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调节干细胞命运和功能的信号的高通量分析

High-throughput analysis of signals regulating stem cell fate and function.

作者信息

Underhill Gregory H, Bhatia Sangeeta N

机构信息

Harvard-M.I.T. Division of Health Sciences and Technology, Electrical Engineering and Computer Science, Massachusetts Institute of Technology, 77 Massachusetts Ave., E19-502D, Cambridge, MA, USA.

出版信息

Curr Opin Chem Biol. 2007 Aug;11(4):357-66. doi: 10.1016/j.cbpa.2007.05.036. Epub 2007 Jul 25.

Abstract

Stem cells exhibit promise in numerous areas of regenerative medicine. Their fate and function are governed by a combination of intrinsic determinants and signals from the local microenvironment, or niche. An understanding of the mechanisms underlying both embryonic and adult stem cell functions has been greatly enhanced by the recent development of several high-throughput technologies: microfabricated platforms, including cellular microarrays, to investigate the combinatorial effects of microenvironmental stimuli and large-scale screens utilizing small molecules and short interfering RNAs to identify crucial genetic and signaling elements. Furthermore, the integration of these systems with other versatile platforms, such as microfluidics and lentiviral microarrays, will continue to enable the detailed elucidation of stem cell processes, and thus, greatly contribute to the development of stem cell based therapies.

摘要

干细胞在再生医学的众多领域展现出前景。它们的命运和功能由内在决定因素以及来自局部微环境(即生态位)的信号共同调控。近期几种高通量技术的发展极大地增进了我们对胚胎干细胞和成体干细胞功能潜在机制的理解:微制造平台,包括细胞微阵列,用于研究微环境刺激的组合效应;利用小分子和短干扰RNA进行大规模筛选,以识别关键的基因和信号元件。此外,将这些系统与其他多功能平台(如微流体和慢病毒微阵列)相结合,将继续有助于详细阐明干细胞过程,从而极大地推动基于干细胞疗法的发展。

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