Department of Surgery Intensive Care Unit, Affiliated Ruijin Hospital of Medical College of Shanghai Jiaotong University, Shanghai 200025, China.
Cytokine. 2010 Aug;51(2):119-26. doi: 10.1016/j.cyto.2010.02.021. Epub 2010 Mar 26.
High-mobility group box 1 (HMGB1), a highly conserved protein previously known as a DNA-binding protein involved in maintenance of nucleosome structure and regulation of gene transcription, was recently found to act as a potent proinflammatory cytokine during infection responses. Levels of HMGB1 increase in serum and tissues during infection, especially in sepsis. Sepsis, which is a systemic inflammatory response disease, is the most severe complication of infection and is a deadly disease, and HMGB1 acting as a potent proinflammatory cytokine involve in the delayed endotoxin lethality and systemic inflammatory response. A growing number of studies have demonstrated HMGB1 is a cytokine that can mediate inflammation and is a potential therapeutic target in experimental models of sepsis. To reduce sepsis-related mortality, a better understanding of HMGB1 is essential. In this article, we will describe the structure, release process, intracellular function, and cell surface receptors of HMGB1, but will primarily focus on its extracellular roles and mechanism in inflammation, especially in sepsis.
高迁移率族蛋白 B1(HMGB1)是一种高度保守的蛋白质,先前被认为是一种 DNA 结合蛋白,参与核小体结构的维持和基因转录的调节。最近在感染反应中发现,它作为一种有效的促炎细胞因子发挥作用。在感染过程中,HMGB1 在血清和组织中的水平升高,特别是在败血症中。败血症是一种全身性炎症反应疾病,是感染最严重的并发症,也是一种致命的疾病,而作为一种有效的促炎细胞因子的 HMGB1 参与了延迟内毒素致死和全身性炎症反应。越来越多的研究表明,HMGB1 是一种能够介导炎症的细胞因子,是败血症实验模型中潜在的治疗靶点。为了降低与败血症相关的死亡率,必须更好地了解 HMGB1。本文将描述 HMGB1 的结构、释放过程、细胞内功能和细胞表面受体,但主要将重点放在其在炎症,特别是败血症中的细胞外作用和机制上。