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核因子红细胞 2 相关因子 2 干预脂多糖诱导的急性肺损伤小鼠中性粒细胞胞外诱捕网的释放。

Nuclear Factor Erythroid 2-Related Factor 2 Intervenes the Release of Neutrophil Extracellular Traps during Lipopolysaccharide-Induced Acute Lung Injury in Mice.

机构信息

Department of Critical Care Medicine The First Hospital of Jilin University, Changchun, Jilin 130021, China.

Department of Critical Care Medicine Huazhong University of Science and Technology Union Shenzhen Hospital, Shenzhen, Guangdong 518000, China.

出版信息

Mediators Inflamm. 2024 Aug 29;2024:8847492. doi: 10.1155/2024/8847492. eCollection 2024.

DOI:10.1155/2024/8847492
PMID:39238946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11377114/
Abstract

The pathogenesis of acute lung injury is complex. Studies have demonstrated the role of neutrophil extracellular traps (NETs) in the process of lipopolysaccharide (LPS)-induced acute lung injury (ALI). However, the underlying mechanism remains unclear. In this study, the regulation of Nrf2 in the formation of NETs, which was pathogenic in LPS-induced ALI, was identified by analyzing the levels of Cit-H3, lung function, lung tissue pathology, lung wet/dry ratio, the inflammatory cells, cytokines and proteins in the bronchoalveolar lavage fluid (BALF) and in addition, the activity of lung myeloperoxidase (MPO) was also measured. Results showed that the levels of Cit-H3 measured by western blot in Nrf2-knockout (KO) mice were higher compared with the WT mice after LPS stimulation. To further investigate the NETs formation was pathogenic during LPS-induced ALI, the Nrf2-KO mice were treated with DNase I. Results showed that DNase I improved lung function and lung tissue pathology and significantly reduced lung wet/dry ratio and proteins in the BALF. Besides, DNase I also attenuated the infiltration of inflammatory cells and the cytokines (TNF-, IL-1) production in the BALF and the activity of lung MPO. Therefore, these results together indicate that Nrf2 may intervene in the release of NETs during LPS-induced ALI in mice.

摘要

急性肺损伤的发病机制较为复杂。有研究表明中性粒细胞胞外诱捕网(NETs)在脂多糖(LPS)诱导的急性肺损伤(ALI)过程中发挥作用。然而,其潜在机制尚不清楚。本研究通过分析组蛋白 H3 三甲基化(Cit-H3)水平、肺功能、肺组织病理学、肺湿/干重比、支气管肺泡灌洗液(BALF)中的炎症细胞、细胞因子和蛋白质,以及肺髓过氧化物酶(MPO)活性,鉴定了 Nrf2 在 LPS 诱导的 ALI 中致病性 NETs 形成中的调节作用。结果表明,LPS 刺激后 Nrf2 敲除(KO)小鼠的 western blot 检测到的 Cit-H3 水平高于野生型(WT)小鼠。为了进一步研究 NETs 形成在 LPS 诱导的 ALI 中的致病性,用 DNase I 处理 Nrf2-KO 小鼠。结果表明,DNase I 改善了肺功能和肺组织病理学,显著降低了肺湿/干重比和 BALF 中的蛋白质水平。此外,DNase I 还减轻了 BALF 中炎症细胞的浸润和细胞因子(TNF-α、IL-1)的产生以及肺 MPO 的活性。因此,这些结果共同表明,Nrf2 可能参与了 LPS 诱导的 ALI 中 NETs 的释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/f17b97381980/MI2024-8847492.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/6ea839264f81/MI2024-8847492.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/dac6c936fd9b/MI2024-8847492.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/2725aad79869/MI2024-8847492.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/f17b97381980/MI2024-8847492.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/6ea839264f81/MI2024-8847492.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/dac6c936fd9b/MI2024-8847492.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/2725aad79869/MI2024-8847492.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d03/11377114/f17b97381980/MI2024-8847492.004.jpg

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