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Snail1、Snail2 和 E47 促进乳腺上皮分支形态发生。

Snail1, Snail2, and E47 promote mammary epithelial branching morphogenesis.

机构信息

Departments of Chemical & Biological Engineering and Molecular Biology, Princeton University, Princeton, NJ, USA.

出版信息

EMBO J. 2011 May 24;30(13):2662-74. doi: 10.1038/emboj.2011.159.

Abstract

Several E-box-binding transcription factors regulate individual and collective cell migration and enhance the motility of epithelial cells by promoting epithelial-mesenchymal transition (EMT). Here, we characterized the role of a subset of these transcription factors and the EMT proteome in branching morphogenesis of mammary epithelial tissues using a three-dimensional organotypic culture model of the mammary duct. We found that the transcription factors Snail1, Snail2, and E47 were transiently upregulated at branch sites; decreasing the expression of these transcription factors inhibited branching. Conversely, ectopic expression of Snail1, Snail2, and E47 induced branching in the absence of exogenous stimuli. These changes correlated with the expression of mesenchymal markers and repression of E-cadherin, which was essential for branching. Snail1 and Snail2 also promoted cell survival at branch sites, but this was not sufficient to induce branching. These findings indicate that Snail1, Snail2, and E47 can promote collective migration during branching morphogenesis of mammary epithelial tissues through key regulators of EMT.

摘要

几个 E 盒结合转录因子通过促进上皮-间充质转化(EMT)来调节细胞的个体和集体迁移,并增强上皮细胞的迁移能力。在这里,我们使用乳腺导管的三维器官培养模型,研究了这些转录因子和 EMT 蛋白质组在乳腺上皮组织的分支形态发生中的作用。我们发现,转录因子 Snail1、Snail2 和 E47 在分支位点上短暂上调;降低这些转录因子的表达会抑制分支。相反,Snail1、Snail2 和 E47 的异位表达在没有外源刺激的情况下诱导分支。这些变化与间充质标志物的表达和 E-钙黏蛋白的抑制相关,E-钙黏蛋白对分支至关重要。Snail1 和 Snail2 还促进了分支部位的细胞存活,但这不足以诱导分支。这些发现表明,Snail1、Snail2 和 E47 可以通过 EMT 的关键调节剂在乳腺上皮组织的分支形态发生中促进集体迁移。

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