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首页> 外文期刊>Journal of Cell Science >Netrin-1 regulates invasion and migration of mouse mammary epithelial cells overexpressing Cripto-1 in vitro and in vivo
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Netrin-1 regulates invasion and migration of mouse mammary epithelial cells overexpressing Cripto-1 in vitro and in vivo

机译:Netrin-1在体内外调节过表达Cripto-1的小鼠乳腺上皮细胞的侵袭和迁移

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摘要

The neuronal guidance molecule, Netrin-1, has been suggested to play a role in the adhesion and migration of the mammary gland epithelium. Human and mouse Cripto-1 induce proliferation, migration, invasion and colony formation by epithelial cells in 3D matrices. Here we investigate whether Netrin-1 affects these Cripto-1-dependent activities in mouse mammary epithelial cells. Overexpression of Cripto-1 in EpH4 and HC-11 cells (EpH4/Cripto-1 or HC-11/Cripto-1) was associated with low expression of Netrin-1 and increased expression of its receptor Neogenin compared to that of wild-type cells. No change was observed in the expression of the other Netrin-1 receptor, UNC5H1. Treating EpH4/Cripto-1 or HC-11/Cripto-1 mammary cells with exogenous soluble Netrin-1 resulted in increased expression of E-cadherin and UNC5H1, decreased expression of vimentin and decreased activation of Akt as determined by western blotting. Colony formation by Eph4/Cripto-1 cells in 3D gels was significantly reduced in proximity to a Netrin-1 source, and mammary glands of transgenic mice overexpressing human Cripto-1 showed altered ductal growth in proximity to implanted Netrin-l-releasing pellets. Terminal end buds in the treated transgenic mice mammary glands also showed increased expression of E-cadherin and UNC5H1 and decreased expression of active Akt determined by immunohistochemistry. Together, these results suggest that regulation of Netrin-1 expression is important in regulating Cripto-l-dependent invasion and migration of mammary epithelial cells.
机译:已建议神经元指导分子Netrin-1在乳腺上皮的粘附和迁移中发挥作用。人类和小鼠Cripto-1通过3D基质中的上皮细胞诱导增殖,迁移,侵袭和集落形成。在这里,我们调查Netrin-1是否会影响小鼠乳腺上皮细胞中的这些Cripto-1依赖性活动。与野生型相比,Eph4和HC-11细胞(EpH4 / Cripto-1或HC-11 / Cripto-1)中Cripto-1的过表达与Netrin-1的低表达及其受体Neogenin的表达增加有关。细胞。其他Netrin-1受体UNC5H1的表达未见变化。用Western印迹测定,用外源可溶性Netrin-1处理EpH4 / Cripto-1或HC-11 / Cripto-1乳腺细胞会导致E-钙黏着蛋白和UNC5H1的表达增加,波形蛋白的表达减少以及Akt的激活降低。在Netrin-1来源附近,Eph4 / Cripto-1细胞在3D凝胶中的集落形成显着减少,过表达人类Cripto-1的转基因小鼠的乳腺在植入Netrin-1释放颗粒附近显示出导管生长改变。经处理的转基因小鼠乳腺的末端芽也显示出通过免疫组织化学确定的E-钙粘着蛋白和UNC5H1的表达增加,而活性Akt的表达减少。总之,这些结果表明,调节Netrin-1表达在调节Cripto-l依赖性乳腺上皮细胞的侵袭和迁移中很重要。

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