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首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Effect of S-(1,2-dicarboxyethyl) glutathione and S-(1,2-dicarboxyethyl) cysteine on the stimulus-induced superoxide generation and tyrosyl phosphorylation of proteins in human neutrophils.
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Effect of S-(1,2-dicarboxyethyl) glutathione and S-(1,2-dicarboxyethyl) cysteine on the stimulus-induced superoxide generation and tyrosyl phosphorylation of proteins in human neutrophils.

机译:S-(1,2-二羧乙基)谷胱甘肽和S-(1,2-二羧乙基)半胱氨酸对刺激诱导的人中性粒细胞蛋白质超氧化物生成和酪氨酰磷酸化的影响。

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摘要

We investigated the effects of S-(1,2-dicarboxyethyl) glutathione (DCEG) and S-(1,2-dicarboxyethyl) cysteine (DCEC) on the stimulus-induced superoxide generation and tyrosyl phosphorylation of proteins in human neutrophils. When the cells were preincubated with DCEG, the superoxide generation induced by N-formyl-methionyl-leucyl-phenylalanine (fMLP) was enhanced in concentration-dependent manner but DCEC showed no effect. The influence of DCEG and DCEC on phorbol 12-myristate 13-acetate-induced superoxide generation showed no effect. On the other hand, the superoxide generation induced by arachidonic acid was markedly suppressed by DCEG and DCEC in concentration-dependent manner. The suppression of DCEG was more effective than that of DCEC. The superoxide generation induced by fMLP in the DCEG-treated cells was suppressed by genistein. DCEG enhanced tyrosyl phosphorylation of 80.0 kDa, 60.0 kDa, and 45.0 kDa proteins in human neutrophils. The tyrosyl phosphorylation of 80.0 kDa, 60.0 kDa, and 45.0 kDa proteins was suppressed by genistein. The enhancement of tyrosyl phosphorylation of these proteins in the DCEG-treated cells was parallel to the enhancement of the fMLP-induced superoxide generation.
机译:我们调查了S-(1,2-二羧乙基)谷胱甘肽(DCEG)和S-(1,2-二羧乙基)半胱氨酸(DCEC)对人中性粒细胞中蛋白质诱导的超氧化物生成和酪氨酰磷酸化的影响。当将细胞与DCEG预孵育时,N-甲酰基-甲硫酰基-亮氨酰-苯丙氨酸(fMLP)诱导的超氧化物生成以浓度依赖的方式增强,但DCEC却没有作用。 DCEG和DCEC对佛波醇12-肉豆蔻酸酯13-乙酸酯诱导的超氧化物生成没有影响。另一方面,DCEG和DCEC以浓度依赖的方式显着抑制了花生四烯酸诱导的超氧化物的产生。抑制DCEG比抑制DCEC更有效。金雀异黄素抑制了fMLP在DCEG处理的细胞中诱导的超氧化物生成。 DCEG增强了人类嗜中性粒细胞中80.0 kDa,60.0 kDa和45.0 kDa蛋白的酪氨酰磷酸化。金雀异黄素抑制了80.0 kDa,60.0 kDa和45.0 kDa蛋白的酪氨酰磷酸化。这些蛋白质在DCEG处理的细胞中酪氨酰磷酸化的增强与fMLP诱导的超氧化物生成的增强平行。

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