State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China; Graduate School, ChineseAcademy of Sciences, Beijing 100190, China.
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Biomaterials. 2014 Sep;35(27):7724-33. doi: 10.1016/j.biomaterials.2014.05.060. Epub 2014 Jun 12.
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.
揭示细胞命运调控的机制对于科学研究和基于干细胞的治疗非常重要。传统的二维(2D)培养的 mES 细胞与体内等效的内细胞团(ICM)所处的 2D 生态位非常不同。由于细胞命运的决定可能受到许多可以受到几何形状影响的线索的调节,因此传统的 2D 培养系统会阻碍我们正确理解体内情况。三维(3D)支架被认为提供了更接近体内环境的 3D 环境。在这项工作中,为细胞培养准备了三种不同的支架。与 2D 相比,mES 细胞在 3D 支架培养下的几个特征发生了变化,这些变化主要归因于几何形状的改变而不是基质。通过引入维度促进了 mES 细胞的自我更新。在没有饲养细胞的长时间培养中,这三种 3D 支架都支持 mES 的干性维持。我们的研究结果表明,mES 细胞的干性维持是由支架的 3D 几何形状促进的,这将为 ES 细胞研究提供一个有前途的平台。