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Hydrogen peroxide and superoxide modulate leukocyte adhesion molecule expression and leukocyte endothelial adhesion

机译:过氧化氢和超氧化物调节白细胞粘附分子表达和白细胞内皮粘附

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摘要

While endothelial oxidant generation and subsequent leukocyte chemotaxis and activation are important mechanisms of tissue damage in ischemie organs, it is not known if oxidant generation may be involved in triggering the subsequent leukocyte-mediated injury which occurs. Questions remain whether particular oxidants and oxygen-free radicals are capable of modulating the expression of leukocyte adhesion molecules and effecting leukocyte endothelial adhesion. Studies were performed to determine the effect of different biologically occurring oxidant molecules and oxygen free radicals including: -O^, 'OH, and H2O2 on the expression of integrin and selectin adhesion molecules on the surface of human PMNs and to determine the effect of these alterations on PMN adhesion to the endothelium. Adhesion molecule expression on the surface of human PMNs was measured by immunofluorescence flow cytometry. Electron paramagnetic resonance spectroscopy was applied to characterize the presence of exogenous free radical generation as well as that from activated PMNs. It was observed that these oxidants can cause up-regulation of CD1 lb and CD18 expression with shedding of L-selectin. The kinetics and dose-response of these effects were analyzed and their functional significance determined by measuring PMN adhesion to cultured human aortic endothelial monolayers. These studies demonstrate that oxygen free radicals and non-radical oxidants can directly trigger PMN activation and adhesion to vascular endothelium.
机译:尽管内皮氧化剂的产生以及随后的白细胞趋化性和活化是缺血器官中组织损伤的重要机制,但尚不知道氧化剂的产生是否与引发随后发生的白细胞介导的损伤有关。仍然存在问题,即特定的氧化剂和氧自由基是否能够调节白细胞粘附分子的表达并影响白细胞内皮粘附。进行了研究以确定不同的生物氧化剂分子和氧自由基(包括-O ^,'OH和H2O2)对人PMN表面上整联蛋白和选择素粘附分子表达的影响,并确定这些影响PMN粘附到内皮的改变。通过免疫荧光流式细胞术测量人PMN表面上的粘附分子表达。应用电子顺磁共振波谱法表征外源自由基的产生以及活化PMN的产生。观察到这些氧化剂可导致L-选择蛋白脱落而引起CD11b和CD18表达的上调。分析了这些作用的动力学和剂量反应,并通过测量PMN对培养的人主动脉内皮细胞单层的粘附力来确定其功能意义。这些研究表明,氧自由基和非自由基氧化剂可以直接触发PMN活化并粘附至血管内皮。

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