CD59 MOLECULE - A 2ND LIGAND FOR CD2 IN T-CELL ADHESION

被引:97
作者
DECKERT, M
KUBAR, J
ZOCCOLA, D
BERNARDPOMIER, G
ANGELISOVA, P
HOREJSI, V
BERNARD, A
机构
[1] FAC MED NICE, INSERM, U343, AVE VALOMBROSE, F-06107 NICE, FRANCE
[2] CZECHOSLOVAK ACAD SCI, INST MOLEC GENET, CS-11142 PRAGUE 1, CZECHOSLOVAKIA
关键词
D O I
10.1002/eji.1830221128
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T cell surface molecule CD2 forms, with its counter-receptor CD58 (LFA-3), a powerful adhesion/activation pathway. There is some evidence that CD2 might bind more than a single ligand. Chinese hamster ovary cells (CHO) expressing human CD59 after cDNA transfection (CD59+CHO) form rosettes with human T cells; these rosettes are inhibited in a dose-dependent fashion by the CD59 monoclonal antibody (mAb) H19 and by the CD2 mAb 0275 known to block natural rosettes, but not by the CD2R mAb D66, a poor rosette blocker. CD2+CHO transfectants form rosettes with human erythrocytes; these rosettes are inhibited by the CD59 mAb H19 in addition to CD2 mAb 0275 and CD58 mAb; murine thymoma cells expressing human CD2 form rosettes with CD59+CHO cells that again are blocked by CD59 H19 and by CD2 0275 mAb. In a marked contrast with H19, two others CD59 mAb, YTH 53.1 and MEM 43, which react with a different epitope on CD59, led to a 50 %-70 % increase of the number of cells forming rosettes. In addition to rosette experiments, the binding of I-125-labeled CD59 molecules to CD2+CHO cells was specifically inhibited by unlabeled CD59 molecule and CD2 mAb. Furthermore, the binding of CD59 molecules to resting T cells induced expression of CD2R epitopes. These results directly show that CD2 binds CD59 and that subtle molecular changes occur upon binding.
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页码:2943 / 2947
页数:5
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