High-mobility group box 1 protein and its role in severe acute pancreatitis

被引:58
|
作者
Shen, Xiao [1 ]
Li, Wei-Qin [1 ]
机构
[1] Nanjing Univ, Sch Med, Jinling Hosp, Dept Gen Surg, Nanjing 210002, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
High mobility group box 1 protein; Inhibitors; Inflammation; Severe acute pancreatitis; Nuclear factor kappa B; NF-KAPPA-B; GLYCATION END-PRODUCTS; DISTANT ORGAN INJURY; TOLL-LIKE RECEPTORS; ACUTE LUNG INJURY; ETHYL PYRUVATE; ENDOTHELIAL-CELLS; TARGETING HMGB1; SEVERE SEPSIS; LATE MEDIATOR;
D O I
10.3748/wjg.v21.i5.1424
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The high mobility group box 1 (HMGB1), which belongs to the subfamily of HMG-1/-2, is a highly conserved single peptide chain consisting of 215 amino acid residues with a molecular weight of approximately 24894 Da. HMGB1 is a ubiquitous nuclear protein in mammals and plays a vital role in inflammatory diseases. Acute pancreatitis is one of the most common causes of acute abdominal pain with a poor prognosis. Acute pancreatitis is an acute inflammatory process of the pancreas (duration of less than six months), for which the severe form is called severe acute pancreatitis (SAP). More and more studies have shown that HMGB1 has a bidirectional effect in the pathogenesis of SAP. Extracellular HMGB1 can aggravate the pancreatic inflammatory process, whereas intracellular HMGB1 has a protective effect against pancreatitis. The mechanism of HMGB1 is multiple, mainly through the nuclear factor.B pathway. Receptors for advanced glycation endproducts and toll-like receptors (TLR), especially TLR-2 and TLR-4, are two major types of receptors mediating the inflammatory process triggered by HMGB1 and may be also the main mediators in the pathogenesis of SAP. HMGB1 inhibitors, such as ethyl pyruvate, pyrrolidine dithiocarbamate and Scolopendra subspinipes mutilans, can decrease the level of extracellular HMGB1 and are the promising targets in the treatment of SAP.
引用
收藏
页码:1424 / 1435
页数:12
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