Neutrophil extracellular traps trigger alveolar epithelial cell necroptosis through the cGAS-STING pathway during acute lung injury in mice

• Published in: International journal of biological sciences Vol. 20; no. 12; pp. 4713 - 4730
• Main Authors: Sha, Han-Xi, Liu, Yu-Biao, Qiu, Yan-Ling, Zhong, Wen-Jing, Yang, Nan-Shi-Yu, Zhang, Chen-Yu, Duan, Jia-Xi, Xiong, Jian-Bing, Guan, Cha-Xiang, Zhou, Yong
• Format: Journal Article
• Language: English
• Published: Australia Ivyspring International Publisher 01.01.2024
• Subjects: Acute Lung Injury - metabolism; Acute Lung Injury - pathology; Alveolar Epithelial Cells - metabolism; Animals; Extracellular Traps - metabolism; Male; Membrane Proteins - metabolism; Mice; Mice, Inbred C57BL; Necroptosis; Neutrophils - metabolism; Nucleotidyltransferases - metabolism; Receptor-Interacting Protein Serine-Threonine Kinases - metabolism; Research Paper; Signal Transduction; Acute lung injury; Endocytosis; cGAS-STING; Necroptosis; Neutrophil extracellular traps; Alveolar epithelial cells
• ISSN: 1449-2288; 1449-2288
• DOI: 10.7150/ijbs.99456

Extensive loss of alveolar epithelial cells (AECs) undergoing necroptosis is a crucial mechanism of acute lung injury (ALI), but its triggering mechanism needs to be thoroughly investigated. Neutrophil extracellular traps (NETs) play a significant role in ALI. However, the effect of NETs on AECs' death has not been clarified. Our study found that intratracheal instillation of NETs disrupted lung tissue structure, suggesting that NETs could induce ALI in mice. Moreover, we observed that NETs could trigger necroptosis of AECs and . The phosphorylation levels of RIPK3 and MLKL were increased in MLE12 cells after NETs treatment ( < 0.05). Mechanistically, NETs taken up by AECs through endocytosis activated the cGAS-STING pathway and triggered AECs necroptosis. The expression of cGAS, STING, TBK1 and IRF3 were increased in MLE12 cells treated with NETs ( < 0.05). Furthermore, the cGAS inhibitor RU.521 inhibited NETs-triggered AECs necroptosis and alleviated the pulmonary damage induced by NETs in mice. In conclusion, our study demonstrates that NETs taken up by AECs endocytosis can activate the cGAS-STING pathway and trigger AECs necroptosis to promote ALI in mice. Our findings indicate that targeting the NETs/cGAS-STING/necroptosis pathway in AECs is an effective strategy for treating ALI.