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短尾蛋白与Wnt/β-连环蛋白信号通路协同作用,在分化的小鼠胚胎干细胞中引发原始条纹样行为。

Brachyury cooperates with Wnt/β-catenin signalling to elicit primitive-streak-like behaviour in differentiating mouse embryonic stem cells.

作者信息

Turner David A, Rué Pau, Mackenzie Jonathan P, Davies Eleanor, Martinez Arias Alfonso

出版信息

BMC Biol. 2014 Aug 13;12:63. doi: 10.1186/s12915-014-0063-7.

Abstract

BACKGROUND

The formation of the primitive streak is the first visible sign of gastrulation, the process by which the three germ layers are formed from a single epithelium during early development. Embryonic stem cells (ESCs) provide a good system for understanding the molecular and cellular events associated with these processes. Previous work, both in embryos and in culture, has shown how converging signals from both nodal/TGFβR and Wnt/β-catenin signalling pathways specify cells to adopt a primitive-streak-like fate and direct them to undertake an epithelial-to-mesenchymal transition (EMT). However, many of these approaches have relied on genetic analyses without taking into account the temporal progression of events within single cells. In addition, it is still unclear to what extent events in the embryo are able to be reproduced in culture.

RESULTS

Here, we combine flow cytometry and a quantitative live single-cell imaging approach to demonstrate how the controlled differentiation of mouse ESCs towards a primitive streak fate in culture results in cells displaying many of the characteristics observed during early mouse development including transient brachyury expression, EMT and increased motility. We also find that the EMT initiates the process, and this is both fuelled and terminated by the action of brachyury, whose expression is dependent on the EMT and β-catenin activity.

CONCLUSIONS

As a consequence of our analysis, we propose that a major output of brachyury expression is in controlling the velocity of the cells that are transiting out of the primitive streak.

摘要

背景

原条的形成是原肠胚形成的首个可见标志,原肠胚形成是在早期发育过程中由单一上皮细胞形成三个胚层的过程。胚胎干细胞(ESC)为理解与这些过程相关的分子和细胞事件提供了一个良好的系统。先前在胚胎和培养物中的研究工作已经表明,来自节点/TGFβR和Wnt/β-连环蛋白信号通路的汇聚信号如何使细胞获得类似原条的命运,并引导它们进行上皮-间充质转化(EMT)。然而,许多这些方法依赖于基因分析,而没有考虑单个细胞内事件的时间进程。此外,目前仍不清楚胚胎中的事件在培养物中能够在多大程度上得以重现。

结果

在此,我们结合流式细胞术和定量实时单细胞成像方法,以证明在培养物中小鼠胚胎干细胞向原条命运的受控分化如何导致细胞表现出许多在小鼠早期发育过程中观察到的特征,包括短暂的短尾相关蛋白表达、上皮-间充质转化和运动性增加。我们还发现上皮-间充质转化启动了这一过程,并且这一过程由短尾相关蛋白的作用推动并终止,其表达依赖于上皮-间充质转化和β-连环蛋白活性。

结论

作为我们分析的结果,我们提出短尾相关蛋白表达的一个主要作用是控制从原条中转出的细胞的速度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b5a/4171571/893309d75ae8/12915_2014_63_Fig1_HTML.jpg

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