Location is the key to function: HMGB1 in sepsis and trauma-induced inflammation

被引:162
作者
Deng, Meihong [1 ,2 ]
Scott, Melanie J. [1 ,2 ,3 ]
Fan, Jie [1 ,2 ,4 ]
Billiar, Timothy R. [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Surg, F1281 PUH,200 Lothrop St, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Pittsburgh Trauma Res Ctr, Pittsburgh, PA USA
[3] Univ Pittsburgh, Pittsburgh Liver Res Ctr, Pittsburgh, PA USA
[4] Vet Affairs Pittsburgh Healthcare Syst, Res & Dev, Pittsburgh, PA USA
关键词
AIM2; autophagy; caspase-11; DAMPs; pyroptosis; GROUP BOX-1 PROTEIN; ENDOTHELIAL-CELLS; HEMORRHAGIC-SHOCK; CYTOKINE ACTIVITY; PLATELET HMGB1; DNA-BINDING; MOBILITY; ACTIVATION; RELEASE; DYSFUNCTION;
D O I
10.1002/JLB.3MIR1218-497R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
High mobility group box 1 (HMGB1) is a multifunctional nuclear protein, probably known best as a prototypical alarmin or damage-associated molecular pattern (DAMP) molecule when released from cells. However, HMGB1 has multiple functions that depend on its location in the nucleus, in the cytosol, or extracellularly after either active release from cells, or passive release upon lytic cell death. Movement of HMGB1 between cellular compartments is a dynamic process induced by a variety of cell stresses and disease processes, including sepsis, trauma, and hemorrhagic shock. Location of HMGB1 is intricately linked with its function and is regulated by a series of posttranslational modifications. HMGB1 function is also regulated by the redox status of critical cysteine residues within the protein, and is cell-type dependent. This review highlights some of the mechanisms that contribute to location and functions of HMGB1, and focuses on some recent insights on important intracellular effects of HMGB1 during sepsis and trauma.
引用
收藏
页码:161 / 169
页数:9
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