中性粒细胞胞外陷阱
拟杆菌
肠道菌群
胰腺炎
失调
炎症
细胞外
急性胰腺炎
生物
免疫学
微生物群
全身炎症
牛磺酸
微生物学
医学
内科学
细胞生物学
细菌
生物信息学
生物化学
遗传学
氨基酸
作者
Guanqun Li,Liwei Liu,Tianqi Lu,Yuhang Sui,Can Zhang,Yongwei Wang,Tao Zhang,Yu Xie,Peng Xiao,Zhongjie Zhao,Chundong Cheng,Jisheng Hu,Hongze Chen,Dongbo Xue,Hua Chen,Gang Wang,Rui Kong,Hongtao Tan,Xuewei Bai,Zhibo Li
标识
DOI:10.1038/s41467-023-41950-y
摘要
Hypertriglyceridemic pancreatitis (HTGP) is featured by higher incidence of complications and poor clinical outcomes. Gut microbiota dysbiosis is associated with pancreatic injury in HTGP and the mechanism remains unclear. Here, we observe lower diversity of gut microbiota and absence of beneficial bacteria in HTGP patients. In a fecal microbiota transplantation mouse model, the colonization of gut microbiota from HTGP patients recruits neutrophils and increases neutrophil extracellular traps (NETs) formation that exacerbates pancreatic injury and systemic inflammation. We find that decreased abundance of Bacteroides uniformis in gut microbiota impairs taurine production and increases IL-17 release in colon that triggers NETs formation. Moreover, Bacteroides uniformis or taurine inhibits the activation of NF-κB and IL-17 signaling pathways in neutrophils which harness NETs and alleviate pancreatic injury. Our findings establish roles of endogenous Bacteroides uniformis-derived metabolic and inflammatory products on suppressing NETs release, which provides potential insights of ameliorating HTGP through gut microbiota modulation.
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