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干细胞建模:从基因网络到细胞群体

Stem cell modeling: From gene networks to cell populations.

作者信息

Wu Jincheng, Rostami Mahboubeh Rahmati, Tzanakakis Emmanuel S

机构信息

Department of Chemical and Biological Engineering, State University of New York at Buffalo, Buffalo, NY 14260.

出版信息

Curr Opin Chem Eng. 2013 Feb 1;2(1):17-25. doi: 10.1016/j.coche.2013.01.001.

DOI:10.1016/j.coche.2013.01.001
PMID:23914346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3727911/
Abstract

Despite rapid advances in the field of stem/progenitor cells through experimental studies, relevant modeling approaches have not progressed with a similar pace. Various models have focused on particular aspects of stem cell physiology including gene regulatory networks, gene expression noise and signaling cascades activated by exogenous factors. However, the self-renewal and differentiation of stem cells is driven by the coordinated regulation of events at the subcellular, intercellular and milieu levels. Such events also span multiple time domains from the fast molecular reactions governing gene expression to the slower cell cycle and division. Thus, the development of multiscale computational frameworks for stem cell populations is highly desirable. Multiscale models are expected to aid the design of efficient differentiation strategies and bioprocesses for the generation of therapeutically useful stem cell progeny. Yet, challenges in making these models tractable and pairing those to sufficient experimental data prevent their wide adoption by the stem cell community. Here, we review modeling approaches reported for stem cell populations and associated hurdles.

摘要

尽管通过实验研究,干细胞/祖细胞领域取得了快速进展,但相关的建模方法却没有以类似的速度发展。各种模型都聚焦于干细胞生理学的特定方面,包括基因调控网络、基因表达噪声以及由外源性因素激活的信号级联反应。然而,干细胞的自我更新和分化是由亚细胞、细胞间和环境水平上事件的协同调控驱动的。这些事件还跨越了多个时间域,从控制基因表达的快速分子反应到较慢的细胞周期和分裂。因此,非常需要为干细胞群体开发多尺度计算框架。多尺度模型有望有助于设计高效的分化策略和生物过程,以产生具有治疗用途的干细胞后代。然而,使这些模型易于处理并将其与足够的实验数据配对所面临的挑战,阻碍了它们在干细胞领域的广泛应用。在这里,我们综述了针对干细胞群体报道的建模方法及相关障碍。

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本文引用的文献

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Contribution of stochastic partitioning at human embryonic stem cell division to NANOG heterogeneity.人类胚胎干细胞分裂时的随机分区对 NANOG 异质性的贡献。
PLoS One. 2012;7(11):e50715. doi: 10.1371/journal.pone.0050715. Epub 2012 Nov 30.
2
Stochastic modeling of stem-cell dynamics with control.带有控制的干细胞动力学随机建模。
Math Biosci. 2012 Dec;240(2):231-40. doi: 10.1016/j.mbs.2012.08.004. Epub 2012 Aug 31.
3
Multi-scale modeling of GMP differentiation based on single-cell genealogies.基于单细胞谱系的 GMP 分化的多尺度建模。
Cell Adh Migr. 2014;8(4):349-59. doi: 10.4161/19336918.2014.969990.
4
Increased culture density is linked to decelerated proliferation, prolonged G1 phase, and enhanced propensity for differentiation of self-renewing human pluripotent stem cells.培养密度增加与自我更新的人类多能干细胞增殖减速、G1期延长以及分化倾向增强有关。
Stem Cells Dev. 2015 Apr 1;24(7):892-903. doi: 10.1089/scd.2014.0384. Epub 2014 Dec 22.
FEBS J. 2012 Sep;279(18):3488-500. doi: 10.1111/j.1742-4658.2012.08664.x. Epub 2012 Jul 3.
4
High-throughput approaches for the analysis of extrinsic regulators of stem cell fate.高通量方法分析干细胞命运的外在调节因子。
Curr Opin Cell Biol. 2012 Apr;24(2):236-44. doi: 10.1016/j.ceb.2012.01.006. Epub 2012 Jan 31.
5
Dissecting ensemble networks in ES cell populations reveals micro-heterogeneity underlying pluripotency.剖析胚胎干细胞群体中的集成网络揭示了多能性背后的微观异质性。
Mol Biosyst. 2012 Mar;8(3):744-52. doi: 10.1039/c1mb05398a. Epub 2012 Jan 5.
6
Graded Nodal/Activin signaling titrates conversion of quantitative phospho-Smad2 levels into qualitative embryonic stem cell fate decisions.分级节点/激活素信号调节定量磷酸化 Smad2 水平转化为定性胚胎干细胞命运决定。
PLoS Genet. 2011 Jun;7(6):e1002130. doi: 10.1371/journal.pgen.1002130. Epub 2011 Jun 23.
7
Nanog variability and pluripotency regulation of embryonic stem cells--insights from a mathematical model analysis.Nanog 变异性和胚胎干细胞的多能性调控——来自数学模型分析的见解。
PLoS One. 2010 Jun 21;5(6):e11238. doi: 10.1371/journal.pone.0011238.
8
Regulated fluctuations in nanog expression mediate cell fate decisions in embryonic stem cells.Nanog表达的规律性波动介导胚胎干细胞的细胞命运决定。
PLoS Biol. 2009 Jul;7(7):e1000149. doi: 10.1371/journal.pbio.1000149. Epub 2009 Jul 7.
9
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