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压力通过亚精胺介导的I型干扰素水平下降引发腹泻型肠易激综合征。

Stress triggers irritable bowel syndrome with diarrhea through a spermidine-mediated decline in type I interferon.

作者信息

Zhang Li, Wang Hao-Li, Zhang Ya-Fang, Mao Xin-Tao, Wu Ting-Ting, Huang Zhi-Hui, Jiang Wan-Jun, Fan Ke-Qi, Liu Dan-Dan, Yang Bing, Zhuang Mei-Hui, Huang Guang-Ming, Liang Yinming, Zhu Shu Jeffrey, Zhong Jiang-Yan, Xu Guang-Yin, Li Xiao-Ming, Cao Qian, Li Yi-Yuan, Jin Jin

机构信息

Center for Neuroimmunology and Health Longevity, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China; Department of Gastroenterology, Sir Run Run Shaw Hospital, College of Medicine Zhejiang University, Hangzhou 310016, China.

The MOE Key Laboratory of Biosystems Homeostasis & Protection, Zhejiang Provincial Key Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, Zhejiang 310058, China.

出版信息

Cell Metab. 2025 Jan 7;37(1):87-103.e10. doi: 10.1016/j.cmet.2024.09.002. Epub 2024 Oct 3.

DOI:10.1016/j.cmet.2024.09.002
PMID:39366386
Abstract

Irritable bowel syndrome with diarrhea (IBS-D) is a common and chronic gastrointestinal disorder that is characterized by abdominal discomfort and occasional diarrhea. The pathogenesis of IBS-D is thought to be related to a combination of factors, including psychological stress, abnormal muscle contractions, and inflammation and disorder of the gut microbiome. However, there is still a lack of comprehensive analysis of the logical regulatory correlation among these factors. In this study, we found that stress induced hyperproduction of xanthine and altered the abundance and metabolic characteristics of Lactobacillus murinus in the gut. Lactobacillus murinus-derived spermidine suppressed the basal expression of type I interferon (IFN)-α in plasmacytoid dendritic cells by inhibiting the K63-linked polyubiquitination of TRAF3. The reduction in IFN-α unrestricted the contractile function of colonic smooth muscle cells, resulting in an increase in bowel movement. Our findings provided a theoretical basis for the pathological mechanism of, and new drug targets for, stress-exposed IBS-D.

摘要

腹泻型肠易激综合征(IBS-D)是一种常见的慢性胃肠道疾病,其特征为腹部不适和偶尔腹泻。IBS-D的发病机制被认为与多种因素的组合有关,包括心理压力、异常肌肉收缩以及肠道微生物群的炎症和紊乱。然而,目前仍缺乏对这些因素之间逻辑调控相关性的全面分析。在本研究中,我们发现压力诱导黄嘌呤过量产生,并改变了肠道中鼠李糖乳杆菌的丰度和代谢特征。鼠李糖乳杆菌衍生的亚精胺通过抑制TRAF3的K63连接的多聚泛素化来抑制浆细胞样树突状细胞中I型干扰素(IFN)-α的基础表达。IFN-α的减少解除了结肠平滑肌细胞收缩功能的限制,导致肠道蠕动增加。我们的研究结果为应激暴露的IBS-D的病理机制和新的药物靶点提供了理论依据。

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