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Early administration of probiotic Lactobacillus acidophilus and/or prebiotic inulin attenuates pathogen-mediated intestinal inflammation and Smad 7 cell signaling

机译:早期施用益生菌乳杆菌和/或益生元菊粉衰减病原体介导的肠炎和Smad 7细胞信号传导

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摘要

Immaturity of gut-associated immunity may contribute to pediatric mortality associated with enteric infections. A murine model to parallel infantile enteric disease was used to determine the effects of probiotic, Lactobacillus acidophilus (La), prebiotic, inulin, or both (synbiotic, syn) on pathogen-induced inflammatory responses, NF-κB, and Smad 7 signaling. Newborn mice were inoculated bi-weekly for 4 weeks with La, inulin, or syn and challenged with Citrobacter rodentium (Cr) at 5 weeks. Mouse intestinal epithelial cells (CMT93) were exposed to Cr to determine temporal alterations in NF-Kappa B and Smad 7 levels. Mice with pretreatment of La, inulin, and syn show reduced intestinal inflammation following Cr infection compared with controls, which is associated with significantly reduced bacterial colonization in La, inulin, and syn animals. Our results further show that host defense against Cr infection correlated with enhanced colonic IL-10 and transforming growth factor-β expression and inhibition of NF-κB in syn-treated mice, whereas mice pretreated with syn, La, or inulin had attenuation of Cr-induced Smad 7 expression. There was a temporal Smad 7 and NF-κB intracellular accumulation post-Cr infection and post-tumor necrosis factor stimulation in CMT93 cells. These results, therefore, suggest that probiotic, La, prebiotic inulin, or synbiotic may promote host-protective immunity and attenuate Cr-induced intestinal inflammation through mechanisms affecting NF-κB and Smad 7 signaling.
机译:肠道相关免疫的不成熟可能有助于与肠道感染相关的儿科死亡率。用于平行婴儿肠疾病的小鼠模型用于确定益生菌,乳杆菌嗜酸杆菌(LA),益生元,菊粉或(Synbiotic,Syn)对病原体诱导的炎症反应,NF-κB和Smad 7信号传导的影响。 Newborn小鼠用La,菊粉或Syn接种双每周4周,并在5周时用柠檬酸杆菌(Cr)挑战。将小鼠肠上皮细胞(CMT93)暴露于CR以确定NF-Kappa B和Smad 7水平的时间改变。与La,菊粉和Syn预处理的小鼠显示CR感染后的肠炎症,与对照组相比,这与La,菊粉和SYN动物的细菌定植显着降低。我们的结果进一步表明,对CR感染的宿主防御与增强的结肠IL-10相关,转化生长因子-β表达和抑制NF-κB在合成的小鼠中,而用Syn,La或菊粉预处理的小鼠具有Cr的衰减 - 诱导的Smad 7表达。在CMT93细胞中存在颞下Smad 7和NF-κB细胞内积聚后Cr感染和肿瘤后坏死因子刺激。因此,这些结果表明,益生菌,洛杉矶,益生元菊蛋白或同步可以通过影响NF-κB和Smad 7信号传导的机制来促进宿主保护性免疫和衰减Cr诱导的肠炎。

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