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狨猴和人类滋养层干细胞在信号需求上存在差异,并再现了不同的滋养层侵袭模式。

Marmoset and human trophoblast stem cells differ in signaling requirements and recapitulate divergent modes of trophoblast invasion.

机构信息

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK; Wellcome Trust, Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, UK.

Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK; Wellcome Trust, Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, UK; Department of Biochemistry, University of Cambridge, Cambridge, UK.

出版信息

Cell Stem Cell. 2024 Oct 3;31(10):1427-1446.e8. doi: 10.1016/j.stem.2024.09.004. Epub 2024 Sep 24.

Abstract

Early human trophoblast development has remained elusive due to the inaccessibility of the early conceptus. Non-human primate models recapitulate many features of human development and allow access to early postimplantation stages. Here, we tracked the pre- to postimplantation transition of the trophoblast lineage in superficially implanting marmoset embryos in vivo. We differentiated marmoset naive pluripotent stem cells into trophoblast stem cells (TSCs), which exhibited trophoblast-specific transcriptome, methylome, differentiation potential, and long-term self-renewal. Notably, human TSC culture conditions failed to support marmoset TSC derivation, instead inducing an extraembryonic mesoderm-like fate in marmoset cells. We show that combined MEK, TGF-β/NODAL, and histone deacetylase inhibition stabilizes a periimplantation trophoblast-like identity in marmoset TSCs. By contrast, these conditions differentiated human TSCs toward extravillous trophoblasts. Our work presents a paradigm to harness the evolutionary divergence in implantation strategies to elucidate human trophoblast development and invasion.

摘要

由于早期胚胎无法接近,早期人类滋养层的发育一直难以捉摸。非人类灵长类动物模型再现了许多人类发育的特征,并允许进入早期植入后阶段。在这里,我们在体内跟踪了表面植入的狨猴胚胎中滋养层谱系的植入前到植入后的转变。我们将狨猴幼稚多能干细胞分化为滋养层干细胞(TSC),这些细胞表现出滋养层特异性的转录组、甲基组、分化潜能和长期自我更新。值得注意的是,人类 TSC 培养条件不能支持狨猴 TSC 的衍生,而是在狨猴细胞中诱导出胚外中胚层样命运。我们表明,MEK、TGF-β/NODAL 和组蛋白去乙酰化酶的联合抑制稳定了狨猴 TSC 中植入后滋养层样的特征。相比之下,这些条件使人类 TSC 向绒毛外滋养层分化。我们的工作提出了一个范例,利用植入策略的进化分歧来阐明人类滋养层的发育和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f0/7616712/a72bcc06d7ba/EMS199345-f008.jpg

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