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Luminol-amplified chemiluminescence detects mainly superoxide anion produced by human neutrophils

机译:鲁米诺扩增的化学发光主要检测人嗜中性粒细胞产生的超氧阴离子

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摘要

Reactive oxygen species (ROS) are produced by numerous biological systems and by several phagocytes such as neutrophils and macrophages. ROS include mostly superoxide anion, hydrogen peroxide, singlet oxygen and hydroxyl radical, which are involved in a variety of biological processes such as immunity, inflammation, apoptosis and cell signaling. Thus, there is a need for a sensitive and reliable method to measure ROS. The luminol-amplified chemiluminescence technique is widely used to measure ROS production by neutrophils; however, it is unclear which ROS species are detected by this technique. In this study, we show that Xanthine/Xanthine oxidase (XXO), a known superoxide-producing system, stimulated a luminol-amplified chemiluminescence in the absence of horseradish peroxidase (HRPO), while the presence of HRPO enhanced the response. Both reactions were inhibited by superoxide dismutase (SOD), but not by catalase, confirming that superoxide anion, and not hydrogen peroxide, is the species oxidizing luminol to produce chemiluminescence. Glucose/Glucose oxidase (GGO), a known hydrogen peroxide-producing system, did not induce luminol-amplified chemiluminescence in the absence of HRPO; however, addition of HRPO resulted in a chemiluminescence response, which was inhibited by catalase, but not by SOD. Myeloperoxidase (MPO), isolated from human neutrophils, was also able to enhance the superoxide- and hydrogen peroxide-dependent luminol-amplified chemiluminescence. The production of ROS by stimulated human neutrophils was detected by luminol-amplified chemiluminescence, which was only partially inhibited by SOD and catalase. Interestingly, adding HRPO to stimulated neutrophils increased the luminol-amplified chemiluminescence, which was strongly inhibited by SOD, but not by catalase. These results show that (a) luminol-amplified chemiluminescence is able to detect superoxide anion in the absence of peroxidases, but not hydrogen peroxide; (b) in the presence of peroxidases, luminol-amplified chemiluminescence is able to detect both superoxide anion and hydrogen peroxide; and (c) luminol-amplified chemiluminescence detects mainly superoxide anion produced by neutrophils, especially in the presence of HRPO.
机译:活性氧(ROS)是由许多生物系统和吞噬细胞(如嗜中性粒细胞和巨噬细胞)产生的。 ROS主要包括超氧阴离子,过氧化氢,单线态氧和羟基自由基,它们参与各种生物过程,例如免疫,炎症,凋亡和细胞信号传导。因此,需要一种灵敏且可靠的方法来测量ROS。鲁米诺放大化学发光技术被广泛用于测量嗜中性粒细胞产生的ROS。然而,目前尚不清楚该技术可检测到哪些ROS。在这项研究中,我们显示了黄嘌呤/黄嘌呤氧化酶(XXO),一种已知的超氧化物生成系统,在没有辣根过氧化物酶(HRPO)的情况下刺激了鲁米诺放大的化学发光,而HRPO的存在增强了响应。两种反应均受到超氧化物歧化酶(SOD)的抑制,但不受过氧化氢酶的抑制,这证实了超氧化物阴离子而不是过氧化氢是氧化鲁米诺以产生化学发光的物质。在没有HRPO的情况下,葡萄糖/葡萄糖氧化酶(GGO)是一种已知的产生过氧化氢的系统,不会诱导鲁米诺增强的化学发光。但是,添加HRPO会导致化学发光反应,该反应被过氧化氢酶抑制,但未被SOD抑制。从人类嗜中性粒细胞中分离出来的髓过氧化物酶(MPO)也能够增强过氧化物和过氧化氢依赖性鲁米诺扩增的化学发光。鲁米诺扩增的化学发光检测了受刺激的人中性粒细胞产生的ROS,而SOD和过氧化氢酶仅部分抑制了ROS的产生。有趣的是,在刺激的嗜中性粒细胞中加入HRPO可以增强Luminol扩增的化学发光,这种化学发光强烈地被SOD抑制,但不被过氧化氢酶抑制。这些结果表明:(a)在没有过氧化物酶但没有过氧化氢的情况下,鲁米诺扩增的化学发光能够检测超氧阴离子; (b)在存在过氧化物酶的情况下,鲁米诺放大的化学发光能够检测超氧阴离子和过氧化氢; (c)鲁米诺放大的化学发光法主要检测中性粒细胞产生的超氧阴离子,尤其是在存在HRPO的情况下。

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