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Mechanisms of trophectoderm fate specification in preimplantation mouse development

机译:滋养外胚层命运规范在植入前小鼠发育中的机制

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摘要

During preimplantation mouse development, embryos establish two distinct cell lineages by the time of blastocyst formation: trophectoderm (TE) and inner cell mass (ICM). To explain the mechanism of this cell fate specification, two classical models, namely the inside-outside model and polarity model have been proposed based on experimental manipulation studies on embryos. This review summarizes recent findings on the molecular mechanisms of fate specification, and discusses how these findings fit into the classical models. TE development is regulated by a transcription factor cascade, the core transcription factors of which are Tead4 and Cdx2. The transcriptional activity of Tead4 is regulated by the position-dependent Hippo signaling pathway, thus supporting the inside-outside model. In contrast, several findings support the polarity model; some other findings suggest different mechanisms. We also discuss how the two classical models could be further developed in the light of recent molecular findings.
机译:在植入前小鼠的发育过程中,胚在胚泡形成时会建立两个不同的细胞谱系:滋养外胚层(TE)和内部细胞团(ICM)。为了解释该细胞命运规范的机制,基于对胚胎的实验操作研究,提出了两个经典模型,即内-外模型和极性模型。这篇综述总结了关于命运规范分子机制的最新发现,并讨论了这些发现如何适合经典模型。 TE的发育受转录因子级联的调节,其核心转录因子为Tead4和Cdx2。 Tead4的转录活性受位置依赖的Hippo信号通路调节,从而支持内外模型。相反,一些发现支持极性模型。其他一些发现提示了不同的机制。我们还将讨论如何根据最近的分子发现进一步开发这两种经典模型。

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