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Spatial Pattern Dynamics of 3D Stem Cell Loss of Pluripotency via Rules-Based Computational Modeling

机译:通过基于规则的计算建模的3D干细胞多能性的空间格局动力学

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Pluripotent embryonic stem cells (ESCs) have the unique ability to differentiate into cells from all germ lineages, making them a potentially robust cell source for regenerative medicine therapies, but difficulties in predicting and controlling ESC differentiation currently limit the development of therapies and applications from such cells. A common approach to induce the differentiation of ESCs in vitro is via the formation of multicellular aggregates known as embryoid bodies (EBs), yet cell fate specification within EBs is generally considered an ill-defined and poorly controlled process. Thus, the objective of this study was to use rules-based cellular modeling to provide insight into which processes influence initial cell fate transitions in 3-dimensional microenvironments. Mouse embryonic stem cells (D3 cell line) were differentiated to examine the temporal and spatial patterns associated with loss of pluripotency as measured through Oct4 expression. Global properties of the multicellular aggregates were accurately recapitulated by a physics-based aggregation simulation when compared to experimentally measured physical parameters of EBs. Oct4 expression patterns were analyzed by confocal microscopy over time and compared to simulated trajectories of EB patterns. The simulations demonstrated that loss of Oct4 can be modeled as a binary process, and that associated patterns can be explained by a set of simple rules that combine baseline stochasticity with intercellular communication. Competing influences between Oct4+ and Oct4? neighbors result in the observed patterns of pluripotency loss within EBs, establishing the utility of rules-based modeling for hypothesis generation of underlying ESC differentiation processes. Importantly, the results indicate that the rules dominate the emergence of patterns independent of EB structure, size, or cell division. In combination with strategies to engineer cellular microenvironments, this type of modeling approach is a powerful tool to predict stem cell behavior under a number of culture conditions that emulate characteristics of 3D stem cell niches.
机译:多能胚胎干细胞(ESC)具有从所有细菌谱系分化为细胞的独特能力,使其成为再生医学疗法的潜在强大细胞来源,但是目前预测和控制ESC分化的困难限制了这种疗法的开发和应用细胞。体外诱导ESC分化的一种常用方法是通过形成称为胚状体(EBs)的多细胞聚集体,但是EB中的细胞命运规范通常被认为是定义不明确且控制不佳的过程。因此,本研究的目的是使用基于规则的细胞模型来深入了解哪些过程会影响3维微环境中的初始细胞命运转变。小鼠胚胎干细胞(D3细胞系)进行了分化,以检查与通过Oct4表达测量的多能性丧失相关的时间和空间模式。与实验测量的EB物理参数相比,通过基于物理的聚集模拟可以准确地概括多细胞聚集体的全局特性。通过共聚焦显微镜对Oct4表达模式进行了分析,并将其与EB模式的模拟轨迹进行了比较。仿真表明,Oct4的损失可以建模为一个二进制过程,并且可以通过将基线随机性与细胞间通讯结合在一起的一组简单规则来解释相关模式。 Oct4 +和Oct4之间的竞争影响?邻居导致在EB中观察到的多能性损失模式,从而建立了基于规则的建模实用程序,用于潜在的ESC分化过程的假设生成。重要的是,结果表明该规则支配了与EB结构,大小或细胞分裂无关的模式的出现。结合工程化细胞微环境的策略,这种类型的建模方法是一种强大的工具,可以在模拟3D干细胞生态位特征的多种培养条件下预测干细胞行为。

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