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人乳寡糖对成人肠道菌群和屏障功能的影响。

Effects of Human Milk Oligosaccharides on the Adult Gut Microbiota and Barrier Function.

机构信息

Quadram Institute Bioscience, Gut Microbes and Health Institute Strategic Programme, Norwich Research Park, Norwich NR4 7UQ, UK.

Glycom A/S, Kogle Allé 4, DK-2970 Hørsholm, Denmark.

出版信息

Nutrients. 2020 Sep 13;12(9):2808. doi: 10.3390/nu12092808.

Abstract

Human milk oligosaccharides (HMOs) shape the gut microbiota in infants by selectively stimulating the growth of bifidobacteria. Here, we investigated the impact of HMOs on adult gut microbiota and gut barrier function using the Simulator of the Human Intestinal Microbial Ecosystem (SHIME), Caco2 cell lines, and human intestinal gut organoid-on-chips. We showed that fermentation of 2'-O-fucosyllactose (2'FL), lacto-N-neotetraose (LNnT), and combinations thereof (MIX) led to an increase of bifidobacteria, accompanied by an increase of short chain fatty acid (SCFA), in particular butyrate with 2'FL. A significant reduction in paracellular permeability of FITC-dextran probe was observed using Caco2 cell monolayers with fermented 2'FL and MIX, which was accompanied by an increase in claudin-8 gene expression as shown by qPCR, and a reduction in IL-6 as determined by multiplex ELISA. Using gut-on-chips generated from human organoids derived from proximal, transverse, and distal colon biopsies (Colon Intestine Chips), we showed that claudin-5 was significantly upregulated across all three gut-on-chips following treatment with fermented 2'FL under microfluidic conditions. Taken together, these data show that, in addition to their bifidogenic activity, HMOs have the capacity to modulate immune function and the gut barrier, supporting the potential of HMOs to provide health benefits in adults.

摘要

人乳寡糖 (HMOs) 通过选择性地刺激双歧杆菌的生长来塑造婴儿肠道微生物群。在这里,我们使用人类肠道微生物生态系统模拟器 (SHIME)、Caco2 细胞系和人类肠道类器官芯片研究了 HMOs 对成人肠道微生物群和肠道屏障功能的影响。我们表明,2'-岩藻糖基乳糖 (2'FL)、乳-N-新四糖 (LNnT) 及其组合 (MIX) 的发酵导致双歧杆菌增加,伴随着短链脂肪酸 (SCFA) 的增加,特别是 2'FL 的丁酸。用发酵的 2'FL 和 MIX 处理 Caco2 细胞单层时,FITC-葡聚糖探针的细胞旁通透性显著降低,这伴随着 qPCR 显示的 Claudin-8 基因表达增加,以及通过多重 ELISA 确定的 IL-6 减少。使用源自近端、横结肠和远端结肠活检的人类类器官生成的肠道类器官芯片 (Colon Intestine Chips),我们表明,在微流体条件下用发酵的 2'FL 处理后,Claudin-5 在所有三个肠道类器官芯片中均显著上调。综上所述,这些数据表明,除了具有双歧杆菌活性外,HMOs 还具有调节免疫功能和肠道屏障的能力,这支持了 HMOs 在成人中提供健康益处的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d378/7551690/102bf8a59ab4/nutrients-12-02808-g001.jpg

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