CELL-ADHESION MOLECULES ACTING BETWEEN C6 GLIOMA AND ENDOTHELIAL-CELLS

被引:13
|
作者
TAMAKI, M
AOYAGI, M
MORITA, I
HIRAKAWA, K
MUROTA, SI
机构
[1] TOKYO MED & DENT UNIV,GRAD SCH,DEPT NEUROSURG,BUNKYO KU,TOKYO 113,JAPAN
[2] TOKYO MED & DENT UNIV,GRAD SCH,PHYSIOL CHEM SECT,TOKYO 113,JAPAN
关键词
CELL ADHESION MOLECULES; INVASION; C6 GLIOMA CELLS; BOVINE ENDOTHELIAL CELLS; ICAM-1; BETA(2) INTEGRIN;
D O I
10.1007/BF01078488
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The interactions between tumor cells and endothelium play a key role in the process of tumor growth, local invasion, and distant metastasis. In the present study, we examined the adhesion of C6 glioma cells to bovine endothelial cell (EC) monolayers and defined the cell adhesion molecules acting between these cells. Pretreatment of the EC monolayer with cytokines, tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and interferon (INF)-gamma, significantly increased the adhesion of C6 glioma cells to the EC monolayer. The effect lasted more than 24 hours and was protein-synthesis dependent. The adhesion of C6 glioma cells to TNF-activated ECs was blocked by the monoclonal antibody to the intercellular adhesion molecule-1 (ICAM-1) or beta(2) integrin, whereas that of melanoma cells was not. These findings provide evidence that ICAM-1 and beta(2) integrin function as inducible cell surface molecules that can support the adhesion of C6 glioma cells to ECs, and may contribute to the characteristic growth of glial tumors in vivo.
引用
收藏
页码:181 / 188
页数:8
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