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The mucus and mucins of the goblet cells and enterocytes provide the first defense line of the gastrointestinal tract and interact with the immune system

机译:杯状细胞和肠上皮细胞的粘液和粘蛋白提供了胃肠道的第一道防线,并与免疫系统相互作用

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The gastrointestinal tract is covered by mucus that has different properties in the stomach, small intestine, and colon. The large highly glycosylated gel-forming mucins MUC2 and MUC5AC are the major components of the mucus in the intestine and stomach, respectively. In the small intestine, mucus limits the number of bacteria that can reach the epithelium and the Peyer's patches. In the large intestine, the inner mucus layer separates the commensal bacteria from the host epithelium. The outer colonic mucus layer is the natural habitat for the commensal bacteria. The intestinal goblet cells secrete not only the MUC2 mucin but also a number of typical mucus components: CLCA1, FCGBP, AGR2, ZG16, and TFF3. The goblet cells have recently been shown to have a novel gate-keeping role for the presentation of oral antigens to the immune system. Goblet cells deliver small intestinal luminal material to the lamina propria dendritic cells of the tolerogenic CD103~+ type. In addition to the gel-forming mucins, the transmem-brane mucins MUC3, MUC12, and MUC17 form the enterocyte glyco-calyx that can reach about a micrometer out from the brush border. The MUC17 mucin can shuttle from a surface to an intracellular vesicle localization, suggesting that enterocytes might control and report epithelial microbial challenge. There is communication not only from the epithelial cells to the immune system but also in the opposite direction. One example of this is IL10 that can affect and improve the properties of the inner colonic mucus layer. The mucus and epithelial cells of the gastrointestinal tract are the primary gate keepers and controllers of bacterial interactions with the host immune system, but our understanding of this relationship is still in its infancy.
机译:胃肠道被粘液覆盖,在胃,小肠和结肠中具有不同的特性。高度高度糖基化的形成凝胶的粘蛋白MUC2和MUC5AC分别是肠和胃中粘液的主要成分。在小肠中,粘液限制了可以到达上皮和淋巴集结的细菌数量。在大肠中,内部粘液层将共生细菌与宿主上皮分开。结肠外粘液层是共生细菌的天然栖息地。肠杯状细胞不仅分泌MUC2粘蛋白,而且还分泌许多典型的粘液成分:CLCA1,FCGBP,AGR2,ZG16和TFF3。最近已经证明,杯状细胞对于将口服抗原呈递给免疫系统具有新的守门作用。杯状细胞将小肠腔内物质输送至致耐受性CD103〜+型固有层树突状细胞。除形成凝胶的粘蛋白外,跨膜粘蛋白MUC3,MUC12和MUC17形成肠上皮糖萼,可从刷缘伸出约一微米。 MUC17粘蛋白可以从表面穿梭到细胞内囊泡定位,表明肠上皮细胞可能控制并报告上皮微生物攻击。不仅从上皮细胞到免疫系统还有通讯,而且方向相反。 IL10就是一个例子,它可以影响并改善内结肠粘液层的特性。胃肠道的粘液和上皮细胞是细菌与宿主免疫系统相互作用的主要门控者和控制者,但我们对这种关系的了解仍处于起步阶段。

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