MAIT 细胞:墙壁上的守望者

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-01-06 Epub Date: 2024-10-24 DOI:10.1084/jem.20232298
Lilou Germain, Pablo Veloso, Olivier Lantz, François Legoux
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引用次数: 0

摘要

MAIT 细胞是驻留在肺部、皮肤和肠道等屏障组织中的先天性类 T 细胞。MAIT细胞的半变异T细胞受体和限制元件MR1在哺乳动物中都是高度保守的,表明其功能与抗原特异性无关。不同物种的 MAIT 细胞同时表达细胞毒性基因和组织修复基因,表明其具有多功能性。因此,MAIT 细胞有助于抗菌反应和修复受损的屏障组织。MAIT 细胞能识别核黄素生物合成途径衍生的代谢物,这些代谢物能迅速穿过上皮屏障,由抗原递呈细胞递呈。肠道炎症期间肠道生态的变化推动了核黄素和 MAIT 配体生产者的扩张。因此,MAIT 细胞可以在完整的上皮细胞内实时监测微生物群失调情况,并提供快速且与环境相关的反应。在此,我们将讨论有关 MAIT 配体的起源和调控以及 MAIT 细胞在屏障组织中的作用的最新发现。我们推测了 MAIT 细胞在进化过程中保持不变的潜在原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MAIT cells: Conserved watchers on the wall.

MAIT cells are innate-like T cells residing in barrier tissues such as the lung, skin, and intestine. Both the semi-invariant T cell receptor of MAIT cells and the restricting element MR1 are deeply conserved across mammals, indicating non-redundant functions linked to antigenic specificity. MAIT cells across species concomitantly express cytotoxicity and tissue-repair genes, suggesting versatile functions. Accordingly, MAIT cells contribute to antibacterial responses as well as to the repair of damaged barrier tissues. MAIT cells recognize riboflavin biosynthetic pathway-derived metabolites, which rapidly cross epithelial barriers to be presented by antigen-presenting cells. Changes in gut ecology during intestinal inflammation drive the expansion of strong riboflavin and MAIT ligand producers. Thus, MAIT cells may enable real-time surveillance of microbiota dysbiosis across intact epithelia and provide rapid and context-dependent responses. Here, we discuss recent findings regarding the origin and regulation of MAIT ligands and the role of MAIT cells in barrier tissues. We speculate on the potential reasons for MAIT cell conservation during evolution.

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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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