Lankelma J, Spoelstra E C, Dekker H, Broxterman H J
Free University Hospital, Department of Oncology, Amsterdam, The Netherlands.
Biochim Biophys Acta. 1990 Dec 10;1055(3):217-22. doi: 10.1016/0167-4889(90)90035-c.
Using a flow-through system human multidrug-resistant 2780AD ovarian carcinoma cells were exposed to flowing culture medium containing the anticancer agent daunomycin (5 microM). A pulse of medium containing verapamil caused increased cellular daunomycin accumulation, resulting in a dip in the fluorescence signal from daunomycin in the effluent. After passage of this pulse we observed an efflux of more than 90% of this extra accumulated daunomycin within 10 min. This daunomycin efflux against a concentration gradient provides evidence for drug efflux from these cells being an active process. After the addition of methylamine to the medium to increase intravesicular pH, the dip in the fluorescence signal was not decreased, indicating that vesicular transport was not an important component of this efflux.
使用流通系统,将人多药耐药2780AD卵巢癌细胞暴露于含有抗癌药物柔红霉素(5微摩尔)的流动培养基中。含有维拉帕米的培养基脉冲导致细胞内柔红霉素积累增加,从而使流出液中柔红霉素的荧光信号下降。在这个脉冲通过后,我们观察到在10分钟内,超过90%的额外积累的柔红霉素流出。这种逆浓度梯度的柔红霉素流出为这些细胞的药物流出是一个主动过程提供了证据。在培养基中加入甲胺以提高囊泡内pH值后,荧光信号的下降并未减少,这表明囊泡运输不是这种流出的重要组成部分。