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The Hippo Pathway Effector YAP1 Regulates Intestinal Epithelial Cell Differentiation

机译:Hippo途径效应器YAP1调节肠上皮细胞分化

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摘要

The human intestine is covered by epithelium, which is continuously replaced by new cells provided by stem cells located at the bottom of the glands. The maintenance of intestinal stem cells is supported by a niche which is composed of several signaling proteins including the Hippo pathway effectors YAP1/TAZ. The role of YAP1/TAZ in cell proliferation and regeneration is well documented but their involvement on the differentiation of intestinal epithelial cells is unclear. In the present study, the role of YAP1/TAZ on the differentiation of intestinal epithelial cells was investigated using the HT29 cell line, the only multipotent intestinal cell line available, with a combination of knockdown approaches. The expression of intestinal differentiation cell markers was tested by qPCR, Western blot, indirect immunofluorescence and electron microscopy analyses. The results show that TAZ is not expressed while the abolition of YAP1 expression led to a sharp increase in goblet and absorptive cell differentiation and reduction of some stem cell markers. Further studies using double knockdown experiments revealed that most of these effects resulting from YAP1 abolition are mediated by CDX2, a key intestinal cell transcription factor. In conclusion, our results indicate that YAP1/TAZ negatively regulate the differentiation of intestinal epithelial cells through the inhibition of CDX2 expression.
机译:人肠由上皮覆盖,上皮覆盖,其连续被位于腺体底部的干细胞提供的新细胞替换。肠干细胞的维持由含有肝脏途径的若干信号蛋白组成,包括河马途径YAP1 / TAZ。 YAP1 / TAZ在细胞增殖和再生中的作用良好记录,但它们对肠上皮细胞的分化的参与尚不清楚。在本研究中,使用HT29细胞系,研究了YAP1 / TAZ对肠上皮细胞分化的作用,唯一可用的多能肠道细胞系,具有敲低方法。通过QPCR,Western印迹,间接免疫荧光和电子显微镜分析测试肠道分化细胞标记物的表达。结果表明,在取消YAP1表达导致高脚瓣和吸收细胞分化的急剧增加和一些干细胞标记的情况下,TAZ不会表达。使用双敲低实验的进一步研究表明,由YAP1废除产生的大多数效应由CDX2介导的关键肠细胞转录因子。总之,我们的结果表明,YAP1 / TAZ通过抑制CDX2表达来对肠上皮细胞的分化产生负面调节。

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