Intestinal interstitial fluid isolation provides novel insight into the human host-microbiome interface

IF 10.2 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Ellen G Avery, Lea-Maxie Haag, Victoria McParland, Sarah M Kedziora, Gabriel J Zigra, Daniela S Valdes, Marieluise Kirchner, Oliver Popp, Sabrina Geisberger, Olivia Nonn, Tine V Karlsen, Gabriele N’Diaye, Alex Yarritu, Hendrik Bartolomaeus, Theda U P Bartolomaeus, Nurana A Tagiyeva, Moritz I Wimmer, Nadine Haase, Yiming D Zhang, Andreas Wilhelm, Gerald Grütz, Olav Tenstad, Nicola Wilck, Sofia K Forslund, Robert Klopfleisch, Anja A Kühl, Raja Atreya, Stefan Kempa, Philipp Mertins, Britta Siegmund, Helge Wiig, Dominik N Müller
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引用次数: 0

Abstract

Aims The gastrointestinal (GI) tract is composed of distinct sub-regions, which exhibit segment-specific differences in microbial colonization and (patho)physiological characteristics. Gut microbes can be collectively considered as an active endocrine organ. Microbes produce metabolites, which can be taken up by the host and can actively communicate with the immune cells in the gut lamina propria with consequences for cardiovascular health. Variation in bacterial load and composition along the GI tract may influence the mucosal microenvironment and thus be reflected its interstitial fluid (IF). Characterization of the segment-specific microenvironment is challenging and largely unexplored because of lack of available tools. Methods and results Here, we developed methods, namely tissue centrifugation and elution, to collect IF from the mucosa of different intestinal segments. These methods were first validated in rats and mice, and the tissue elution method was subsequently translated for use in humans. These new methods allowed us to quantify microbiota-derived metabolites, mucosa-derived cytokines, and proteins at their site-of-action. Quantification of short-chain fatty acids showed enrichment in the colonic IF. Metabolite and cytokine analyses revealed differential abundances within segments, often significantly increased compared to plasma, and proteomics revealed that proteins annotated to the extracellular phase were site-specifically identifiable in IF. Lipopolysaccharide injections in rats showed significantly higher ileal IL-1β levels in IF compared to the systemic circulation, suggesting the potential of local as well as systemic effect. Conclusion Collection of IF from defined segments and the direct measurement of mediators at the site-of-action in rodents and humans bypasses the limitations of indirect analysis of faecal samples or serum, providing direct insight into this understudied compartment.
肠间质液分离为人类宿主-微生物界面提供了新的见解
胃肠道由不同的亚区组成,这些亚区在微生物定植和(病理)生理特征方面表现出不同的节段特异性差异。肠道微生物是一种活跃的内分泌器官。微生物产生代谢物,这些代谢物可以被宿主吸收,并可以主动与肠道固有层中的免疫细胞交流,从而对心血管健康产生影响。胃肠道细菌负荷和组成的变化可能影响粘膜微环境,从而反映其间质液(IF)。由于缺乏可用的工具,细分特定微环境的表征具有挑战性,并且在很大程度上未被探索。方法与结果本研究采用组织离心和洗脱法收集不同肠段黏膜的IF。这些方法首先在大鼠和小鼠中得到验证,组织洗脱法随后被翻译用于人类。这些新方法使我们能够定量微生物衍生的代谢物,粘膜衍生的细胞因子和作用位点的蛋白质。短链脂肪酸定量显示结肠IF富集。代谢物和细胞因子分析显示,与血浆相比,片段内的丰度差异通常显著增加,蛋白质组学显示,在IF中注释到细胞外期的蛋白质是位点特异性可识别的。与体循环相比,大鼠注射脂多糖可显著提高IF中回肠IL-1β水平,提示其可能具有局部和全身作用。从确定的片段中收集干扰素,并在啮齿动物和人类的作用部位直接测量介质,绕过了粪便样本或血清间接分析的局限性,可以直接了解这一未被研究的区域。
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
Cardiovascular Research
Cardiovascular Research 医学-心血管系统
CiteScore
21.50
自引率
3.70%
发文量
547
审稿时长
1 months
期刊介绍: Cardiovascular Research Journal Overview: International journal of the European Society of Cardiology Focuses on basic and translational research in cardiology and cardiovascular biology Aims to enhance insight into cardiovascular disease mechanisms and innovation prospects Submission Criteria: Welcomes papers covering molecular, sub-cellular, cellular, organ, and organism levels Accepts clinical proof-of-concept and translational studies Manuscripts expected to provide significant contribution to cardiovascular biology and diseases
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