汞和银离子对人多形核白细胞超氧阴离子产生的刺激作用。

G Jansson, M Harms-Ringdahl
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引用次数: 62

摘要

在一项重金属离子对人类多形核白细胞(中性粒细胞)氧化代谢(呼吸爆发)影响的调查中,我们发现汞(II)和银离子在微摩尔浓度下显著增加细胞中超氧阴离子的产生,由甲酰-蛋氨酸-leucylphenylalanine (fMLP)引发。从不同的献血者分离的细胞中,由一定离子浓度诱导的自由基形成的刺激有很大的不同,从适度增加到非常大(高达控制值的400%)。可溶性刺激剂肉豆酸酯佛波酯(PMA)或颗粒性刺激剂Zymosan触发细胞呼吸爆发时,未观察到金属离子对超氧阴离子形成的额外刺激作用。这一事实可能表明,金属离子对fmlp依赖性细胞活性启动的影响是一种与趋化肽及其在细胞表面的相应受体分子相互作用耦合的机制。通过在静止中性粒细胞的预孵育期间增加银离子的浓度,可以在浓度超过5微米时记录细胞的自发活化。然而,在不同供者的血液样本中,发生这种自发呼吸爆发的银离子浓度差异很大,浓度范围为5至15微米。由于汞离子在5微米以上具有毒性,因此对汞离子没有这种影响。一些献血者的血液样本中含有中性粒细胞,它们可以被低至1微米浓度的汞离子或银离子激活。中性粒细胞在银离子浓度升高时的自发活化在动力学上与pma诱导的相似。在超氧阴离子形成开始之前有一个滞后期,其长度随施用于细胞的药剂浓度而变化。众所周知,一旦中性粒细胞被fMLP激活,就不可能通过第二次补充fMLP来重新激活细胞。然而,在fmlp诱导的活化停止后,PMA或银离子的加入会引起超氧阴离子的重新产生。我们提出了银离子对中性粒细胞氧化代谢的两种不同作用机制。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stimulating effects of mercuric- and silver ions on the superoxide anion production in human polymorphonuclear leukocytes.

In a survey of a number of heavy metal ions for effects on the oxidative metabolism (respiratory burst) of human polymorphonuclear leukocytes (neutrophils) we have found that mercury(II) and silver ions in micromolar concentration significantly increase the production of superoxide anions in cells, initiated by formyl-methionyl-leucylphenylalanine (fMLP). The stimulation of radical formation induced by a certain ion concentration varied considerably in cells isolated from different blood donors, from a moderate increase to a very large (up to 400% of control values). When the soluble stimulator phorbol myristate acetate (PMA) or the particulate stimulator Zymosan were used to initiate the cell respiratory burst, no additional stimulating effects by the metal ions on superoxide anion formation were observed. This fact might indicate that the effect of the metal ions on the fMLP-dependent initiation of cell activity is a mechanism coupled to the interaction between the chemotactic peptide and its corresponding receptor molecules on the cell surface. By increasing the concentration of silver ions during pre-incubation of resting neutrophils, a spontaneous activation of the cells could be recorded at a concentration exceeding 5 microM. However, the silver ion concentration at which such spontaneous initiation of the respiratory burst occurred varied significantly between blood samples from different donors with a concentration range of 5 to 15 microM. This effect could not be shown for mercuric ions due to the toxicity of the metal above 5 microM. Blood samples from some donors contained neutrophils that could be activated by either mercuric- or silver ions at concentration as low at 1 microM. The spontaneous activation of neutrophils with elevated concentrations of silver ions is kinetically similar to the PMA-induced. The onset of superoxide anion formation is preceded by a lag period whose length varies in time with the concentration of agent applied to the cells. It is a known fact that once the neutrophils have been activated with fMLP it is not possible to reactivate the cells by a second supplementation of fMLP. However, after cessation of the fMLP-induced activation, addition of PMA or silver ions gives rise to renewed production of superoxide anions. We propose two different mechanisms of action of silver ions on oxidative metabolism of neutrophils.(ABSTRACT TRUNCATED AT 400 WORDS)

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