Embryoid body size-mediated differential endodermal and mesodermal differentiation using polyethylene glycol (PEG) microwell array

被引:12
作者
Cha, Jae Min [1 ,2 ,3 ]
Bae, Hojae [4 ,5 ]
Sadr, Nasser [1 ,2 ,6 ,7 ]
Manoucheri, Sam [1 ,2 ]
Edalat, Faramarz [1 ,2 ]
Kim, Keekyoung [1 ,2 ,6 ]
Kim, Sang Bok [1 ,2 ]
Kwon, Il Keun [4 ,5 ]
Hwang, Yu-Shik [4 ,5 ]
Khademhosseini, Ali [1 ,2 ,4 ,5 ,6 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Dept Med, Sch Med,Ctr Biomed Engn, Boston, MA 02118 USA
[2] MIT, Harvard MIT Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] Samsung Elect Co Ltd, Samsung Biomed Res Inst, SAIT, Seoul 135710, South Korea
[4] Kyung Hee Univ, Sch Dent, Dept Maxillofacial Biomed Engn, Seoul 130701, South Korea
[5] Kyung Hee Univ, Inst Oral Biol, Sch Dent, Seoul 130701, South Korea
[6] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[7] Politecn Milan, Dept Bioengn, I-20131 Milan, Italy
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
microwell; embryoid body size; differentiation; lateral plate mesoderm; visceral endoderm; STEM-CELL DIFFERENTIATION; GENE-EXPRESSION; VISCERAL ENDODERM; CARDIAC MESODERM; INDIAN HEDGEHOG; IN-VITRO; TRANSCRIPTION; MORPHOGENESIS; GASTRULATION; MESENDODERM;
D O I
10.1007/s13233-015-3034-0
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Embryoid bodies have a number of similarities with cells in gastrulation, which provides useful biological information about embryonic stem cell differentiation. Extensive research has been done to study the control of embryoid body-mediated embryonic stem cell differentiation in various research fields. Recently, microengineering technology has been used to control the size of embryoid bodies and to direct lineage specific differentiation of embryonic stem cells. However, the underlying biology of developmental events in the embryoid bodies of different sizes has not been well elucidated. In this study, embryoid bodies with different sizes were generated within microfabricated PEG microwell arrays, and a series of gene and molecular expressions related to early developmental events was investigated to further elucidate the size-mediated differentiation. The gene and molecular expression profile suggested preferential visceral endoderm formation in 450 mu m embryoid bodies and preferential lateral plate mesoderm formation in 150 mu m embryoid bodies. These aggregates resulted in higher cardiac differentiation in 450 mu m embryoid bodies and higher endothelial differentiation in 150 mu m embryoid bodies, respectively. Our findings may provide further insight for understanding embryoid body size-mediated developmental progress.
引用
收藏
页码:245 / 255
页数:11
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