[Serpins as important protective factors in the pathogenesis of acute lung injury/acute respiratory distress syndrome].

急性呼吸窘迫综合征 医学 蛋白酶3 组织蛋白酶G 发病机制 中性粒细胞弹性蛋白酶 免疫学 蛋白酵素 弥漫性肺泡损伤 炎症 髓过氧化物酶 内科学 急性呼吸窘迫 生物 生物化学
作者
Jinquan Zhang,Caiming Xu,Guixin Zhang,Yalan Luo,Peng Ge,Hailong Chen
出处
期刊:Chinese critical care medicine [Chinese Medical Association]
卷期号:33 (3): 368-372
标识
DOI:10.3760/cma.j.cn121430-20200922-00644
摘要

Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) is a common respiratory disease in clinic, and with a pathological manifestation of pulmonary edema, decreased pulmonary compliance as well as pulmonary epithelial/endothelial cells injury. At present, it was suggested that systemic inflammatory response syndrome (SIRS) caused by various causes which play an important role in the occurrence and development of ALI/ARDS. Widely activated neutrophils can migrate to lung tissue and release plenty of proteases in the procedure of SIRS, including neutrophil serine proteases (NSPs), lysozyme, myeloperoxidase and collagenase, which can induce severe lung injury. Meanwhile, NSPs, such as neutrophil elastase (NE), cathepsin G (CG), proteinase 3 (PR3) and neutrophil serine proteinase 4 (NSP4), are important in the pathogenesis of ALI/ARDS. Therefore, Serpins may protect lung tissue by inhibiting NSPs. However, the specific mechanism of Serpins is not totally clear. In this article, we will discuss the mechanism of action of NSPs in the inflammatory response of ALI/ARDS, the structural overview of Serpins, the primary role of Serpins in ALI/ARDS, such as the inhibition of NSPs activity, other roles of Serpins in ALI/ARDS, such as the inhibition of inflammatory factor release, regulation of apoptosis and protection of vascular endothelial cells and pulmonary surfactant-associated glycoprotein D (SP-D), and the clinical application of exogenous Serpins in ALI/ARDS to explore the role of Serpins in the pathogenesis of ALI/ARDS. The aim is to provide new ideas and strategies for the clinical treatment of ALI/ARDS.
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