Determination of T-lymphocyte adhesion to endothelial cells using a novel luminescence marker

被引:2
|
作者
Termeer, CC [1 ]
Weiss, JM [1 ]
Dittmar, H [1 ]
Vanscheidt, W [1 ]
Schopf, E [1 ]
Simon, JC [1 ]
机构
[1] Univ Freiburg, Dept Dermatol, D-79104 Freiburg, Germany
来源
IMMUNOTECHNOLOGY | 1998年 / 3卷 / 04期
关键词
adhesion-assay; luminescence marker; T cell; endothelial cell; ICAM-1; LFA-1;
D O I
10.1016/S1380-2933(97)10001-X
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Here we report the quantification of T cell adhesion to endothelial cells using the luminescence marker BioLite(TM). A new application for this substance was established using a microassay for the detection of TK-1 mouse T-lymphoma cell adhesion to unstimulated or TNF alpha-stimulated eEnd.2 mouse vascular endothelioma cells. Prelabelling of TK-1 with the marker resulted in luminescence values linearly related to the number of adherent T cells. The marker was not toxic for T cells or endothelial cells nor did it interfere with the expression or function of adhesion molecules on T cells (LFA-1, VLA-4) or endothelial cells (ICAM-1, VCAM-1). When compared with established techniques to quantify T cell/endothelial cell adhesion, i.e. microscopical evaluation or isotope prelabelling of T cells, this method was found to be just as reliable and sensitive. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:245 / 252
页数:8
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