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通过单细胞基因表达分析对人类囊胚进行时空重建,为诱导原始多能性提供信息。

Spatiotemporal Reconstruction of the Human Blastocyst by Single-Cell Gene-Expression Analysis Informs Induction of Naive Pluripotency.

机构信息

Department of Obstetrics and Gynecology, Stanford University, Stanford, CA 94305, USA; Institute for Stem Cell Biology & Regenerative Medicine, Stanford University, Stanford, CA 94305, USA.

Department of Obstetrics and Gynecology, Stanford University, Stanford, CA 94305, USA; Institute for Stem Cell Biology & Regenerative Medicine, Stanford University, Stanford, CA 94305, USA; Department of Genetics, Institute for Stem Cell Biology & Regenerative Medicine, Stanford University, Stanford, CA 94305, USA.

出版信息

Dev Cell. 2016 Jul 11;38(1):100-15. doi: 10.1016/j.devcel.2016.06.014.

Abstract

Human preimplantation embryo development involves complex cellular and molecular events that lead to the establishment of three cell lineages in the blastocyst: trophectoderm, primitive endoderm, and epiblast. Owing to limited resources of biological specimens, our understanding of how the earliest lineage commitments are regulated remains narrow. Here, we examined gene expression in 241 individual cells from early and late human blastocysts to delineate dynamic gene-expression changes. We distinguished all three lineages and further developed a 3D model of the inner cell mass and trophectoderm in which individual cells were mapped into distinct expression domains. We identified in silico precursors of the epiblast and primitive endoderm lineages and revealed a role for MCRS1, TET1, and THAP11 in epiblast formation and their ability to induce naive pluripotency in vitro. Our results highlight the potential of single-cell gene-expression analysis in human preimplantation development to instruct human stem cell biology.

摘要

人类胚胎着床前的发育涉及复杂的细胞和分子事件,这些事件导致囊胚中三个细胞谱系的建立:滋养外胚层、原始内胚层和上胚层。由于生物样本资源有限,我们对最早的谱系决定因素如何受到调控的认识仍然很有限。在这里,我们检查了来自早期和晚期人类囊胚的 241 个单个细胞中的基因表达,以描绘动态的基因表达变化。我们区分了所有三个谱系,并进一步开发了内细胞团和滋养外胚层的 3D 模型,其中将单个细胞映射到不同的表达域中。我们在计算机上鉴定了上胚层和原始内胚层谱系的前体,并揭示了 MCRS1、TET1 和 THAP11 在胚胎形成中的作用,以及它们在体外诱导原始多能性的能力。我们的研究结果强调了单细胞基因表达分析在人类胚胎着床前发育中的潜力,以指导人类干细胞生物学。

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