Frey T, Yue S, Haugland R P
Becton Dickinson Immunocytometry System, San Jose, California 95131, USA.
Cytometry. 1995 Jul 1;20(3):218-27. doi: 10.1002/cyto.990200305.
In an effort to improve detection of P-glycoprotein-mediated multidrug resistance (mdr), several dyes were compared to rhodamine 123 (R123) in efflux assays. Two dyes (SY-38 and SY-3150) were found that provided better sensitivity. These dyes were effluxed by a cell line known to be mdr-positive (P388/R84) but not by an mdr-negative cell line (P388). Efflux was blocked by both verapamil and cyclosporine A. Efflux from KG1a cells was less than from P388/R84, just as has been seen with R123 and daunomycin. In further experiments, a model system was used to demonstrate two-color immunofluorescence plus efflux measurements. This was done using a sequential staining method. A procedure was devised that, at least for this model system, allowed single-step staining with both dye and antibody. The sensitivity of the efflux measurement was slightly compromised by using this one-step staining method.
为了提高对P-糖蛋白介导的多药耐药性(mdr)的检测,在流出试验中,将几种染料与罗丹明123(R123)进行了比较。发现两种染料(SY-38和SY-3150)具有更高的灵敏度。已知mdr阳性细胞系(P388/R84)可使这些染料流出,但mdr阴性细胞系(P388)则不能。维拉帕米和环孢素A均可阻断流出。KG1a细胞的流出少于P388/R84细胞,正如R123和柔红霉素的情况一样。在进一步的实验中,使用一个模型系统来演示双色免疫荧光加流出测量。这是通过顺序染色法完成的。设计了一种程序,至少对于这个模型系统,允许染料和抗体一步染色。使用这种一步染色法,流出测量的灵敏度略有下降。