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

机译:三维支架结构对小鼠胚胎干细胞干性维持的重要性

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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.
机译: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很重要。传统的二维(2D)培养的mES细胞与体内等效内细胞团(ICM)处于非常不同的2D生态位。因为细胞命运的决定可能受几何形状影响的许多线索的控制,所以传统的2D培养系统将妨碍我们正确理解体内情况。人们认为三维(3D)支架可提供与体内封闭的3D环境。在这项工作中,准备了三种不同的支架用于细胞培养。与2D相比,在3D支架培养下mES细胞的几个特征发生了变化,这些变化主要是由于几何结构的改变,而不是基质的改变。通过引入维数来促进mES细胞的自我更新。在长期培养中,所有三个没有饲养细胞的3D支架都支持mES的干性维持。我们的发现表明,支架的3D几何结构促进了mES细胞的干性维持,这将为ES细胞研究提供有希望的平台。 (C)2014 Elsevier Ltd.保留所有权利。

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