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牛奶磷脂通过 Notch 通路改善与结肠杯状细胞耗竭相关的小鼠结肠炎。

Milk phospholipids ameliorate mouse colitis associated with colonic goblet cell depletion via the Notch pathway.

机构信息

School of Food Science and Biotechnology, Zhejiang Gongshang University, Hangzhou 310018, China.

出版信息

Food Funct. 2019 Aug 1;10(8):4608-4619. doi: 10.1039/c9fo00690g. Epub 2019 Jul 10.

DOI:10.1039/c9fo00690g
PMID:31290530
Abstract

As natural emulsifiers used in food products, phospholipids have been gaining increasing attention, whereas their intestinal health impacts are still unclear. This work aims to investigate the effect of milk phospholipids (MP) on dextran sodium sulfate (DSS)-induced colitis of C57BL/6 mice, compared with soybean phospholipids (SP), as well as the related mechanism. We found that unlike SP, MP supplementation (25 mg per kg BW) had a unique beneficial effect on the 2.5% DSS induced colitis (p < 0.05) and ameliorated the injury status of goblet cells, indicated by the increased number (p < 0.05) and size (p < 0.05) of the goblet cells and more acid mucins and antimicrobial peptides (p < 0.05). Meanwhile, MP supplementation restored the over-activated Notch pathway through balancing the level of Notch pathway ligand Dll4 in the colon subepithelial layer (p < 0.05), thus leading to the increase in the Math1 expression (p < 0.05), and consequently enhanced goblet cell restitution (p < 0.05). Furthermore, MP induced more goblet cells in the colonoid and colonic myofibroblast co-culture system (p < 0.05), which highlighted the indispensable role of colonic myofibroblasts, as an intestinal stem cell niche factor, in the goblet cell modulation effect of MP. These findings indicated that phospholipids from milk instead of soybean attenuated the severity of DSS-induced mouse colitis and prevented the depletion of colonic goblet cells through balancing the over-activated Notch pathway mediated by colonic myofibroblasts.

摘要

作为食品中常用的天然乳化剂,磷脂越来越受到关注,但它们对肠道健康的影响尚不清楚。本研究旨在对比大豆磷脂(SP),研究乳磷脂(MP)对葡聚糖硫酸钠(DSS)诱导的 C57BL/6 小鼠结肠炎的影响及其相关机制。结果发现,与 SP 不同,MP 补充剂(25mg/kgBW)对 2.5%DSS 诱导的结肠炎具有独特的有益作用(p<0.05),并改善了杯状细胞的损伤状态,表现为杯状细胞数量增加(p<0.05)和体积增大(p<0.05),以及酸性粘蛋白和抗菌肽增多(p<0.05)。同时,MP 补充剂通过平衡结肠黏膜下层 Notch 通路配体 Dll4 的水平(p<0.05),恢复了过度激活的 Notch 通路,从而导致 Math1 表达增加(p<0.05),进而增强了杯状细胞修复(p<0.05)。此外,MP 在类器官和结肠肌成纤维细胞共培养系统中诱导更多的杯状细胞(p<0.05),这突出了结肠肌成纤维细胞作为肠干细胞龛因子在 MP 调节杯状细胞中的不可或缺作用。这些发现表明,与大豆磷脂相比,乳磷脂可减轻 DSS 诱导的小鼠结肠炎的严重程度,并通过平衡结肠肌成纤维细胞介导的过度激活的 Notch 通路来防止结肠杯状细胞的耗竭。

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