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The metabolic network model of primedaive human embryonic stem cells underlines the importance of oxidation-reduction potential and tryptophan metabolism in primed pluripotency

机译:已启动/未启动的人类胚胎干细胞的代谢网络模型强调了在启动多能性中氧化还原电位和色氨酸代谢的重要性

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摘要

BackgroundPluripotency is proposed to exist in two different stages: Naive and Primed. Conventional human pluripotent cells are essentially in the primed stage. In recent years, several protocols have claimed to generate naive human embryonic stem cells (hESCs). To the best of our knowledge, none of these protocols is currently recognized as the gold standard method. Furthermore, the consistency of the resulting cells from these diverse protocols at the molecular level is yet to be shown. Additionally, little is known about the principles that govern the metabolic differences between naive and primed pluripotency. In this work, using a computational approach, we tried to shed light on these basic issues.
机译:背景建议多能性存在于两个不同的阶段:天真和素色。常规的人类多能细胞基本上处于启动阶段。近年来,一些协议声称可以生成幼稚的人类胚胎干细胞(hESC)。据我们所知,这些协议目前都不被认为是黄金标准方法。此外,由这些不同方案产生的细胞在分子水平上的一致性尚待显示。另外,对于控制幼稚多能性和致敏多能性之间的代谢差异的原理知之甚少。在这项工作中,我们使用一种计算方法,试图阐明这些基本问题。

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