A novel flow cytometric assay for quantitation and multiparametric characterization of cell-mediated cytotoxicity

被引:182
作者
Lecoeur, H
Février, M
Garcia, S
Rivière, Y
Gougeon, ML
机构
[1] Inst Pasteur, Dept SIDA & Retrovirus, URA CNRS 1930, Unite Oncol Virale, F-75724 Paris 15, France
[2] Inst Pasteur, Dept SIDA & Retrovirus, URA CNRS 1930, Lab Immunopathol Virale, F-75724 Paris, France
关键词
cytotoxicity; flow cytometry; phenotyping; CFSE; 7-AAD;
D O I
10.1016/S0022-1759(01)00359-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cell-mediated cytotoxicity is a crucial mechanism involved in several fundamental immunological processes such as protection against intracellular pathogens or termination of an immune response. This phenomenon is classically evaluated by the Cr-51 release assay, which requires a radioactive isotope and does not permit the characterization of cells involved in the cytotoxic reaction. We describe a new flow cytometry method, developed in the context of CD95-mediated cell death, which allows the precise quantitation of cell-mediated cytotoxicity and the detection of intracellular events involved in the cytotoxic process. This assay uses a combination of two dyes. i.e. 5- (and 6-) carboxyfluorescein diacetate succinimydyl ester (CFSE) to label effector cells and 7-amino actinomycin D (7-AAD) to stain apoptotic target cells. We show that this assay is more sensitive than the Cr-51 release assay and makes it possible to quantitate the percentage of cell lysis and, concomitantly, to immunophenotype target cells. It also facilitates the analysis of some events of the apoptotic pathway such as caspase activation or the expression of mitochondrial molecules. This new assay should contribute to a better understanding of the mechanisms involved in cell-mediated cytotoxicity in normal and pathological situations. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 187
页数:11
相关论文
共 32 条
[1]  
Belloc F, 2000, CYTOMETRY, V40, P151, DOI 10.1002/(SICI)1097-0320(20000601)40:2<151::AID-CYTO9>3.0.CO
[2]  
2-9
[3]  
BRUNNER KT, 1968, IMMUNOLOGY, V14, P181
[4]   GAG-SPECIFIC CYTOTOXIC T-LYMPHOCYTES FROM HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1-INFECTED INDIVIDUALS - GAG EPITOPES ARE CLUSTERED IN 3 REGIONS OF THE P24GAG PROTEIN [J].
BUSEYNE, F ;
MCCHESNEY, M ;
PORROT, F ;
KOVARIK, S ;
GUY, B ;
RIVIERE, Y .
JOURNAL OF VIROLOGY, 1993, 67 (02) :694-702
[5]  
CHANG L, 1993, J IMMUNOL METHODS, V166, P45
[6]  
Depraetere V, 1997, Semin Immunol, V9, P93, DOI 10.1006/smim.1997.0062
[7]   A NOVEL NONRADIOACTIVE CELLULAR CYTOTOXICITY TEST BASED ON THE DIFFERENTIAL-ASSESSMENT OF LIVING AND KILLED TARGET AND EFFECTOR-CELLS [J].
FLIEGER, D ;
GRUBER, R ;
SCHLIMOK, G ;
REITER, C ;
PANTEL, K ;
RIETHMULLER, G .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 180 (01) :1-13
[8]   Potential deleterious effect of anti-viral cytotoxic lymphocyte through the CD95 (FAS/APO-1)-mediated pathway during chronic HIV infection [J].
Garcia, S ;
Fevrier, M ;
Dadaglio, G ;
Lecoeur, H ;
Riviere, Y ;
Gougeon, ML .
IMMUNOLOGY LETTERS, 1997, 57 (1-3) :53-58
[9]   Following the development of a CD4 T cell response in vivo: From activation to memory formation [J].
Garcia, S ;
DiSanto, J ;
Stockinger, B .
IMMUNITY, 1999, 11 (02) :163-171
[10]   A novel method for the simultaneous assessment of natural killer cell conjugate formation and cytotoxicity at the single-cell level by multi-parameter flow cytometry [J].
Godoy-Ramirez, K ;
Franck, K ;
Gaines, H .
JOURNAL OF IMMUNOLOGICAL METHODS, 2000, 239 (1-2) :35-44