Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, Japan.
Institute for Protein Research, Osaka University, Osaka 565-0871, Japan.
Sci Rep. 2014 Jan 8;4:3594. doi: 10.1038/srep03594.
In order to apply human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs) to regenerative medicine, the cells should be produced under restricted conditions conforming to GMP guidelines. Since the conventional culture system has some issues that need to be addressed to achieve this goal, we developed a novel culture system. We found that recombinant laminin-511 E8 fragments are useful matrices for maintaining hESCs and hiPSCs when used in combination with a completely xeno-free (Xf) medium, StemFit™. Using this system, hESCs and hiPSCs can be easily and stably passaged by dissociating the cells into single cells for long periods, without any karyotype abnormalities. Human iPSCs could be generated under feeder-free (Ff) and Xf culture systems from human primary fibroblasts and blood cells, and they possessed differentiation abilities. These results indicate that hiPSCs can be generated and maintained under this novel Ff and Xf culture system.
为了将人类胚胎干细胞(hESCs)和诱导多能干细胞(hiPSCs)应用于再生医学,这些细胞应在符合 GMP 指南的受限条件下产生。由于传统的培养系统存在一些需要解决的问题,我们开发了一种新的培养系统。我们发现,重组层粘连蛋白-511 E8 片段与完全无动物源(Xf)培养基 StemFitTM 结合使用时,对于维持 hESCs 和 hiPSCs 非常有用。使用该系统,通过将细胞解离成单细胞,可以长时间轻松且稳定地传代 hESCs 和 hiPSCs,而不会出现任何染色体异常。可以从人原代成纤维细胞和血细胞中在无饲养层(Ff)和 Xf 培养系统下生成人 iPSCs,并且它们具有分化能力。这些结果表明,可以在这种新型 Ff 和 Xf 培养系统下生成和维持 hiPSCs。