Iademarco M F, McQuillan J J, Rosen G D, Dean D C
Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
J Biol Chem. 1992 Aug 15;267(23):16323-9.
Vascular cell adhesion molecule-1 (VCAM-1) was first identified as a protein that appears on the surface of endothelial cells after exposure to inflammatory cytokines. Through interaction with its integrin counter receptor VLA-4, VCAM-1 mediates cell-cell interactions important for immune function. We have cloned and begun characterization of the promoter for the VCAM-1 gene. In a series of transfection assays into human umbilical vein endothelial cells (HUVECs), we find that silencers between positions -1.641 kilobases and -288 base pairs restrict promoter activity, and that treatment with tumor necrosis factor-alpha overcomes this inhibition and activates the promoter through two NF kappa B sites located at positions -77 and -63 base pairs of the VCAM-1 gene. This responsiveness appears cell-specific since constructs containing the VCAM-1 NF kappa B sites are not responsive to tumor necrosis factor alpha in the T-cell line Jurkat. The two VCAM-1 NF kappa B sites, which differ slightly in their sequence, form distinct complexes in gel retardation assays, suggesting that they interact with different NF kappa B-site binding proteins. The distribution of these proteins could then control activity of the NF kappa B sites. We conclude that the pattern of VCAM-1 expression in HUVECs is controlled by a combination of these silencers and NF kappa B sites.
血管细胞黏附分子-1(VCAM-1)最初被鉴定为一种在内皮细胞暴露于炎性细胞因子后出现在其表面的蛋白质。通过与整合素配体VLA-4相互作用,VCAM-1介导对免疫功能重要的细胞间相互作用。我们已经克隆并开始对VCAM-1基因的启动子进行表征。在一系列对人脐静脉内皮细胞(HUVECs)的转染实验中,我们发现位于-1.641千碱基和-288碱基对之间的沉默子会限制启动子活性,而用肿瘤坏死因子-α处理可克服这种抑制作用,并通过位于VCAM-1基因-77和-63碱基对位置的两个核因子κB(NFκB)位点激活启动子。这种反应性似乎具有细胞特异性,因为含有VCAM-1 NFκB位点的构建体在T细胞系Jurkat中对肿瘤坏死因子-α无反应。两个VCAM-1 NFκB位点在序列上略有不同,在凝胶阻滞实验中形成不同的复合物,这表明它们与不同的NFκB位点结合蛋白相互作用。这些蛋白质的分布进而可以控制NFκB位点的活性。我们得出结论,HUVECs中VCAM-1的表达模式受这些沉默子和NFκB位点的共同控制。