首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Interaction of the Pseudomonas aeruginosa secretory products pyocyanin and pyochelin generates hydroxyl radical and causes synergistic damage to endothelial cells. Implications for Pseudomonas-associated tissue injury.
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Interaction of the Pseudomonas aeruginosa secretory products pyocyanin and pyochelin generates hydroxyl radical and causes synergistic damage to endothelial cells. Implications for Pseudomonas-associated tissue injury.

机译:铜绿假单胞菌分泌产物脓余素和脓余素的相互作用产生羟基自由基并对内皮细胞造成协同损伤。对假单胞菌相关组织损伤的影响。

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摘要

Pyocyanin, a secretory product of Pseudomonas aeruginosa, has the capacity to undergo redox cycling under aerobic conditions with resulting generation of superoxide and hydrogen peroxide. By using spin trapping techniques in conjunction with electron paramagnetic resonance spectrometry (EPR), superoxide was detected during the aerobic reduction of pyocyanin by NADH or porcine endothelial cells. No evidence of hydroxyl radical formation was detected. Chromium oxalate eliminated the EPR spectrum of the superoxide-derived spin adduct resulting from endothelial cell exposure to pyocyanin, suggesting superoxide formation close to the endothelial cell plasma membrane. We have previously reported that iron bound to the P. aeruginosa siderophore pyochelin (ferripyochelin) catalyzes the formation of hydroxyl free radical from superoxide and hydrogen peroxide via the Haber-Weiss reaction. In the present study, spin trap evidence of hydroxyl radical formation was detected when NADH and pyocyanin were allowed to react in the presence of ferripyochelin. Similarly, endothelial cell exposure to pyocyanin and ferripyochelin also resulted in hydroxyl radical production which appeared to occur in close proximity to the cell surface. As assessed by 51Cr release, endothelial cells which were treated with pyocyanin or ferripyochelin alone demonstrated minimal injury. However, endothelial cell exposure to the combination of pyochelin and pyocyanin resulted in 55% specific 51Cr release. Injury was not observed with the substitution of iron-free pyochelin and was diminished by the presence of catalase or dimethyl thiourea. These data suggest the possibility that the P. aeruginosa secretory products pyocyanin and pyochelin may act synergistically via the generation of hydroxyl radical to damage local tissues at sites of pseudomonas infection.
机译:绿脓杆菌(Pseudomonas aeruginosa)的分泌产物花青素具有在有氧条件下进行氧化还原循环的能力,从而产生超氧化物和过氧化氢。通过结合使用自旋捕集技术和电子顺磁共振波谱(EPR),在通过NADH或猪内皮细胞对绿藻素进行有氧还原过程中检测到超氧化物。没有检测到羟基自由基形成的证据。草酸铬消除了由于内皮细胞暴露于洋青霉素而产生的超氧化物衍生的自旋加合物的EPR谱,表明超氧化物在内皮细胞质膜附近形成。我们以前曾报道过,铁结合到铜绿假单胞菌的铁素体(ferripyochelin)会通过Haber-Weiss反应催化超氧化物和过氧化氢形成羟基自由基。在目前的研究中,当NADH和黄绿素在ferripyochelin的存在下反应时,检测到自旋陷阱证据表明羟基自由基的形成。相似地,内皮细胞暴露于绿脓素和铁氰菊酯也导致羟基自由基的产生,该羟基自由基的产生似乎发生在细胞表面附近。如通过51 Cr释放评估的那样,仅用绿脓素或铁氰菊酯处理的内皮细胞显示出最小的损伤。但是,内皮细胞暴露于pyochelin和pyyocyanin的组合会导致55%的特异性51Cr释放。用无铁的秋水仙素取代未观察到损伤,并且通过过氧化氢酶或二甲基硫脲的存在减少了损伤。这些数据表明铜绿假单胞菌分泌产物脓余素和脓毒素可能通过羟自由基的产生协同作用来破坏假单胞菌感染部位的局部组织。

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