首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Tilivalline- and Tilimycin-Independent Effects of Klebsiella oxytoca on Tight Junction-Mediated Intestinal Barrier Impairment
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Tilivalline- and Tilimycin-Independent Effects of Klebsiella oxytoca on Tight Junction-Mediated Intestinal Barrier Impairment

机译:产酸克雷伯菌对提利伐林和替利霉素的不依赖性对紧密连接介导的肠壁障碍的影响

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摘要

causes antibiotic-associated hemorrhagic colitis and diarrhea. This was attributed largely to its secreted cytotoxins tilivalline and tilimycin, inductors of epithelial apoptosis. To study whether exerts further barrier effects, T84 monolayers were challenged with bacterial supernatants derived from tilivalline/tilimycin-producing AHC6 or its isogeneic tilivalline/tilimycin-deficient strain Mut-89. Both preparations decreased transepithelial resistance, enhanced fluorescein and FITC-dextran-4kDa permeabilities, and reduced expression of barrier-forming tight junction proteins claudin-5 and -8. Laser scanning microscopy indicated redistribution of both claudins off the tight junction region in T84 monolayers as well as in colon crypts of mice infected with AHC6 or Mut-89, indicating that these effects are tilivalline/tilimycin-independent. Furthermore, claudin-1 was affected, but only in a tilivalline/tilimycin-dependent manner. In conclusion, induced intestinal barrier impairment by two mechanisms: the tilivalline/tilimycin-dependent one, acting by increasing cellular apoptosis and a tilivalline/tilimycin-independent one, acting by weakening the paracellular pathway through the tight junction proteins claudin-5 and -8.
机译:引起与抗生素有关的出血性结肠炎和腹泻。这主要归因于其分泌的细胞毒素tilivalline和tilimycin,它们是上皮细胞凋亡的诱导剂。为了研究是否发挥进一步的屏障作用,将T84单层细胞用源自提拉替林/产生替利霉素的AHC6或其同基因的提拉替林/替利霉素缺陷菌株Mut-89攻击的细菌上清液。两种制剂均降低了跨上皮的抵抗力,增强了荧光素和FITC-葡聚糖-4kDa的渗透性,并减少了形成屏障的紧密连接蛋白claudin-5和-8的表达。激光扫描显微镜观察表明,claudins在T84单层以及感染AHC6或Mut-89的小鼠的结肠隐窝的紧密连接区附近均发生了重新分布,表明这些作用是与tilivalline / tilimycin无关的。此外,claudin-1受到影响,但仅以对替利伐林/替利霉素的方式受到影响。总之,诱导肠屏障损伤的机制有两种:提洛伐林/替利霉素依赖的一种,其通过增加细胞凋亡起作用;和一种提洛夫林/替利霉素的非独立的,通过减弱紧密连接蛋白claudin-5和-8的旁细胞途径起作用。 。

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