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作 者:周卫东[1] 张鸿卿[1] 方敏 何琪扬 庞大本 薛绍白[1]
机构地区:[1]北京师范大学生物系
出 处:《药学学报》1996年第1期1-5,共5页Acta Pharmaceutica Sinica
基 金:国家自然科学基金;国家教委博士点基金
摘 要:利用Dotblot和流式细胞术,研究了分化诱导剂维甲酸,DMSO对HL-60细胞及其抗性亚型抗药性程度的影响,表明1μmol·ml^(-1)RA作用HL-60及其亚型24h,MDR1mRNA明显增高,但流式检测多药抗性细胞系对Rho-123的外排有所下降。2%DMSO作用HL-60及其亚型24h,流式细胞术检测显示各细胞系对Rho-123的外排明显增强,提示RA虽然提高MDR1基因的表达,但可能通过磷酸化/脱磷酸化方式抑制Pgp-170功能的表达,而DMSO能诱导完整功能的Pgp表达。Using dot blot hybridization and flowcytometry,the effects of differentiationinducers retinoic acid(RA)and dimethvl sulfoxide(DMSO)on the resistant level of HL-60 cells andits resistant subline cells were studied.When the cells were treated with RA 1 umol·L-1 for 24h,the expression of MDR 1 mRNA evidently increased in both HL-60 and its multidrug resistant sublinecells.The efflux of Rho-123 in the multidrug resistant subline cells was slightly decreased,But,whenthe cells were treated with 2%DMSO for 24 h the efflux of Rho-123 increased obviously.The resultssuggest that RA can induce the expression of MDR 1 gene but perhaps inhibit the function of pumpglycoprotein 170(Pgp-170)through phosphorylation/dephOsphorylation pathway.However,DMSOcould induce the expression of full function of Pgp。
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