Zhou Jian-guang, Zheng Min
Department of Dermatology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2007 Jul;36(4):412-6. doi: 10.3785/j.issn.1008-9292.2007.04.019.
High mobility group box chromosomal protein 1 (HMGB1) is originally identified as a DNA-binding protein that functions as a structural co-factor. HMGB1 is actively secreted by macrophage/monocytes via inflammatory stimuli. The extracellular HMGB-1 acts as a mediator of acute and chronic systematic inflammation. In this article we briefly review its role in rheumatic diseases: arthritis, polymyositis and dermatomyositis, lupus erythematosus and Sjogren's syndrome. Increased cytoplasmic expression and extracellular deposition of HMGB1 are found in the affected tissues of those diseases, especially stronger in/around focal infiltrates of mononuclear cells. TNFalpha and IL-1beta are co-expressed in areas of extracellular HMGB1. HMGB1 together with TNF alpha and IL-1beta may form a proinflammatory loop promoting the chronic inflammations. The new findings of HMGB1 as a cytokine provide a better understanding of rheumatiod diseases, and could become a clinically relevant therapeutic target that might be more efficient than other known cytokines.
高迁移率族蛋白B1(HMGB1)最初被鉴定为一种作为结构辅助因子发挥作用的DNA结合蛋白。HMGB1通过炎症刺激由巨噬细胞/单核细胞主动分泌。细胞外HMGB-1作为急性和慢性全身炎症的介质。在本文中,我们简要回顾其在风湿性疾病中的作用:关节炎、多发性肌炎和皮肌炎、红斑狼疮和干燥综合征。在这些疾病的受累组织中发现HMGB1的细胞质表达增加和细胞外沉积,在单核细胞的局灶性浸润内/周围尤为明显。TNFα和IL-1β在细胞外HMGB1区域共表达。HMGB1与TNFα和IL-1β一起可能形成一个促炎环,促进慢性炎症。HMGB1作为一种细胞因子的新发现有助于更好地理解类风湿性疾病,并可能成为一个临床上相关的治疗靶点,可能比其他已知细胞因子更有效。