4.3 Review

Review: Therapeutic Targeting of HMGB1 in Stroke

期刊

CURRENT DRUG DELIVERY
卷 14, 期 6, 页码 785-790

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1567201813666160808111933

关键词

Cerebral ischemia; HMGB1; ICH; inflammation; RAGE; redox modification; SAH; stroke recovery; TLR4

资金

  1. Suzhou Key Medical Center [Szzx201501]
  2. National Natural Science Foundation of China [81571115, 81422013, 81471196]
  3. Scientific Department of Jiangsu Province [BL2014045]
  4. Suzhou Government [LCZX201301, SZS201413, SYS201332]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions

向作者/读者索取更多资源

High mobility group box-1 (HMGB1) is a nuclear protein that is expressed in almost all eukaryotic cells. In the nucleus, it maintains nuclear homeostasis and promotes gene transcription. HMGB1 can be passively released into the extracellular milieu after cell necrosis or actively secreted by activated immune cells. HMGB1 has several receptors such as Toll-like receptor 2, Toll-like receptor 4, and the receptor for advanced glycation end products. After brain injury, HMGB1 is released early from neural cells and contributes to the initial stages of the inflammatory response. However, surprisingly, HMGB1 can mediate beneficial effects during the course of stroke recovery. The biphasic biological property of extracellular HMGB1 may be related to the redox modifications of its cysteine residues. This review discusses the emerging roles of HMGB1 in several stroke models, as well as its potential role as a therapeutic target for stroke patients.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据