首页> 外文OA文献 >Lactobacillus bulgaricus Prevents Intestinal Epithelial Cell Injury Caused by Enterobacter sakazakii-Induced Nitric Oxide both In Vitro and in the Newborn Rat Model of Necrotizing Enterocolitis▿
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Lactobacillus bulgaricus Prevents Intestinal Epithelial Cell Injury Caused by Enterobacter sakazakii-Induced Nitric Oxide both In Vitro and in the Newborn Rat Model of Necrotizing Enterocolitis▿

机译:保加利亚乳杆菌在体外和新生大鼠坏死性小肠结肠炎模型中均能预防阪崎肠杆菌诱导的一氧化氮引起的肠上皮细胞损伤▿

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摘要

Enterobacter sakazakii is an emerging pathogen that has been associated with outbreaks of necrotizing enterocolitis (NEC) as well as infant sepsis and meningitis. Our previous studies demonstrated that E. sakazakii induces NEC in a newborn rat model by inducing enterocyte apoptosis. However, the mechanisms responsible for enterocyte apoptosis are not known. Here we demonstrate that E. sakazakii induces significant production of nitric oxide (NO) in rat intestinal epithelial cells (IEC-6) upon infection. The elevated production of NO, which is due to increased expression of inducible NO synthase, is responsible for apoptosis of IEC-6 cells. Notably, pretreatment of IEC-6 cells with Lactobacillus bulgaricus (ATCC 12278) attenuated the upregulation of NO production and thereby protected the cells from E. sakazakii-induced apoptosis. Furthermore, pretreatment with L. bulgaricus promoted the integrity of enterocytes both in vitro and in the infant rat model of NEC, even after challenge with E. sakazakii. Infection of IEC-6 cells with E. sakazakii upregulated several genes related to apoptosis, cytokine production, and various signaling pathways, as demonstrated by rat gene array analysis, and this upregulation was subdued by pretreatment with L. bulgaricus. In agreement with these data, L. bulgaricus pretreatment protected newborn rats infected with E. sakazakii from developing NEC, resulting in improved survival.
机译:阪崎肠杆菌是一种新兴病原体,与坏死性小肠结肠炎(NEC)以及婴儿败血症和脑膜炎的爆发有关。我们以前的研究表明,阪崎肠杆菌通过诱导肠细胞凋亡来诱导新生大鼠模型中的NEC。但是,导致肠细胞凋亡的机制尚不清楚。在这里,我们证明了阪崎肠杆菌在感染后可诱导大鼠肠上皮细胞(IEC-6)中一氧化氮(NO)的大量产生。由于诱导型NO合酶表达的增加,NO产生的增加导致了IEC-6细胞的凋亡。值得注意的是,用保加利亚乳杆菌(ATCC 12278)预处理IEC-6细胞可减弱NO产生的上调,从而保护细胞免受阪崎肠杆菌诱导的细胞凋亡。此外,即使在用阪崎肠杆菌攻击后,用保加利亚乳杆菌进行的预处理仍能在体外和NEC幼鼠模型中促进肠上皮细胞的完整性。如大鼠基因阵列分析所示,阪崎肠杆菌感染IEC-6细胞会上调与凋亡,细胞因子产生和各种信号通路相关的几个基因,而保加利亚乳杆菌的预处理则抑制了这种上调。与这些数据一致,保加利亚乳杆菌预处理可以保护感染阪崎肠杆菌的新生大鼠免于发展NEC,从而提高生存率。

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