Mesenchymal stem cells alleviate sepsis-induced acute lung injury by blocking neutrophil extracellular traps formation and inhibiting ferroptosis in rats

• Published in: PeerJ (San Francisco, CA) CA), 2024, Vol.12, p.e16748-e16748, Article e16748
• Main Authors: Wang, TieNan, Zhang, Zheng, Deng, Zhizhao, Zeng, Weiqi, Gao, Yingxin, Hei, Ziqing, Yuan, Dongdong
• Format: Article
• Language: English
• Subjects: Acute lung injury; Bone marrow; Cecum; Cell Biology; Deoxyribonuclease; Experiments; Ferroptosis; Histology; Laboratory animals; Leukocytes (neutrophilic); Lungs; Mesenchymal stem cells; Molecular Biology; Morbidity; Neutrophil extracellular traps; Neutrophils; Pathology; Respiratory Medicine; Sepsis; Signal transduction; Stem cells; Therapeutic targets
• ISSN: 2167-8359; 2167-8359
• DOI: 10.7717/peerj.16748

Acute lung injury (ALI) is one of the most serious complications of sepsis, characterized by high morbidity and mortality rates. Ferroptosis has recently been reported to play an essential role in sepsis-induced ALI. Excessive neutrophil extracellular traps (NETs) formation induces exacerbated inflammation and is crucial to the development of ALI. In this study, we explored the effects of ferroptosis and NETs and observed the therapeutic function of mesenchymal stem cells (MSCs) on sepsis-induced ALI. First, we produced a cecal ligation and puncture (CLP) model of sepsis in rats. Ferrostain-1 and DNase-1 were used to inhibit ferroptosis and NETs formation separately, to confirm their effects on sepsis-induced ALI. Next, U0126 was applied to suppress the MEK/ERK signaling pathway, which is considered to be vital to NETs formation. Finally, the therapeutic effect of MSCs was observed on CLP models. The results demonstrated that both ferrostain-1 and DNase-1 application could improve sepsis-induced ALI. DNase-1 inhibited ferroptosis significantly in lung tissues, showing that ferroptosis could be regulated by NETs formation. With the inhibition of the MEK/ERK signaling pathway by U0126, NETs formation and ferroptosis in lung tissues were both reduced, and sepsis-induced ALI was improved. MSCs also had a similar protective effect against sepsis-induced ALI, not only inhibiting MEK/ERK signaling pathway-mediated NETs formation, but also alleviating ferroptosis in lung tissues. We concluded that MSCs could protect against sepsis-induced ALI by suppressing NETs formation and ferroptosis in lung tissues. In this study, we found that NETs formation and ferroptosis were both potential therapeutic targets for the treatment of sepsis-induced ALI, and provided new evidence supporting the clinical application of MSCs in sepsis-induced ALI treatment.