Neonatal microbiota colonization primes maturation of goblet cell-mediated protection in the pre-weaning colon.

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-08-04 Epub Date: 2025-05-05 DOI:10.1084/jem.20241591
Åsa Johansson, Mahadevan Venkita Subramani, Bahtiyar Yilmaz, Elisabeth E L Nyström, Elena Layunta, Liisa Arike, Felix Sommer, Philip Rosenstiel, Lars Vereecke, Louise Mannerås-Holm, Andy Wullaert, Thaher Pelaseyed, Malin E V Johansson, George M H Birchenough
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引用次数: 0

Abstract

Regulated host-microbe interactions are a critical aspect of lifelong health. Colonic goblet cells protect from microorganisms via the generation of a mucus barrier structure. Bacteria-sensing sentinel goblet cells provide secondary protection by orchestrating mucus secretion when microbes breach the mucus barrier. Mucus deficiencies in germ-free mice implicate a role for the microbiota in programming barrier generation, but its natural ontogeny remains undefined. We now investigate the mucus barrier and sentinel goblet cell development in relation to postnatal colonization. Combined in vivo and ex vivo analyses demonstrate rapid and sequential microbiota-dependent development of these primary and secondary goblet cell protective functions, with dynamic changes in mucus processing dependent on innate immune signaling via MyD88 and development of functional sentinel goblet cells dependent on the NADPH/dual oxidase family member Duox2. Our findings identify new mechanisms of microbiota-goblet cell regulatory interaction and highlight the critical importance of the pre-weaning period for the normal development of protective systems that are key legislators of host-microbiota interaction.

新生儿微生物群定植启动断奶前结肠杯状细胞介导的保护成熟。
调节宿主-微生物相互作用是终身健康的一个关键方面。结肠杯状细胞通过产生粘液屏障结构来保护微生物。当微生物突破粘液屏障时,细菌感应哨兵杯状细胞通过协调粘液分泌提供二级保护。无菌小鼠的粘液缺乏暗示了微生物群在编程屏障生成中的作用,但其自然成因仍不明确。我们现在研究黏液屏障和前哨杯状细胞的发育与产后定植的关系。结合体内和离体分析表明,这些初级和次级杯状细胞保护功能的快速和顺序依赖于微生物群的发展,粘液加工的动态变化依赖于先天免疫信号MyD88,以及依赖于NADPH/双氧化酶家族成员Duox2的功能性前哨杯状细胞的发展。我们的研究结果确定了微生物-杯状细胞调节相互作用的新机制,并强调了断奶前时期对宿主-微生物相互作用的关键立法者保护系统正常发育的关键重要性。
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
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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