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作 者:浦津[1] 楼方定[1] 周绮[1] 张苗[1] 史子江[1]
机构地区:[1]中国人民解放军总医院血液科
出 处:《中华医学杂志》1999年第3期224-226,共3页National Medical Journal of China
基 金:军队九五攻关重点基金
摘 要:目的探讨环孢菌素A(CsA)联合细胞因子对耐药细胞系K562/A02的逆转作用。方法以甲基四唑蓝法测定柔红霉素(DNR)的细胞毒性;用流式细胞仪技术测定细胞内罗丹明(Rh123)浓度;用RTPCR及JSB1抗体分别检测多药耐药(MDR1)mRNA及其P糖蛋白的表达。结果1μmol/LCsA、500U/ml干扰素、200U/ml白介素2(IL2)均能增加DNR对耐药细胞系K562/A02的细胞毒作用,IC50(半抑制浓度)分别为(3.78±0.03)μg/ml,(13.77±0.38)μg/ml,(18.5±0.60)μg/ml,逆转倍数分别为6.70、1.84和1.37倍。而上述剂量的CsA和IFNα联合则IC50为(1.71±0.19)μm/ml,逆转倍数增加到14.8倍,且细胞内Rh123浓度亦明显高于单药逆转(P<0.05),但MDR1mRNA及P糖蛋白表达无明显改变。CsA和IL2联合应用无明显的协同效应。结论单用低剂量CsA(1μmol/L)或细胞因子对多药耐药只有部分逆转作用,而CsA联合干扰素则有较好的协同效应,能明显增强耐药的逆转作用。Objective To explore the reversal effect of cyclosporin A(CsA) in combination with cytokines on multidrug resistant cell line K562/A02. Method The cytotoxicities of daunorubicin(DNR) were assayed by MTT method. Intracellular rhodamine(Rh123) concentration was measured by flow cytometry. P glycoprotein(p gp) expression was analyzed for staining with monoclonal JSB 1. Mdr1 mRNA expression was detected by RT PCR.Results The cytotoxicities of DNR to K562/A02 were enhanced by 1μmol/L CsA, 500U/ml、IFN α and 200U/ml、IL 2 respectively, and their IC 50 was (3.78±0.03), (13.77±0.38) μ/ml, (18.5±0.60)μg/ml. Their reversal effect was 6.70, 1.84 and 1.37 times than that of K562/A02. But IC 50 of combined CsA and IFN α was (1.71±0.19) μg/ml; its reverse effect increased in 14.8 times. The combination could increase intracellular Rh123 accumulation significantly as compared with either of them alone, but p gp and mdr1 mRNA expression were not decreased obviously. CsA in combination with IL 2 didn′t show a synergistic effect.Conclusion Mdr could be partially reversed by cytokines or low doses CsA(1 μmol/L), but the combination of CsA and IFN α showed a greater synergistic reversal interaction.
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