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解析特定饮食和肠道微生物对炎症性肠病的影响。

Unravelling specific diet and gut microbial contributions to inflammatory bowel disease.

作者信息

Pereira Gabriel Vasconcelos, Boudaud Marie, Wolter Mathis, Alexander Celeste, De Sciscio Alessandro, Grant Erica T, Trindade Bruno Caetano, Pudlo Nicholas A, Singh Shaleni, Campbell Austin, Shan Mengrou, Zhang Li, Willieme Stéphanie, Kim Kwi, Denike-Duval Trisha, Bleich André, Schmidt Thomas M, Kennedy Lucy, Lyssiotis Costas A, Chen Grace Y, Eaton Kathryn A, Desai Mahesh S, Martens Eric C

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.

Department of Infection and Immunity, Luxembourg Institute of Health, 4354 Esch-sur-Alzette, Luxembourg.

出版信息

Res Sq. 2023 Mar 13:rs.3.rs-2518251. doi: 10.21203/rs.3.rs-2518251/v1.

Abstract

Inflammatory bowel disease (IBD) is a chronic condition characterized by periods of spontaneous intestinal inflammation and is increasing in industrialized populations. Combined with host genetic predisposition, diet and gut bacteria are thought to be prominent features contributing to IBD, but little is known about the precise mechanisms involved. Here, we show that low dietary fiber promotes bacterial erosion of protective colonic mucus, leading to lethal colitis in mice lacking the IBD-associated cytokine, interleukin-10. Diet-induced inflammation is driven by mucin-degrading bacteria-mediated Th1 immune responses and is preceded by expansion of natural killer T cells and reduced immunoglobulin A coating of some bacteria. Surprisingly, an exclusive enteral nutrition diet, also lacking dietary fiber, reduced disease by increasing bacterial production of isobutyrate, which is dependent on the presence of a specific bacterial species, . Our results illuminate a mechanistic framework using gnotobiotic mice to unravel the complex web of diet, host and microbial factors that influence IBD.

摘要

炎症性肠病(IBD)是一种慢性疾病,其特征为肠道会自发出现炎症,且在工业化人群中的发病率呈上升趋势。饮食和肠道细菌与宿主遗传易感性共同作用,被认为是导致IBD的主要因素,但其中具体机制仍知之甚少。在此,我们发现低膳食纤维会促使结肠保护性黏液受到细菌侵蚀,从而导致缺乏IBD相关细胞因子白细胞介素-10的小鼠发生致命性结肠炎。饮食诱导的炎症由黏蛋白降解细菌介导的Th1免疫反应驱动,在此之前自然杀伤T细胞会扩增,且部分细菌的免疫球蛋白A包被会减少。令人惊讶的是,同样缺乏膳食纤维的全肠内营养饮食通过增加异丁酸的细菌生成量来减轻疾病,而异丁酸的产生依赖于一种特定细菌物种的存在。我们的研究结果利用无菌小鼠阐明了一个机制框架,以揭示影响IBD的饮食、宿主和微生物因素的复杂网络。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d5c/10055531/f73f5a681013/nihpp-rs2518251v1-f0007.jpg

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