Liu Li, Zheng Cihua, Xu Zhenyang, Wang Zhuoya, Zhong Yuchun, He Zhidong, Zhang Wenming, Zhang Yuanbing
Clinical School of Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, China.
The Institute of Translational Medicine, The Second Affiliated Hospital of Nanchang University, Nanchang University, Nanchang, Jiangxi, China.
Microbiol Spectr. 2024 Oct 29;12(12):e0210824. doi: 10.1128/spectrum.02108-24.
Acute lung injury (ALI) is associated with high morbidity and mortality rates. However, its clinical treatment is limited. Currently, the treatment of lung diseases by regulating the lung microbiota has become a research hotspot. In this study, we investigated the protective effects of the intranasal administration of and its derived extracellular vesicles (EVs) against lipopolysaccharide (LPS)-induced ALI. The results demonstrated that compared with the LPS group, the pre-treatment group with and its EVs reduced the expression of pro-inflammatory cytokines and alleviated the symptoms in ALI mice by inhibiting the TLR4/MyD88 signaling pathway. Moreover, and its derived EVs inhibited the expression of apoptosis-related proteins and increased the expression of lung barrier proteins. Additionally, the intervention of changed the composition of the pulmonary microbiota. At the species level, LPS significantly increased the relative abundance of , while reversed this effect. In conclusion, these data demonstrate that intranasal administration of and its EVs can prevent LPS-induced ALI by reducing inflammation, inhibiting apoptosis, and improving lung barrier function. Additionally, regulated the pulmonary microbiota of mice to alleviate LPS-induced ALI.IMPORTANCEThe disorder of pulmonary microbiota plays an important role in the progression of acute lung injury (ALI). However, very few studies have been conducted to treat ALI by modulating pulmonary microbiota. In this study, the diversity and composition of pulmonary microbiota were altered in lipopolysaccharide (LPS)-induced ALI mice, but the ecological balance of the pulmonary microbiota was restored by intranasal administration of . Moreover, the study reported the mechanism of and its derived extracellular vesicles for the treatment of LPS-induced ALI. These results reveal the importance of pulmonary microbiota in ALI disease. It provides a new approach for the treatment of ALI with new-generation probiotics.
急性肺损伤(ALI)的发病率和死亡率都很高。然而,其临床治疗手段有限。目前,通过调节肺部微生物群来治疗肺部疾病已成为一个研究热点。在本研究中,我们调查了经鼻给予[具体物质]及其衍生的细胞外囊泡(EVs)对脂多糖(LPS)诱导的ALI的保护作用。结果表明,与LPS组相比,用[具体物质]及其EVs预处理的组通过抑制TLR4/MyD88信号通路降低了促炎细胞因子的表达,并减轻了ALI小鼠的症状。此外,[具体物质]及其衍生的EVs抑制了凋亡相关蛋白的表达,并增加了肺屏障蛋白的表达。此外,[具体物质]的干预改变了肺部微生物群的组成。在物种水平上,LPS显著增加了[某种微生物]的相对丰度,而[具体物质]则逆转了这种效应。总之,这些数据表明,经鼻给予[具体物质]及其EVs可以通过减轻炎症、抑制凋亡和改善肺屏障功能来预防LPS诱导的ALI。此外,[具体物质]调节了小鼠的肺部微生物群以减轻LPS诱导的ALI。
重要性
肺部微生物群紊乱在急性肺损伤(ALI)的进展中起重要作用。然而,通过调节肺部微生物群来治疗ALI的研究很少。在本研究中,脂多糖(LPS)诱导的ALI小鼠的肺部微生物群的多样性和组成发生了改变,但经鼻给予[具体物质]可恢复肺部微生物群的生态平衡。此外,该研究报道了[具体物质]及其衍生的细胞外囊泡治疗LPS诱导的ALI的机制。这些结果揭示了肺部微生物群在ALI疾病中的重要性。它为用新一代益生菌治疗ALI提供了一种新方法。