Niessen Kyle, Fu YangXin, Chang Linda, Hoodless Pamela A, McFadden Deborah, Karsan Aly
Department of Medical Biophysics, British Columbia Cancer Agency, Vancouver V5Z 1L3, Canada.
J Cell Biol. 2008 Jul 28;182(2):315-25. doi: 10.1083/jcb.200710067.
Snail family proteins are key regulators of epithelial-mesenchymal transition, but their role in endothelial-to-mesenchymal transition (EMT) is less well studied. We show that Slug, a Snail family member, is expressed by a subset of endothelial cells as well as mesenchymal cells of the atrioventricular canal and outflow tract during cardiac cushion morphogenesis. Slug deficiency results in impaired cellularization of the cardiac cushion at embryonic day (E)-9.5 but is compensated by increased Snail expression at E10.5, which restores cardiac cushion EMT. We further demonstrate that Slug, but not Snail, is directly up-regulated by Notch in endothelial cells and that Slug expression is required for Notch-mediated repression of the vascular endothelial cadherin promoter and for promoting migration of transformed endothelial cells. In contrast, transforming growth factor beta (TGF-beta) induces Snail but not Slug. Interestingly, activation of Notch in the context of TGF-beta stimulation results in synergistic up-regulation of Snail in endothelial cells. Collectively, our data suggest that combined expression of Slug and Snail is required for EMT in cardiac cushion morphogenesis.
蜗牛家族蛋白是上皮-间充质转化的关键调节因子,但其在内皮-间充质转化(EMT)中的作用研究较少。我们发现,蜗牛家族成员蛞蝓蛋白(Slug)在心脏垫形态发生过程中,由一部分内皮细胞以及房室管和流出道的间充质细胞表达。Slug缺陷导致胚胎期(E)-9.5时心脏垫的细胞化受损,但在E10.5时通过增加蜗牛蛋白(Snail)的表达得到补偿,从而恢复心脏垫EMT。我们进一步证明,在内皮细胞中,Notch直接上调Slug而非Snail,并且Slug表达是Notch介导的血管内皮钙黏蛋白启动子抑制以及促进转化内皮细胞迁移所必需的。相反,转化生长因子β(TGF-β)诱导Snail而非Slug。有趣的是,在TGF-β刺激的背景下激活Notch会导致内皮细胞中Snail的协同上调。总体而言,我们的数据表明,Slug和Snail的联合表达是心脏垫形态发生中EMT所必需的。