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A Resource for the Transcriptional Signature of Bona Fide Trophoblast Stem Cells and Analysis of Their Embryonic Persistence

机译:Bona Fide滋养细胞干细胞转录签名的资源及其胚胎持久性分析

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Trophoblast stem cells (TSCs) represent the multipotent progenitors that give rise to the different cells of the embryonic portion of the placenta. Here, we analysed the expression of key TSC transcription factors Cdx2, Eomes, and Elf5 in the early developing placenta of mouse embryos and in cultured TSCs and reveal surprising heterogeneity in protein levels. We analysed persistence of TSCs in the early placenta and find that TSCs remain in the chorionic hinge until E9.5 and are lost shortly afterwards. To define the transcriptional signature of bona fide TSCs, we used inducible gain- and loss-of-function alleles of Eomes or Cdx2, and Eomes(GFP), to manipulate and monitor the core maintenance factors of TSCs, followed by genome-wide expression profiling. Combinatorial analysis of resulting expression profiles allowed for defining novel TSC marker genes that might functionally contribute to the maintenance of the TSC state. Analyses by qRT-PCR and in situ hybridisation validated novel TSC- and chorion-specific marker genes, such as Bok/Mtd, Cldn26, Duox2, Duoxa2, Nr0b1, and Sox21. Thus, these expression data provide a valuable resource for the transcriptional signature of bona fide and early differentiating TSCs and may contribute to an increased understanding of the transcriptional circuitries that maintain and/or establish stemness of TSCs.
机译:滋养细胞干细胞(TSCs)代表多能祖细胞,其产生胎盘的胚胎部分的不同细胞。在这里,我们分析了小鼠胚胎早期胎盘和培养的TSC中的关键TSC转录因子CDX2,eomes和ELF5的表达,并揭示了蛋白质水平的令人惊讶的异质性。我们在早期胎盘中分析了TSCs的持续性,发现TSCs留在绒毛膜铰链中,直至E9.5,并在后续损失。要定义真正的TSC的转录签名,我们使用了欧姆斯或CDX2的诱导型损失和函数丧失,以及eomes(GFP)来操纵和监控TSC的核心维护因子,其次是基因组的表达分析。所得到的表达型谱的组合分析允许定义可能在能够维持TSC状态的新型TSC标记基因。通过QRT-PCR和原位杂交验证的新型TSC和绒毛膜特异性标记基因分析,例如Bok / MTD,CLDN26,Duox2,DuoxA2,NR0B1和Sox21。因此,这些表达数据提供了对BONA FIDE的转录签名和早期区分TSC的有价值的资源,并且可能有助于提高维持和/或建立TSCs茎的转录电路的了解。

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