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首页> 外文期刊>Infection and immunity >Tumor necrosis factor alpha potentiates neutrophil antimicrobial activity: increased fungicidal activity against Torulopsis glabrata and Candida albicans and associated increases in oxygen radical production and lysosomal enzyme release.
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Tumor necrosis factor alpha potentiates neutrophil antimicrobial activity: increased fungicidal activity against Torulopsis glabrata and Candida albicans and associated increases in oxygen radical production and lysosomal enzyme release.

机译:肿瘤坏死因子α增强了中性粒细胞的抗微生物活性:增加了对光滑拟南芥和白色念珠菌的杀真菌活性,并增加了氧自由基的产生和溶酶体酶的释放。

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The capacity of human tumor necrosis factor alpha (TNF-alpha) to modulate the killing of the opportunistic pathogens Torulopsis glabrata and Candida albicans by human neutrophils was studied. TNF-alpha significantly enhanced neutrophil fungicidal activity in a concentration-dependent manner and was evident in a range of neutrophil-fungus ratios. Enhanced killing of T. glabrata required much lower TNF-alpha concentrations than were required for enhancement of killing of C. albicans. Maximal enhancement of killing occurred with 20 and 100 U of TNF-alpha per 5 x 10(6) neutrophils for T. glabrata and C. albicans, respectively. The fungal killing kinetics demonstrated that TNF-alpha augmentation of fungicidal activity was evident within 1 h and persisted for an incubation period of at least 22 h. Preincubation of neutrophils with TNF-alpha was essential for the enhancement of killing. Maximal stimulation of killing was observed within 1 h of preincubation with TNF-alpha, and poor stimulation of killing was observed when TNF-alpha was added at time zero. Associated with the increase in fungicidal activity was an increased production of superoxide and an enhanced degranulation of enzymes and other proteins from azurophilic and specific granules in response to the fungi. The results demonstrate that TNF-alpha augments the neutrophil oxidative respiratory burst and the degranulation induced by opsonized fungi and that it increases the neutrophil fungicidal activity.
机译:研究了人类肿瘤坏死因子α(TNF-α)调节人类嗜中性粒细胞杀死机会病原体光滑小球菌和白色念珠菌的能力。 TNF-α以浓度依赖的方式显着增强中性粒细胞的杀真菌活性,并且在一系列中性粒细胞-真菌比率中也很明显。与增加对白色念珠菌的杀灭作用所需的杀死作用相比,增强对光滑毛虫的杀灭作用所需要的TNF-α浓度要低得多。分别以每5 x 10(6)中性粒细胞20和100 U的TNF-α杀伤最大程度地增加了对T. glabrata和C. albicans的杀伤力。真菌的杀灭动力学表明,TNF-α杀真菌活性的增强在1小时内是明显的,并且持续至少22 h的潜伏期。中性粒细胞与TNF-α的预孵育对于增强杀伤力至关重要。在与TNF-α孵育前1小时内观察到最大的杀伤刺激作用,而在零时点添加TNF-α则观察到杀伤刺激作用很差。与杀真菌活性的增加相关的是,超氧化物的产生增加,并且响应于真菌,来自嗜铝和特异颗粒的酶和其他蛋白质的脱粒增强。结果表明,TNF-α增强了中性粒细胞的氧化呼吸爆发和调理真菌诱导的脱颗粒,并增加了中性粒细胞的杀真菌活性。

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