Tano Keiko, Yasuda Satoshi, Kuroda Takuya, Saito Hirohisa, Umezawa Akihiro, Sato Yoji
Department of Reproductive Biology, National Research Institute for Child Health and Development, Tokyo, Japan; Division of Cellular & Gene Therapy Products, National Institute of Health Sciences, Tokyo, Japan.
Division of Cellular & Gene Therapy Products, National Institute of Health Sciences, Tokyo, Japan.
PLoS One. 2014 Oct 27;9(10):e110496. doi: 10.1371/journal.pone.0110496. eCollection 2014.
Innovative applications of cell therapy products (CTPs) derived from human pluripotent stem cells (hPSCs) in regenerative medicine are currently being developed. The presence of residual undifferentiated hPSCs in CTPs is a quality concern associated with tumorigencity. However, no simple in vitro method for direct detection of undifferentiated hPSCs that contaminate CTPs has been developed. Here, we show a novel approach for direct and sensitive detection of a trace amount of undifferentiated human induced pluripotent stem cells (hiPSCs) using a highly efficient amplification method in combination with laminin-521 and Essential 8 medium. Essential 8 medium better facilitated the growth of hiPSCs dissociated into single cells on laminin-521 than in mTeSR1 medium. hiPSCs cultured on laminin-521 in Essential 8 medium were maintained in an undifferentiated state and they maintained the ability to differentiate into various cell types. Essential 8 medium allowed robust hiPSC proliferation plated on laminin-521 at low cell density, whereas mTeSR1 did not enhance the cell growth. The highly efficient culture system using laminin-521 and Essential 8 medium detected hiPSCs spiked into primary human mesenchymal stem cells (hMSCs) or human neurons at the ratio of 0.001%-0.01% as formed colonies. Moreover, this assay method was demonstrated to detect residual undifferentiated hiPSCs in cell preparations during the process of hMSC differentiation from hiPSCs. These results indicate that our highly efficient amplification system using a combination of laminin-521 and Essential 8 medium is able to detect a trace amount of undifferentiated hPSCs contained as impurities in CTPs and would contribute to quality assessment of hPSC-derived CTPs during the manufacturing process.
目前正在开发源自人类多能干细胞(hPSC)的细胞治疗产品(CTP)在再生医学中的创新应用。CTP中残留未分化的hPSC的存在是与致瘤性相关的质量问题。然而,尚未开发出用于直接检测污染CTP的未分化hPSC的简单体外方法。在此,我们展示了一种新颖的方法,使用高效扩增方法结合层粘连蛋白-521和Essential 8培养基,直接且灵敏地检测痕量未分化的人类诱导多能干细胞(hiPSC)。与mTeSR1培养基相比,Essential 8培养基更有利于解离成单细胞的hiPSC在层粘连蛋白-521上生长。在Essential 8培养基中于层粘连蛋白-521上培养的hiPSC保持未分化状态,并维持分化为各种细胞类型的能力。Essential 8培养基允许以低细胞密度接种在层粘连蛋白-521上的hiPSC强劲增殖,而mTeSR1则不能促进细胞生长。使用层粘连蛋白-521和Essential 8培养基的高效培养系统检测到以0.001%-0.01%的比例掺入原代人间充质干细胞(hMSC)或人类神经元中的hiPSC形成的集落。此外,该检测方法被证明可检测hiPSC向hMSC分化过程中细胞制剂中残留的未分化hiPSC。这些结果表明,我们使用层粘连蛋白-521和Essential 8培养基组合的高效扩增系统能够检测CTP中作为杂质包含的痕量未分化hPSC,并将有助于在制造过程中对源自hPSC的CTP进行质量评估。