A flow cytometric assay for simultaneous assessment of drug efflux, proliferation, and apoptosis

被引:9
作者
Barbier, M
Gray, BD
Muirhead, KA
Ronot, X
Boutonnat, J [1 ]
机构
[1] EPHE, CNRS, UMR 5525, Lab Dynam Cellulaire,IBNS,Inst Albert Bonniot, F-38076 La Tronche, France
[2] PTI Res, Exton, PA USA
[3] SciGro, Malvern, PA USA
关键词
MDR; apoptosis; proliferation monitoring; PKH dyes; PTIR271;
D O I
10.1002/cyto.b.20004
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Proliferative status and multidrug resistance play a key role in determining cell response to chemotherapy. There is a need to develop multiple labeling method that allows simultaneous assessment of multidrug resistant (MDR) phenotype, proliferative status, apoptosis related changes in mitochondrial potential, in chemosensitive and chemoresistant tumor cell populations. Methods: A three-color labeling was performed using Hoechst 33342 (DNA), JC1 (mitochondrial potential), and a far red fluorescent membrane intercalating dye: PTIR271 (proliferation). Results: Combined staining of DNA and mitochondrial potential allows identification of subpopulations expressing and MDR phenotype mediated by P-glycoprotein (Pgp), and, in Pgp negative subpopulations, identification of apoptotic cells and evaluation of cell cycle status in viable cells. Addition of a far red fluorescent membrane intercalating dye, PTIR271, allows simultaneous monitoring of cell division status by dye dilution in both drug sensitive and drug resistant populations. Conclusion: This triple labeling is an interesting method to study the proliferation status of drug sensitivity and drug resistance in viable tumor cells. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:46 / 53
页数:8
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