Interdisciplinary Nanoscience Center (iNANO), Arhus University, Arhus, Denmark.
Stem Cells Dev. 2009 Nov;18(9):1331-42. doi: 10.1089/scd.2009.0114.
The potential of embryonic stem (ES) cells for both self-renewal and differentiation into cells of all three germ layers has generated immense interest in utilizing these cells for tissue engineering or cell-based therapies. However, the ability to culture undifferentiated ES cells without the use of feeder cells as well as means to obtain homogeneous, differentiated cell populations devoid of residual pluripotent ES cells still remain major challenges. Here we have applied murine ES cells to topographically microstructured surface libraries, BioSurface Structure Arrays (BSSA), and investigated whether these could be used to (i) identify topographically microstructured growth supports alleviating the need for feeder cells for expansion of undifferentiated ES cells and (ii) identify specific types of microstructures enforcing differentiation of ES cells. The BSSA surfaces arrays consisted of 504 different topographical microstructures each located in a tester field of 3 x 3 mm. The murine ES cell lines CJ7 and KH2 were seeded upon the BSSA libraries and specific topographical structures facilitating either undifferentiated ES cell growth or enhancing spreading indicative of differentiation of the ES cells were identified. Secondly serial passage of undifferentiated CJ7 ES cells on selected microstructures, identified in the screening of these BSSA libraries, showed that these cells had retained germ-line potential. These results indicate that one specific type of topographical surface microstructures, identified by the BSSA technology, can substitute for feeder cells and that another subset may be used to eliminate undifferentiated ES cells from a population of differentiated ES cells.
胚胎干细胞 (ES) 具有自我更新和分化为三个胚层细胞的潜力,这为利用这些细胞进行组织工程或基于细胞的治疗方法带来了巨大的兴趣。然而,能够在不使用饲养细胞的情况下培养未分化的 ES 细胞,以及获得均质的、分化细胞群体而不残留多能 ES 细胞的方法仍然是主要的挑战。在这里,我们将鼠 ES 细胞应用于形貌微结构化表面文库(BioSurface Structure Arrays,BSSA),并研究了这些方法是否可以用于:(i)鉴定形貌微结构化的生长支持物,以缓解未分化 ES 细胞扩增对饲养细胞的需求;(ii)鉴定特定类型的微结构,以促进 ES 细胞的分化。BSSA 表面文库由 504 种不同的形貌微结构组成,每种微结构位于 3x3mm 的测试场中。将鼠 ES 细胞系 CJ7 和 KH2 接种于 BSSA 文库上,并鉴定出有利于未分化 ES 细胞生长或促进细胞扩散的特定形貌结构,表明这些 ES 细胞发生了分化。其次,在筛选这些 BSSA 文库时,选择能够促进未分化 CJ7 ES 细胞增殖的特定微结构进行连续传代,结果表明这些细胞保留了生殖系潜能。这些结果表明,BSSA 技术鉴定的一种特定类型的形貌表面微结构可以替代饲养细胞,而另一子集可能用于从分化的 ES 细胞群体中消除未分化的 ES 细胞。