Inflammasomes, large caspase-1-activating protein complexes, were recently shown to play a critical role in mediating the extracellular release of HMGB1 from activated and infected immune cells.

摘要

高迁移率族蛋白 B1(HMGB1)最初被鉴定为一种高度保守的核 DNA 结合蛋白,参与 DNA 复制、修复和基因表达的转录调控。尽管 HMGB1 的核作用尚不完全清楚,但最近的研究描述了细胞外 HMGB1 作为一种典型的危险信号的新兴作用,该信号调节炎症和修复反应。在感染、损伤和无菌性炎症的情况下,HMGB1 可以从受损细胞中被动释放,或从激活的免疫细胞中主动分泌。最近的研究表明,炎性小体(一种大型的半胱氨酸蛋白酶-1 激活蛋白复合物)在介导激活和感染的免疫细胞中外泌 HMGB1 中发挥着关键作用。

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本文引用的文献

1
Emerging inflammasome effector mechanisms.新兴的炎症小体效应机制。
Nat Rev Immunol. 2011 Mar;11(3):213-20. doi: 10.1038/nri2936.
2
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J Immunol. 2010 Oct 1;185(7):4385-92. doi: 10.4049/jimmunol.1000803. Epub 2010 Aug 27.
4
Sensing and signaling in antiviral innate immunity.抗病毒先天免疫中的感应和信号转导。
Curr Biol. 2010 Apr 13;20(7):R328-33. doi: 10.1016/j.cub.2010.01.044.
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The inflammasomes.炎性小体
PLoS Pathog. 2009 Dec;5(12):e1000510. doi: 10.1371/journal.ppat.1000510. Epub 2009 Dec 24.
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IL-33 raises alarm.白细胞介素-33发出警报。
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