Fecal Microbiota Transplantation Modulates Th17/Treg Balance via JAK/STAT Pathway in ARDS Rats.

IF 2.6 3区 生物学 Q3 MATERIALS SCIENCE, BIOMATERIALS
Dongwei Zhang, Biying Dong, Jie Chen, Zhenqiang Zhang, Weitong Zeng, Longxiong Liao, Xia Xiong, Xuejun Qin, Xianming Fan
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Abstract

This study evaluated the therapeutic effects of fecal microbiota transplantation (FMT) on lipopolysaccharide (LPS)-induced acute respiratory distress syndrome (ARDS) in rats. The study focused on the balance of T-helper 17 (Th17) and regulatory T (Treg) cells, as well as the modulation of the JAK/STAT pathway. This study established a rat ARDS model using intranasal LPS instillation, administering interventions such as FMT, Treg cell depletion, and JAK inhibitors. Assessments included histopathological examination of lung and intestinal tissues, flow cytometry for Th17 and Treg cell proportions, qPCR and Western blot for gene and protein expression, ELISA for inflammatory cytokines, and correlation analysis using Spearman's method for cytokine-immune cell interactions. Results indicated that FMT and JAK inhibitors significantly reduce lung damage induced by LPS, reduced alveolar destruction and inflammation, restored Th17/Treg balance, and inhibited JAK/STAT pathway activity. Notably, FMT decreased pro-inflammatory cytokines (IL-2, IL-6, IL-8, IL-17A, IL-23, TGF-β1) and increased anti-inflammatory cytokines (IL-10, IL-35) in serum. Spearman correlation analysis indicated that FMT restored immune balance by modulating the interactions between cytokines and immune cells. In conclusion, FMT effectively alleviates lung and intestinal injury in LPS-induced ARDS rat models by modulating Th17/Treg balance and inhibiting JAK/STAT pathway activity, demonstrating promising therapeutic potential for ARDS treatment.

粪便菌群移植通过JAK/STAT通路调节ARDS大鼠Th17/Treg平衡
本研究评价了粪便微生物群移植(FMT)对脂多糖(LPS)诱导的大鼠急性呼吸窘迫综合征(ARDS)的治疗作用。本研究主要关注辅助性T- 17 (Th17)和调节性T (Treg)细胞的平衡,以及JAK/STAT通路的调节。本研究采用鼻内注射LPS,给予FMT、Treg细胞耗尽和JAK抑制剂等干预措施,建立了大鼠ARDS模型。评估包括肺和肠组织病理学检查,流式细胞术检测Th17和Treg细胞比例,qPCR和Western blot检测基因和蛋白表达,ELISA检测炎症因子,使用Spearman方法进行细胞因子-免疫细胞相互作用的相关性分析。结果表明,FMT和JAK抑制剂可显著减轻LPS诱导的肺损伤,减轻肺泡破坏和炎症,恢复Th17/Treg平衡,抑制JAK/STAT通路活性。值得注意的是,FMT降低了血清中促炎因子(IL-2、IL-6、IL-8、IL-17A、IL-23、TGF-β1),升高了血清中抗炎因子(IL-10、IL-35)。Spearman相关分析表明,FMT通过调节细胞因子与免疫细胞之间的相互作用来恢复免疫平衡。综上所述,FMT通过调节Th17/Treg平衡和抑制JAK/STAT通路活性,有效缓解lps诱导的ARDS大鼠模型的肺和肠道损伤,显示出良好的ARDS治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced biology
Advanced biology Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
6.60
自引率
0.00%
发文量
130
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