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Akkermansia muciniphila Adheres to Enterocytes and Strengthens the Integrity of the Epithelial Cell Layer

机译:Akkermansia muciniphila坚持肠上皮细胞并增强上皮细胞层的完整性

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Akkermansia muciniphila is a Gram-negative mucin-degrading bacterium that resides in the gastrointestinal tracts of humans and animals. A. muciniphila has been linked with intestinal health and improved metabolic status in obese and type 2 diabetic subjects. Specifically, A. muciniphila has been shown to reduce high-fat-diet-induced endotoxemia, which develops as a result of an impaired gut barrier. Despite the accumulating evidence of the health-promoting effects of A. muciniphila , the mechanisms of interaction of the bacterium with the host have received little attention. In this study, we used several in vitro models to investigate the adhesion of A. muciniphila to the intestinal epithelium and its interaction with the host mucosa. We found that A. muciniphila adheres strongly to the Caco-2 and HT-29 human colonic cell lines but not to human colonic mucus. In addition, A. muciniphila showed binding to the extracellular matrix protein laminin but not to collagen I or IV, fibronectin, or fetuin. Importantly, A. muciniphila improved enterocyte monolayer integrity, as shown by a significant increase in the transepithelial electrical resistance (TER) of cocultures of Caco-2 cells with the bacterium. Further, A. muciniphila induced interleukin 8 (IL-8) production by enterocytes at cell concentrations 100-fold higher than those for Escherichia coli , suggesting a very low level of proinflammatory activity in the epithelium. In conclusion, our results demonstrate that A. muciniphila adheres to the intestinal epithelium and strengthens enterocyte monolayer integrity in vitro , suggesting an ability to fortify an impaired gut barrier. These results support earlier associative in vivo studies and provide insights into the interaction of A. muciniphila with the host.
机译:Akkermansia muciniphila是一种革兰氏阴性黏蛋白降解细菌,位于人类和动物的胃肠道中。黏液曲霉菌与肥胖和2型糖尿病患者的肠道健康和改善的代谢状况有关。具体而言,已显示出粘液曲霉可减少高脂饮食诱导的内毒素血症,这是由于肠屏障受损而导致的。尽管有累积的证据证明黏液曲霉对健康有促进作用,但细菌与宿主之间的相互作用机制却很少受到关注。在这项研究中,我们使用了几种体外模型来研究黏液曲霉对肠上皮的粘附及其与宿主黏膜的相互作用。我们发现黏液曲霉对Caco-2和HT-29人结肠细胞系具有很强的粘附力,但对人结肠粘液却没有。另外,黏液曲霉显示出与细胞外基质蛋白层粘连蛋白的结合,但不与胶原蛋白I或IV,纤连蛋白或胎球蛋白结合。重要的是,黏液曲霉可改善肠细胞单层完整性,如Caco-2细胞与细菌共培养的跨上皮电阻(TER)显着增加所表明的。此外,黏液曲霉诱导肠上皮细胞产生的白细胞介素8(IL-8)的浓度比大肠杆菌高100倍,表明上皮中促炎活性的水平非常低。总之,我们的结果表明,黏液曲霉可粘附于肠上皮并在体外增强肠上皮细胞单层完整性,这表明有能力增强受损的肠屏障。这些结果支持早期的体内联合研究,并提供了对黏液曲霉与宿主相互作用的见解。

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