A novel enhanced green fluorescent protein (EGFP)-K562 flow cytometric method for measuring natural killer (NK) cell cytotoxic activity

被引:32
作者
Kantakamalakul, W [1 ]
Jaroenpool, H
Pattanapanyasat, K
机构
[1] Mahidol Univ, Fac Med, Siriraj Hosp, Dept Microbiol, Bangkok 10700, Thailand
[2] Mahidol Univ, Fac Med, Siriraj Hosp, Ctr Excellence Flow Cytometry,Off Res & Dev, Bangkok 10700, Thailand
关键词
natural killer cell; cytotoxicity assay; flow cytometry; enhanced green fluorescent protein;
D O I
10.1016/S0022-1759(02)00505-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Enhanced green fluorescent protein (EGFP) was stably expressed in human erythroleukaemia K562 cells (EGFP-K562) and used as target cells for measurement of natural killer (NK) cell cytotoxicity by flow cytometty. The compromised EGFP-K562 target cells were stained with propidium iodide (PI) and showed dual (green-red) fluorescent. Although the kinetic study demonstrated that the optimal incubation time for the assay was 4 h, a 2-h incubation. period also gave comparable results. This new technique correlated strongly with the standard chromium (Cr-51) release assay at the correlation coefficients of 0.87 and 0.89 at p-value <0.001 for 2- and 4-h incubation times, respectively. The EGFP-K562 stable cell line provides a novel method to measure NK cytotoxicity by flow cytometry without pre-staining or pre-labeling target cells. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
相关论文
共 27 条
[1]   Green fluorescent protein variants as markers of retroviral-mediated gene transfer in primary hematopoietic cells and cell lines [J].
Bierhuizen, MFA ;
Westerman, Y ;
Visser, TP ;
Wognum, AW ;
Wagemaker, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 234 (02) :371-375
[2]   EUROPIUM-LABELED TARGET-CELLS IN AN ASSAY OF NATURAL-KILLER CELL-ACTIVITY .1. A NOVEL NONRADIOACTIVE METHOD BASED ON TIME-RESOLVED FLUORESCENCE [J].
BLOMBERG, K ;
GRANBERG, C ;
HEMMILA, I ;
LOVGREN, T .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 86 (02) :225-229
[3]  
BRUNNER KT, 1968, IMMUNOLOGY, V14, P181
[4]   CHARACTERIZATION OF EFFECTOR-TARGET CONJUGATES FOR CLONED HUMAN NATURAL-KILLER AND HUMAN LYMPHOKINE ACTIVATED KILLER-CELLS BY FLOW-CYTOMETRY [J].
CALLEWAERT, DM ;
RADCLIFF, G ;
WAITE, R ;
LEFEVRE, J ;
POULIK, MD .
CYTOMETRY, 1991, 12 (07) :666-676
[5]  
CHANG L, 1993, J IMMUNOL METHODS, V166, P45
[6]  
Cox JH, 1999, METH MOLEC MED, V17, P383, DOI 10.1385/0-89603-369-4:383
[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]   A novel method for measuring CTL and NK cell-mediated cytotoxicity using annexin V and two-color flow cytometry [J].
Goldberg, JE ;
Sherwood, SW ;
Clayberger, C .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 224 (1-2) :1-9
[9]   Stable expression of green fluorescent protein after liposomal transfection of K562 cells without selective growth conditions [J].
Gubin, AN ;
Koduru, S ;
Njoroge, JM ;
Bhatnagar, R ;
Miller, JL .
BIOTECHNIQUES, 1999, 27 (06) :1162-+
[10]  
HISERODT JC, 1982, J IMMUNOL, V129, P1782