Controlled-size embryoid body formation in concave microwell arrays

被引:236
作者
Choi, Yoon Young [1 ]
Chung, Bong Geun [2 ]
Lee, Dae Ho [1 ]
Khademhosseini, Ali [3 ,4 ]
Kim, Jong-Hoon [5 ]
Lee, Sang-Hoon [1 ]
机构
[1] Korea Univ, Dept Biomed Engn, Seoul 136701, South Korea
[2] Hanyang Univ, Dept Bionano Engn, Ansan 426791, South Korea
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Biomed Engn,Dept Med, Cambridge, MA 02139 USA
[4] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[5] Korea Univ, Coll Life Sci & Biotechnol, Div Biotechnol, Seoul 136705, South Korea
关键词
Concave microwell array; Embryonic stem cell differentiation; Neurogenesis; Cardiogenesis; IN-VITRO DIFFERENTIATION; STEM-CELLS; SOFT LITHOGRAPHY; MEDIATED CONTROL; BODIES; FABRICATION; CULTURE; BIOLOGY; MICROFABRICATION; CARDIOMYOCYTES;
D O I
10.1016/j.biomaterials.2010.01.115
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Embryonic stem (ES) cells hold great potential as a renewable cell source for regenerative medicine and cell-based therapy. Despite the potential of ES cells, conventional stem cell culture methods do not enable the control of the microenvironment. A number of microscale engineering approaches have been recently developed to control the extracellular microenvironment and to direct embryonic stem cell fate. Here, we used engineered concave microwell arrays to regulate the size and shape of embryoid bodies (EBs) cell aggregate intermediates derived from ES cells. Murine ES cells were aggregated within concave microwells, and their aggregate sizes were controlled by varying the microwell widths (200, 500, and 1000 mu m). Differentiation of murine ES cells into three germ layers was assessed by analyzing gene expression. We found that ES cell-derived cardiogenesis and neurogenesis were strongly regulated by the EB size, showing that larger concave microwell arrays induced more neuronal and cardiomyocyte differentiation than did smaller microwell arrays. Therefore, this engineered concave microwell array could be a potentially useful tool for controlling ES cell behavior. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4296 / 4303
页数:8
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