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Molecular Criteria for Defining the Naive Human Pluripotent State

机译:定义幼稚人多能状态的分子标准

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SUMMARY Recent studies have aimed to convert cultured human pluripotent cells to a naive state, but it remains unclear to what extent the resulting cells recapitulate in vivo naive pluripotency. Here we propose a set of molecular criteria for evaluating the naive human pluripotent state by comparing it to the human embryo. We show that transcription of transposable elements provides a sensitive measure of the concordance between pluripotent stem cells and early human development. We also show that induction of the naive state is accompanied by genome-wide DNA hypomethylation, which is reversible except at imprinted genes, and that the X chromosome status resembles that of the human preimplantation embryo. However, we did not see efficient incorporation of naive human cells into mouse embryos. Overall, the different naive conditions we tested showed varied relationships to human embryonic states based on molecular criteria, providing a backdrop for future analysis of naive human pluripotency.
机译:发明内容最近的研究旨在将培养的人多能细胞转化为幼稚状态,但仍然尚不清楚所得细胞在体内幼稚多能性中概括的程度。在这里,我们提出了一系列的分子标准,用于通过将其与人胚胎进行比较来评估幼稚人多能状态。我们表明转移元素的转录提供多能干细胞和早期人类发展之间的一致性的敏感措施。我们还表明,幼稚状态的诱导伴随着基因组 - 宽DNA低甲基化,除了印迹基因外是可逆的,并且X染色体状态类似于人类预体胚胎。然而,我们没有看到将幼稚人细胞有效地结合到小鼠胚胎中。总体而言,我们测试的不同Naive病症基于分子标准显示与人胚胎状态的变化关系,为未来的幼稚人多能性分析进行了背景。

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