Vascular Endothelial Growth Factor Increases Endothelial Nitric Oxide Synthase Transcription In Huvec Cells.

E. Koai, Tibisay Beatriz Rincon Rios, John Edwards
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引用次数: 3

Abstract

Although it is known that VEGF increases eNOS protein, the mechanisms responsible remain unclear. To determine if VEGF alters eNOS transcription, human umbilical vein endothelial cells were transfected with reporters under the control of the eNOS promoter and stimulated with VEGF165. VEGF significantly increased eNOS-mRNA after 2 hours exposure. VEGF significantly increased eNOS reporter activity as early as one hour (268±32%), but this increase returned to baseline after 6 hours. Using deletion constructs, the VEGF response region was initially localized to within the -722/-494 region. GMSA indicated that VEGF increased DNA binding to both a cAMP-like and AP1-like response elements. Site-specific mutations and heterologous constructs indicated that the site centered at AP1-like site was both necessary and sufficient to meditate VEGF transcriptional activation. These results indicate that VEGF rapidly activates eNOS transcription prior to a rise eNOS-mRNA, an effect mediated by a cis-trans interaction localized to an AP1-like site within the eNOS promoter.
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血管内皮生长因子增加Huvec细胞内皮型一氧化氮合酶转录。
虽然已知VEGF增加eNOS蛋白,但其机制尚不清楚。为了确定VEGF是否会改变eNOS的转录,在eNOS启动子的控制下,用报告基因转染人脐静脉内皮细胞,并用VEGF165刺激。VEGF在暴露2小时后显著增加eNOS-mRNA。VEGF可显著提高eNOS报告细胞活性(268±32%),但6小时后恢复到基线水平。使用删除结构,VEGF反应区域最初定位于-722/-494区域内。GMSA表明VEGF增加了DNA与camp样和ap1样反应元件的结合。位点特异性突变和异源构建表明,以ap1样位点为中心的位点是抑制VEGF转录激活的必要和充分条件。这些结果表明,VEGF在eNOS- mrna升高之前迅速激活eNOS转录,这一作用是由eNOS启动子内ap1样位点的顺式-反式相互作用介导的。
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