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应激状态下高迁移率族蛋白B1(HMGB1)的表型作用得以揭示。

High mobility group box 1 (HMGB1) phenotypic role revealed with stress.

作者信息

Tang Daolin, Kang Rui, Van Houten Bennett, Zeh Herbert J, Billiar Timothy R, Lotze Michael T

机构信息

Department of Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

Department of Pharmacology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America Department of Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

出版信息

Mol Med. 2014 Aug 19;20(1):359-62. doi: 10.2119/molmed.2014.00063.

Abstract

High mobility group box 1 (HMGB1) is an evolutionarily ancient protein that is present in one form or another in all eukaryotes. It fundamentally resides in the nucleus but translocates to the cytosol with stress and is subsequently released into the extracellular space. HMGB1 global knockout mice exhibit lethal hypoglycemia, whereas tissues and cells from conditional knockout or knock-in mice are born alive without apparent significant functional deficit. An aberrant response to targeted stress in the liver, pancreas, heart or myeloid cells is consistent with a protective role for HMGB1 in sustaining nuclear homeostasis and enabling other stress responses, including autophagy. Under some conditions, HMGB1 is not required for liver and heart function. Many challenges remain with respect to understanding the multiple roles of HMGB1 in health and disease.

摘要

高迁移率族蛋白B1(HMGB1)是一种进化上古老的蛋白质,在所有真核生物中都以某种形式存在。它主要存在于细胞核中,但在应激时会转移到细胞质中,随后释放到细胞外空间。HMGB1基因完全敲除的小鼠表现出致死性低血糖,而条件性敲除或敲入小鼠的组织和细胞出生时存活,没有明显的显著功能缺陷。肝脏、胰腺、心脏或髓样细胞对靶向应激的异常反应与HMGB1在维持核稳态和促进包括自噬在内的其他应激反应中的保护作用一致。在某些情况下,肝脏和心脏功能不需要HMGB1。在理解HMGB1在健康和疾病中的多种作用方面,仍存在许多挑战。

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