RECOMBINANT E-SELECTIN-PROTEIN MEDIATES TUMOR-CELL ADHESION VIA SIALYL-LEA AND SIALYL-LEX

被引:98
|
作者
MAJURI, ML [1 ]
MATTILA, P [1 ]
RENKONEN, R [1 ]
机构
[1] UNIV HELSINKI,DEPT BACTERIOL & IMMUNOL,HAARTMANINKATU 3,SF-00290 HELSINKI 29,FINLAND
关键词
D O I
10.1016/0006-291X(92)91885-T
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
E-selectin (previously known as ELAM-1) is one of the adhesion molecules expressed on activated endothelium. Here we show that HL-60 cells express sialyl-Lex, but not Sialyl-Lea on their surface, a colon carcinoma cell line COLO 205 express both these epitopes and another colon carcinoma COLO 320 does not express either one of them. HL-60 and COLO 205 cell adhere strongly to E-selectin coated microwells, whereas COLO 320 does not adhere at all to E-selectin. Finally we provide evidence that monoclonal anti-sialyl-Lex can abolish part of the adherence of HL-60 cells to recombinant E-selectin. The adherence of COLO 205 cells can be decreased by either monoclonal anti-sialyl-Lea or anti-sialyl-Lex antibodies. These results indicate that cell-associated sialylated carbohydrate moieties can act as ligands for recombinant E-selectin. © 1992.
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页码:1376 / 1382
页数:7
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