Stumpf Patrick S, MacArthur Ben D
Centre for Human Development, Stem Cells and Regeneration, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Front Genet. 2019 Jan 22;10:2. doi: 10.3389/fgene.2019.00002. eCollection 2019.
The molecular regulatory network underlying stem cell pluripotency has been intensively studied, and we now have a reliable ensemble model for the "average" pluripotent cell. However, evidence of significant cell-to-cell variability suggests that the activity of this network varies within individual stem cells, leading to differential processing of environmental signals and variability in cell fates. Here, we adapt a method originally designed for face recognition to infer regulatory network patterns within individual cells from single-cell expression data. Using this method we identify three distinct network configurations in cultured mouse embryonic stem cells-corresponding to naïve and formative pluripotent states and an early primitive endoderm state-and associate these configurations with particular combinations of regulatory network activity archetypes that govern different aspects of the cell's response to environmental stimuli, cell cycle status and core information processing circuitry. These results show how variability in cell identities arise naturally from alterations in underlying regulatory network dynamics and demonstrate how methods from machine learning may be used to better understand single cell biology, and the collective dynamics of cell communities.
干细胞多能性的分子调控网络已得到深入研究,目前我们有一个针对“平均”多能细胞的可靠整体模型。然而,显著的细胞间变异性证据表明,该网络的活性在单个干细胞内存在差异,导致对环境信号的处理不同以及细胞命运的变异性。在这里,我们采用一种最初设计用于人脸识别的方法,从单细胞表达数据推断单个细胞内的调控网络模式。使用这种方法,我们在培养的小鼠胚胎干细胞中识别出三种不同的网络配置——对应于原始和形成性多能状态以及早期原始内胚层状态——并将这些配置与调控网络活动原型的特定组合相关联,这些原型控制细胞对环境刺激、细胞周期状态和核心信息处理电路不同方面的反应。这些结果表明细胞身份的变异性是如何从潜在调控网络动态的改变中自然产生的,并展示了机器学习方法如何用于更好地理解单细胞生物学以及细胞群落的集体动态。