Zaifert K, Cohen M C
Department of Microbiology and Immunology, Hahnemann University, Philadelphia, Pennsylvania 19102.
Clin Immunol Immunopathol. 1993 Jul;68(1):51-6. doi: 10.1006/clin.1993.1094.
We have demonstrated that pretreatment of human umbilical vein endothelial cells (HUVEC) with tumor necrosis factor-alpha (TNF) or phorbol myristate acetate (PMA) augmented the binding of COLO 205, a human colon carcinoma cell line, in vitro. The increased adherence was both concentration and time dependent with a peak for tumor cell attachment at 4 hr. The increase in binding required both RNA and protein synthesis. This pattern is consistent with increased expression of the adhesion molecule E-selectin (ELAM-1) on the endothelium. Incubation of TNF- or PMA-stimulated HUVEC with BB11, an anti-E-selectin mAb, prior to the addition of COLO 205, led to almost complete inhibition of adherence of the tumor cells. Flow cytometric analysis confirmed that there was expression of E-selectin on HUVEC following both TNF and PMA stimulation.
我们已经证明,用肿瘤坏死因子-α(TNF)或佛波酯(PMA)预处理人脐静脉内皮细胞(HUVEC)可增强人结肠癌细胞系COLO 205在体外的结合。增加的黏附具有浓度和时间依赖性,肿瘤细胞附着在4小时达到峰值。结合的增加需要RNA和蛋白质合成。这种模式与内皮细胞上黏附分子E-选择素(ELAM-1)表达增加一致。在添加COLO 205之前,用抗E-选择素单克隆抗体BB11孵育TNF或PMA刺激的HUVEC,几乎完全抑制了肿瘤细胞的黏附。流式细胞术分析证实,TNF和PMA刺激后HUVEC上有E-选择素表达。