Tunable shrink-induced honeycomb microwell arrays for uniform embryoid bodies

被引:39
|
作者
Nguyen, Diep [1 ]
Sa, Silin [2 ]
Pegan, Jonathan D. [3 ]
Rich, Brent [3 ]
Xiang, Guangxin [2 ]
McCloskey, Kara E. [2 ]
Manilay, Jennifer O. [4 ]
Khine, Michelle [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92717 USA
[2] Univ Calif, Grad Grp Biol Engn & Small Scale Technol, Merced, CA USA
[3] Univ Calif, Sch Engn, Merced, CA USA
[4] Univ Calif Merced, Sch Nat Sci, Merced, CA USA
关键词
STEM-CELL DIFFERENTIATION; IN-VITRO DIFFERENTIATION; COLONY-FORMING CELLS; MICROFLUIDIC DEVICES; DINK MICROFLUIDICS; GENE-EXPRESSION; CULTURE; SYSTEM; GENERATION; INHIBITOR;
D O I
10.1039/b914091c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Embryoid body (EB) formation closely recapitulates early embryonic development with respect to lineage commitment. Because it is greatly affected by cell-cell and cell-substrate interactions, the ability to control the initial number of cells in the aggregates and to provide an appropriate substrate are crucial parameters for uniform EB formation. Here we report of an ultra-rapid fabrication and culture method utilizing a laser-jet printer to generate closely arrayed honeycomb microwells of tunable sizes for the induction of uniform EBs from single cell suspension. By printing various microwell patterns onto pre-stressed polystyrene sheets, and through heat induced shrinking, high aspect micromolds are generated. Notably, we achieve rounded bottom polydimethylsiloxane (PDMS) wells not easily achievable with standard microfabrication methods, but critical to achieve spherical EBs. Furthermore, by simply controlling the size of the microwells and the concentration of the cell suspension we can control the initial size of the cell aggregate, thus influencing lineage commitment. In addition, these microwells are easily adaptable and scalable to most standard well plates and easily integrated into commercial liquid handling systems to provide an inexpensive and easy high throughput compound screening platform.
引用
收藏
页码:3338 / 3344
页数:7
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