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细胞激活和细胞死亡过程中高迁移率族蛋白B1(HMGB1)的易位。

The translocation of HMGB1 during cell activation and cell death.

作者信息

Gauley Julie, Pisetsky David S

机构信息

Division of Rheumatology & Immunology, Duke University Medical Center, Durham, NC 27705, USA.

出版信息

Autoimmunity. 2009 May;42(4):299-301. doi: 10.1080/08916930902831522.

Abstract

High-mobility group box protein 1 (HMGB1) is a non-histone nuclear protein with alarmin activity. When present in an extracellular location, HMGB1 can activate the innate immune system and promote inflammation in conditions such as sepsis. To exert these activities, HMGB1 must transit from the nucleus, through the cytoplasm, to the outside of the cell. This process can occur during cell activation as well as cell death. In murine macrophages (MPhi), stimulation of TLR3 and TLR4, but not TLR9, can cause HMGB1 translocation. With cell death, necrosis can lead to extracellular HMGB1 by a passive mechanism. With apoptosis, HMGB1 is only released during secondary necrosis, when cell permeability barriers break down. Since agents that stimulate MPhi can also induce apoptosis, HMGB1 release following TLR stimulation may also reflect a contribution from dead cells, suggesting a common mechanism for protein release in activation and death.

摘要

高迁移率族蛋白B1(HMGB1)是一种具有警报素活性的非组蛋白核蛋白。当处于细胞外位置时,HMGB1可激活先天免疫系统,并在脓毒症等病症中促进炎症反应。为发挥这些活性,HMGB1必须从细胞核穿过细胞质转运至细胞外。此过程可发生在细胞激活以及细胞死亡期间。在小鼠巨噬细胞(MPhi)中,TLR3和TLR4的刺激而非TLR9的刺激可导致HMGB1易位。细胞死亡时,坏死可通过被动机制导致细胞外HMGB1的出现。细胞凋亡时,HMGB1仅在继发性坏死期间释放,此时细胞通透性屏障瓦解。由于刺激MPhi的因子也可诱导细胞凋亡,TLR刺激后HMGB1的释放也可能反映了死亡细胞的作用,提示了激活和死亡过程中蛋白质释放的共同机制。

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