University of California, Department of Chemical Engineering, Berkeley, CA 94720-3220, USA.
IET Syst Biol. 2010 Jan;4(1):1-11. doi: 10.1049/iet-syb.2009.0011.
Stem cells have the capability to self-renew and maintain their undifferentiated state or to differentiate into one or more specialised cell types. Stem cell expansion and manipulation ex vivo is a promising approach for engineering cell replacement therapies, and endogenous stem cells represent potential drugable targets for tissue repair. Before we can harness stem cells' therapeutic potential, we must first understand the intracellular mechanisms controlling their fate choices. These mechanisms involve complex signal transduction and gene regulation networks that feature, for example, intricate feed-forward loops, feedback loops and cross-talk between multiple signalling pathways. Systems biology applies computational and experimental approaches to investigate the emergent behaviour of collections of molecules and strives to explain how these numerous components interact to regulate molecular, cellular and organismal behaviour. Here we review systems biology, and in particular computational, efforts to understand the intracellular mechanisms of stem cell fate choice. We first discuss deterministic and stochastic models that synthesise molecular knowledge into mathematical formalism, enable simulation of important system behaviours and stimulate further experimentation. In addition, statistical analyses such as Bayesian networks and principal components analysis (PCA)/partial least squares (PLS) regression can distill large datasets into more readily managed networks and principal components that provide insights into the critical aspects and components of regulatory networks. Collectively, integrating modelling with experimentation has strong potential for enabling a deeper understanding of stem cell fate choice and thereby aiding the development of therapies to harness stem cells' therapeutic potential.
干细胞具有自我更新和维持未分化状态或分化为一种或多种特化细胞类型的能力。干细胞的体外扩增和操纵是工程细胞替代疗法的一种很有前途的方法,内源性干细胞代表了组织修复的潜在可治疗靶点。在我们能够利用干细胞的治疗潜力之前,我们必须首先了解控制其命运选择的细胞内机制。这些机制涉及复杂的信号转导和基因调控网络,例如,复杂的前馈环、反馈环和多个信号通路之间的串扰。系统生物学应用计算和实验方法来研究分子集合的涌现行为,并努力解释这些众多组件如何相互作用以调节分子、细胞和机体行为。在这里,我们回顾了系统生物学,特别是计算方法,以了解干细胞命运选择的细胞内机制。我们首先讨论了确定性和随机模型,这些模型将分子知识综合成数学形式,能够模拟重要的系统行为并激发进一步的实验。此外,贝叶斯网络和主成分分析(PCA)/偏最小二乘回归(PLS)等统计分析可以将大型数据集提炼成更易于管理的网络和主成分,从而深入了解调控网络的关键方面和组件。总之,将建模与实验相结合具有很大的潜力,可以更深入地了解干细胞命运选择,并有助于开发利用干细胞治疗潜力的疗法。