Ponticos Markella, Partridge Terrence, Black Carol M, Abraham David J, Bou-Gharios George
Centre for Rheumatology, Department of Medicine, University College of London, United Kingdom.
Mol Cell Biol. 2004 Jul;24(14):6151-61. doi: 10.1128/MCB.24.14.6151-6161.2004.
A major component of the vessel wall of large arteries and veins is the extracellular matrix (ECM), which consists of collagens, elastin, and proteoglycans. Collagen type I is one of the most abundant of the ECM proteins. We have previously shown that the pro-collagen type I alpha 2 gene contains an enhancer which confers tissue-specific expression in the majority of collagen-producing cells, including blood vessels. In this paper, we delineate a specific vascular smooth muscle cell (vSMC) element: a 100-bp sequence around -16.6 kb upstream of the transcription start site that regulates collagen expression exclusively in vSMCs. Furthermore, we show that the expression is activated through the binding of the homeodomain protein Nkx2.5, which is further potentiated in the presence of GATA6. In contrast, this element was repressed by the binding of the zinc-finger protein deltaEF1/ZEB1. We propose a model of regulation where the activating transcription factor Nkx2.5 and the repressor deltaEF1/ZEB1 compete for an overlapping DNA binding site. This element is important in understanding the molecular mechanisms of vessel remodeling and is a potential target for intervention in vascular diseases where there is excessive deposition of collagen in the vessel wall.
大动脉和静脉血管壁的一个主要成分是细胞外基质(ECM),它由胶原蛋白、弹性蛋白和蛋白聚糖组成。I型胶原蛋白是ECM蛋白中含量最丰富的一种。我们之前已经表明,I型前胶原α2基因含有一个增强子,该增强子在大多数产生胶原蛋白的细胞(包括血管细胞)中赋予组织特异性表达。在本文中,我们描绘了一个特定的血管平滑肌细胞(vSMC)元件:转录起始位点上游约-16.6 kb处的一个100 bp序列,它仅在vSMC中调节胶原蛋白的表达。此外,我们表明该表达通过同源结构域蛋白Nkx2.5的结合而被激活,在GATA6存在的情况下进一步增强。相反,该元件被锌指蛋白deltaEF1/ZEB1的结合所抑制。我们提出了一种调控模型,其中激活转录因子Nkx2.5和阻遏物deltaEF1/ZEB1竞争一个重叠的DNA结合位点。该元件对于理解血管重塑的分子机制很重要,并且是干预血管壁中胶原蛋白过度沉积的血管疾病的潜在靶点。