微生物代谢产物对先天淋巴样细胞的调控。

IF 4.8 3区 医学 Q1 GENETICS & HEREDITY
Journal of Molecular Medicine-Jmm Pub Date : 2025-05-01 Epub Date: 2025-03-25 DOI:10.1007/s00109-025-02530-3
Hongji Tao, Jingjing Geng, Long Bai, Dan Su, Yu Zhao, Guifang Xu, Mingming Zhang
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引用次数: 0

摘要

先天淋巴样细胞(ILCs)是一类独特的免疫细胞,缺乏抗原特异性受体,但具有检测周围组织信号的能力。大多数ilc存在于淋巴组织和粘膜组织中,与微生物群保持密切联系。除了辅助细胞和适应性免疫细胞的作用外,越来越多的研究表明,微生物代谢物在介导ILCs与微生物群之间的关系中起着至关重要的作用。在这篇综述中,我们强调并总结了来自不同来源的微生物代谢物在调节ILC亚群中的作用,并提出这些代谢物可能是ILC介导疾病的潜在治疗机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of innate lymphoid cell by microbial metabolites.

Innate lymphoid cells (ILCs) are a unique category of immune cell that lack antigen-specific receptors yet possess the capacity to detect signals from the surrounding tissue. The majority of ILCs reside in the lymphoid and mucosal tissues, maintaining close associations with the microbiota. Beyond the contributions of accessory cells and adaptive immune cells, accumulating studies demonstrate that microbial metabolites serve a crucial role in mediating the relationship between ILCs and the microbiota. In this review, we highlight and summarize the roles of microbial metabolites from different sources in modulating ILC subsets, proposing these metabolites as potential therapeutic mechanisms in ILC-mediated diseases.

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来源期刊
Journal of Molecular Medicine-Jmm
Journal of Molecular Medicine-Jmm 医学-医学:研究与实验
CiteScore
9.30
自引率
0.00%
发文量
100
审稿时长
1.3 months
期刊介绍: The Journal of Molecular Medicine publishes original research articles and review articles that range from basic findings in mechanisms of disease pathogenesis to therapy. The focus includes all human diseases, including but not limited to: Aging, angiogenesis, autoimmune diseases as well as other inflammatory diseases, cancer, cardiovascular diseases, development and differentiation, endocrinology, gastrointestinal diseases and hepatology, genetics and epigenetics, hematology, hypoxia research, immunology, infectious diseases, metabolic disorders, neuroscience of diseases, -omics based disease research, regenerative medicine, and stem cell research. Studies solely based on cell lines will not be considered. Studies that are based on model organisms will be considered as long as they are directly relevant to human disease.
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