Marucci Lucia
Department of Engineering Mathematics, University of Bristol, Bristol BS8 1UB, UK.
BrisSynBio, Life Sciences Building, Tyndall Avenue, Bristol BS8 1TQ, UK.
Stem Cells Int. 2017;2017:7160419. doi: 10.1155/2017/7160419. Epub 2017 Jun 8.
Mouse embryonic stem cells (mESCs), derived from the inner cell mass of the blastocyst, are pluripotent stem cells having self-renewal capability and the potential of differentiating into every cell type under the appropriate culture conditions. An increasing number of reports have been published to uncover the molecular mechanisms that orchestrate pluripotency and cell fate specification using combined computational and experimental methodologies. Here, we review recent systems biology approaches to describe the causes and functions of gene expression heterogeneity and complex temporal dynamics of pluripotency markers in mESCs under uniform culture conditions. In particular, we focus on the dynamics of Nanog, a key regulator of the core pluripotency network and of mESC fate. We summarize the strengths and limitations of different experimental and modeling approaches and discuss how various strategies could be used.
小鼠胚胎干细胞(mESCs)来源于囊胚的内细胞团,是具有自我更新能力的多能干细胞,在适当的培养条件下有分化为各种细胞类型的潜力。越来越多的报告通过结合计算和实验方法,揭示了调控多能性和细胞命运特化的分子机制。在这里,我们回顾了最近的系统生物学方法,以描述在均匀培养条件下mESCs中基因表达异质性和多能性标志物复杂时间动态的原因和功能。特别是,我们关注核心多能性网络和mESC命运的关键调节因子Nanog的动态变化。我们总结了不同实验和建模方法的优缺点,并讨论了如何运用各种策略。