Department of Physiology, Hunan Normal University Medical College, Changsha, Hunan, China (mainland).
Department of Pathology and Key Laboratory of Cancer Stem Cells and Translational Medicine, Hunan Normal University Medical College, Changsha, Hunan, Christmas island.
Med Sci Monit. 2019 Mar 11;25:1828-1837. doi: 10.12659/MSM.912867.
Acute lung injury (ALI) is a life-threatening clinical syndrome in critically ill patients. The identification of novel biological markers for the early diagnosis of ALI and the development of more effective treatments are topics of current research. High mobility group box-1 protein (HMGB1) is a late inflammatory mediator associated with sepsis, malignancy, and immune disease. Levels of HMGB1 may reflect the severity of inflammation and tissue damage, indicating a potential role for HMGB1 as a prognostic biomarker in ALI, and a potential target for blocking inflammatory pathways. Several studies have shown that HMGB1 regulates autophagy. Autophagy, or type II programmed cell death, is an essential biological process that maintains cellular homeostasis. Studies have shown that HMGB1 and autophagy are involved in the pathogenesis of many lung diseases including ALI but the specific mechanisms underlying this association remain to be determined. This review aims to provide an update on the current status of the role of HMBG1 and autophagy in ALI.
急性肺损伤(ALI)是危重病患者中一种危及生命的临床综合征。寻找用于 ALI 早期诊断的新型生物标志物和开发更有效的治疗方法是当前研究的主题。高迁移率族蛋白 B1(HMGB1)是一种与脓毒症、恶性肿瘤和自身免疫性疾病相关的晚期炎症介质。HMGB1 水平可能反映炎症和组织损伤的严重程度,表明 HMGB1 作为 ALI 预后生物标志物的潜在作用,以及作为阻断炎症途径的潜在靶点。一些研究表明,HMGB1 调节自噬。自噬或Ⅱ型程序性细胞死亡,是维持细胞内环境稳定的必要的生物学过程。研究表明,HMGB1 和自噬参与了许多肺部疾病包括 ALI 的发病机制,但这种关联的具体机制仍有待确定。本综述旨在提供关于 HMGB1 和自噬在 ALI 中的作用的最新研究现状。