The importance of three-dimensional scaffold structure on stemness maintenance of mouse embryonic stem cells

被引:68
作者
Wei, Jianshu [1 ,2 ]
Han, Jin [1 ]
Zhao, Yannan [1 ]
Cui, Yi [1 ]
Wang, Bin [1 ]
Xiao, Zhifeng [1 ]
Chen, Bing [1 ]
Dai, Jianwu [1 ]
机构
[1] Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Mol Dev Biol, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100190, Peoples R China
关键词
Three-dimensional scaffold; mES cells; Stemness; Geometry; FEEDER-FREE CULTURE; SELF-RENEWAL; EXTRACELLULAR-MATRIX; COLLAGEN SCAFFOLDS; SIGNALING PATHWAYS; E-CADHERIN; DIFFERENTIATION; INTEGRINS; HYPOXIA; PLURIPOTENCY;
D O I
10.1016/j.biomaterials.2014.05.060
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
Revealing the mechanisms of cell fate regulation is important for scientific research and stem cell-based therapy. The traditional two-dimensional (2D) cultured mES cells are in a very different 2D niche from the in vivo equivalent-inner cell mass (ICM). Because the cell fate decision could be regulated by many cues which could be impacted by geometry, the traditional 2D culture system would hamper us from understanding the in vivo situations correctly. Three-dimensional (3D) scaffold was believed to provide a 3D environment closed to the in vivo one. In this work, three different scaffolds were prepared for cell culture. Several characters of mES cells were changed under 3D scaffolds culture compared to 2D, and these changes were mainly due to the alteration in geometry but not the matrix. The self-renewal of mES cells was promoted by the introducing of dimensionality. The stemness maintenance of mES was supported by all three 3D scaffolds without feeder cells in the long-time culture. Our findings demonstrated that the stemness maintenance of mES cells was promoted by the 3D geometry of scaffolds and this would provide a promising platform for ES cell research. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7724 / 7733
页数:10
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