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Lactobacillus plantarum Enhanced IL-22 Production in Natural Killer (NK) Cells That Protect the Integrity of Intestinal Epithelial Cell Barrier Damaged by Enterotoxigenic Escherichia coli

机译:Lactobacillus plantarum增强IL-22天然杀伤剂(NK)细胞的产生,可保护肠毒素大肠杆菌损坏的肠上皮细胞屏障的完整性

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摘要

Interleukin (IL)-22-producing Natural Killer (NK) cells protect the gut epithelial cell barrier from pathogens. A strain of probiotics, Lactobacillus plantarum (L. plantarum, LP), was previously found by our laboratory to significantly improve the mucosal barrier integrity and function of the small intestine in pigs. However, it was unclear whether LP benefited the intestinal mucosal barrier via interactions with the intestinal NK cells. The present study, therefore, was focused on the therapeutic effect of NK cells that were stimulated by LP on attenuating enterotoxigenic Escherichia coli (ETEC)-induced the damage to the integrity of the epithelial cell barrier. The results showed that LP can efficiently increase protein levels of the natural cytotoxicity receptor (NCR) family, and the expression levels of IL-22 mRNA and protein in NK cells. Transfer of NK cells stimulated by LP conferred protection against ETEC K88-induced intestinal epithelial barrier damage in NCM460 cells. We found that NK cells stimulated by LP could partially offset the reduction in NCM460 cell monolayers transepithelial electrical resistance (TEER) caused by ETEC K88, and increase ZO-1 and occludin mRNA and protein expressions by ETEC K88-infected NCM460 cells. Furthermore, adding NK cells that were stimulated by LP to ETEC K88-infected NCM460cells, IL-22R1, p-Stat3, and p-Tyk2 expression by NCM460 cells was increased. Mechanistic experiment showed that NK cells stimulated by LP lost the function of maintaining TEER of NCM460 cells challenged with ETEC K88, when polyclonal anti-IL-22 antibody was used to block IL-22 production. Collectively, our results suggested that LP stimulation of NK could enhance IL-22 production, which might be able to provide defense against ETEC-induced damage to the integrity of intestinal epithelial barrier.
机译:白细胞介素(IL)-22生产自然杀伤(NK)细胞保护从病原体的肠上皮细胞屏障。益生菌,植物乳杆菌(植物乳杆菌,LP),的菌株曾由我们的实验室发现显著改善猪小肠的粘膜屏障的完整性和功能。然而,目前还不清楚是否LP经由与肠NK细胞相互作用受益肠黏膜屏障。本研究中,因此,被集中在刺激通过LP上衰减肠毒素大肠杆菌(ETEC)诱导的上皮细胞屏障的完整性的损害NK细胞的治疗效果。结果表明,LP可以有效地增加NK细胞中天然细胞毒性受体(NCR)家族的蛋白水平,和IL-22 mRNA的表达水平和蛋白质。 NK细胞的转移刺激通过针对在NCM460细胞ETEC K88诱导的肠上皮屏障损伤唱片赋予的保护。我们发现,NK细胞刺激通过LP可以部分抵消造成的ETEC K88 NCM460细胞单层的跨上皮电阻(TEER)的减少,并且增加ZO-1和闭合蛋白通过ETEC K88感染NCM460细胞mRNA和蛋白表达。此外,该由LP通过NCM460细胞刺激ETEC K88感染NCM460cells,IL-22R1,对STAT3,和对表达的Tyk2加入NK细胞增加。机械试验表明,NK细胞刺激通过LP失去保持与ETEC K88,当多克隆抗IL-22抗体用于阻断IL-22生产的挑战NCM460细胞的TEER的功能。总的来说,我们的结果表明,NK的LP刺激可增强IL-22的产量,这可能是能够提供防御肠上皮屏障的完整性ETEC引起的损伤。

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