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ExoU-induced redox imbalance and oxidative stress in airway epithelial cells during Pseudomonas aeruginosa pneumosepsis

机译:ExoU引起的铜绿假单胞菌肺炎性脓毒症气道上皮细胞氧化还原失衡和氧化应激

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ExoU is a potent proinflammatory toxin produced by Pseudomonas aeruginosa, a major agent of severe lung infection and sepsis. Because inflammation is usually associated with oxidative stress, we investigated the effect of ExoU on free radical production and antioxidant defense mechanisms during the course of P. aeruginosa infection. In an experimental model of acute pneumonia, ExoU accounted for increased lipid peroxidation in mice lungs as soon as 3 h after intratracheal instillation of PA103 P. aeruginosa strain. The contribution of airway cells to the generation of a redox imbalance was assessed by in vitro tests carried out with A549 airway epithelial cells. Cultures infected with the ExoU-producing PA103 P. aeruginosa strain produced significantly increased concentrations of lipid hydroperoxides, 8-isoprostane, reactive oxygen intermediates, peroxynitrite and nitric oxide (NO), when compared to cells infected with exoU-deficient mutants. Overproduction of NO by PA103-infected cells likely resulted from overexpression of both inducible and endothelial NO synthase isoforms. PA103 infection was also associated with a significantly increased activity of superoxide dismutase (SOD) and decreased levels of reduced glutathione (GSH), a major antioxidant compound. Our findings unveil another potential mechanism of tissue damage during infection by ExoU-producing P. aeruginosa strains.
机译:ExoU是一种由铜绿假单胞菌产生的有效促炎毒素,铜绿假单胞菌是严重肺部感染和败血症的主要药物。因为炎症通常与氧化应激相关,所以我们研究了铜绿假单胞菌感染过程中ExoU对自由基产生和抗氧化防御机制的影响。在急性肺炎的实验模型中,在气管内注入PA103铜绿假单胞菌菌株后3小时,ExoU导致小鼠肺中脂质过氧化增加。通过用A549气道上皮细胞进行的体外试验评估气道细胞对氧化还原失衡产生的贡献。与感染exoU缺陷突变体的细胞相比,感染产生ExoU的PA103铜绿假单胞菌菌株的培养物产生的脂质氢过氧化物,8-异前列腺素,活性氧中间体,过氧亚硝酸盐和一氧化氮(NO)浓度显着增加。 PA103感染的细胞过量产生NO可能是由于诱导型和内皮型NO合酶同工型的过表达所致。 PA103感染还与超氧化物歧化酶(SOD)的活性显着增加和主要抗氧化剂化合物还原型谷胱甘肽(GSH)的水平降低有关。我们的发现揭示了由ExoU产生的铜绿假单胞菌菌株感染期间组织损伤的另一种潜在机制。

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