FIBROBLAST GROWTH FACTOR-II CAN MEDIATE CELL ATTACHMENT BY LINKING RECEPTORS AND HEPARAN-SULFATE PROTEOGLYCANS ON NEIGHBORING CELLS

被引:53
作者
RICHARD, C
LIUZZO, JP
MOSCATELLI, D
机构
[1] NYU,MED CTR,DEPT CELL BIOL,NEW YORK,NY 10016
[2] NYU,MED CTR,KAPLAN CANC CTR,NEW YORK,NY 10016
关键词
D O I
10.1074/jbc.270.41.24188
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
The myeloid 32D cell line, which grows in suspension and does not express FGF receptors or heparan sulfate proteoglycans, was transfected with the cDNA encoding FGF receptor-1 (32D-flg cells), When co cultured with glutaraldehyde-fixed Chinese hamster ovary (CHO) cells, the 32D-flg cells remained in suspension in the absence of FGF-2 but attached to the CHO monolayer in the presence of 10 ng/ml FGF-2. In contrast, 32D cells transfected with the vector alone did not attach to the CHO monolayer in the presence of FGF-2, FGF-2-dependent attachment of 32D-flg cells was prevented by inclusion of 10 mu g/ml heparin in the incubation medium and was diminished when CHO mutants in glycosaminoglycan synthesis or wild-type CHO cells treated with heparinase were used, indicating that the attachment occurred through FGF-2 interactions with heparan sulfates on the CHO cells. Attachment of 32D-flg cells to wild-type CHO cells was half-maximal at 0.4 ng/ml FGF-2 and was also observed with FGF-1 but not FGF-4, 32D-flg cells also attached to living CHO cells in a FGF-S-dependent manner, but attachment was transient at 37 degrees C. Induction of new proteins was not required for FGF-2-dependent attachment, since attachment occurred when the co cultures were incubated at 4 degrees C and when the 32D-flg cells were preincubated with cycloheximide. FGF-2-dependent attachment of 32D-flg cells was also observed with Balb/C 3T3, NIH 3T3, and bovine capillary endothelial cells. We conclude that attachment is due to FGF-2 binding simultaneously to receptors on the 32D-flg cells and heparan sulfates on the CHO monolayers; thus, the FGF-P acts as a bridge between receptor-expressing cells and heparan sulfate-bearing cells. In addition, induction of DNA synthesis in 32D-flg cells in response to FGF-2 was potentiated by the CHO-associated heparan sulfates to the same extent as by soluble heparin, indicating that this interaction has functional significance.
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收藏
页码:24188 / 24196
页数:9
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