Gory S, Vernet M, Laurent M, Dejana E, Dalmon J, Huber P
Commissariat à l'Energie Atomique (CEA), Laboratoire de Transgenèse et Différenciation Cellulaire, Département de Biologie Moléculaire et Structurale, Grenoble, France.
Blood. 1999 Jan 1;93(1):184-92.
Vascular endothelial-cadherin (VE-cadherin) is a calcium-dependent adhesive molecule, exclusively and constitutively expressed in endothelial cells. Analysis of the VE-cadherin promoter fused to a reporter gene in bovine aortic endothelial cells showed three major functional regions. The proximal region alone (-139, +24) promoted nonspecific transcription; the addition of the (-289, -140) and (-2226, -1190) domains abolished transcription in fibroblasts while expression in endothelial cells remained unchanged, suggesting that fragments (-2226, +24) and longer contain the full endogenous promoter activity. To study the transcriptional specificity of the promoter region in vivo, we generated transgenic mice carrying the chimeric construct containing the (-2486, +24) region. The promoter directed reporter expression in all examined organs of adult transgenic mice. During embryonic development, transgene expression was detected at the early steps of vasculogenesis. Later, the expression persisted during development of the vascular system and was restricted to the endothelial layer of the vessels. Together, these data provide evidence for specific regulatory regions within the VE-cadherin promoter. Furthermore, the identification of DNA sequences restricting gene expression to the endothelium has many potential applications for the development of animal models of cardiovascular or angiogenic diseases or for the delivery of therapeutic molecules.
血管内皮钙黏蛋白(VE-钙黏蛋白)是一种钙依赖性黏附分子,仅在内皮细胞中组成性表达。对与报告基因融合的VE-钙黏蛋白启动子在牛主动脉内皮细胞中的分析显示出三个主要功能区域。仅近端区域(-139,+24)促进非特异性转录;添加(-289,-140)和(-2226,-1190)结构域可消除成纤维细胞中的转录,而在内皮细胞中的表达保持不变,这表明片段(-2226,+24)及更长片段包含完整的内源性启动子活性。为了研究体内启动子区域的转录特异性,我们构建了携带包含(-2486,+24)区域的嵌合构建体的转基因小鼠。该启动子指导成年转基因小鼠所有检测器官中的报告基因表达。在胚胎发育过程中,在血管生成的早期阶段检测到转基因表达。后来,在血管系统发育过程中该表达持续存在,并局限于血管的内皮细胞层。总之,这些数据为VE-钙黏蛋白启动子内的特定调控区域提供了证据。此外,将基因表达限制在内皮细胞的DNA序列的鉴定对于心血管或血管生成性疾病动物模型的开发或治疗分子的递送具有许多潜在应用。