Arrayed cellular microenvironments for identifying culture and differentiation conditions for stem, primary and rare cell populations

被引:45
|
作者
Brafman, David A. [1 ]
Chien, Shu [2 ]
Willert, Karl [1 ]
机构
[1] Univ Calif San Diego, Stem Cell Program, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Dept Bioengn, San Diego, CA 92103 USA
关键词
THROUGHPUT SCREENING DATA; COMBINATORIAL MICROENVIRONMENTS; EXTRACELLULAR ENVIRONMENT; CLUSTER-ANALYSIS; MICROARRAY DATA; PROTEINS; SURVIVAL; PRODUCTS; FATE; CHIP;
D O I
10.1038/nprot.2012.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During the development of an organism, cells are exposed to a myriad of signals, structural components and scaffolds, which collectively make up the cellular microenvironment. The majority of current developmental biology studies examine the effect of individual or small subsets of molecules and parameters on cellular behavior, and they consequently fail to explore the complexity of factors to which cells are exposed. Here we describe a technology, referred to as arrayed cellular microenvironments (ACMEs), that allows for a high-throughput examination of the effects of multiple extracellular components in a combinatorial manner on any cell type of interest. We will specifically focus on the application of this technology to human pluripotent stem cells (hPSCs), a population of cells with tremendous therapeutic potential, and one for which growth and differentiation conditions are poorly characterized and far from defined and optimized. A standard ACME screen uses the technologies previously applied to the manufacture and analysis of DNA microarrays, requires standard cell-culture facilities and can be performed from beginning to end within 5-10 days.
引用
收藏
页码:703 / 717
页数:15
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