Effect of ethanol on natural killer cell activity in vitro.

S F Luo, C T Liu
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Abstract

The effect of ethanol on kinetic stages of natural killer (NK) cell activity was studied in vitro. Peripheral blood mononuclear cells (MNC) were either co-cultured or pre-incubated with various ethanol concentrations and assayed for NK cell activity with a "4-hour chromium release assay" and a "single cell cytotoxicity assay in agarose" simultaneously. Direct addition of ethanol to the assay system resulted in a dose-dependent inhibition of NK cell activity. The percentage of lysed conjugated target cells was suppressed from a control value of 21.2% to 17.0%, 15.1%, 11.8% and 10.0% with an ethanol concentration of 0.125%, 0.25%, 0.5% and 1.0%, respectively. NK cell recycling was also inhibited. A 24-hour pre-incubation with ethanol, however, resulted in NK cell activity enhancement. The enhancement was around 20% with a 0.25% ethanol concentration and around 45% with a 0.5% and a 1.0% ethanol concentrations. The enhancing effect was noted mainly at the cytolysis stage after binding of effector cell with target cells.

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乙醇对体外自然杀伤细胞活性的影响。
在体外研究了乙醇对NK细胞活性动力学阶段的影响。外周血单核细胞(MNC)与不同浓度的乙醇共培养或预孵育,同时用“4小时铬释放试验”和“琼脂糖单细胞毒性试验”检测NK细胞活性。直接添加乙醇到检测系统导致NK细胞活性的剂量依赖性抑制。当乙醇浓度分别为0.125%、0.25%、0.5%和1.0%时,结合靶细胞的裂解率从控制值21.2%降至17.0%、15.1%、11.8%和10.0%。NK细胞再循环也受到抑制。然而,用乙醇预孵育24小时,导致NK细胞活性增强。当乙醇浓度为0.25%时,增强幅度约为20%;当乙醇浓度为0.5%和1.0%时,增强幅度约为45%。增强作用主要发生在效应细胞与靶细胞结合后的细胞溶解阶段。
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