Matsumoto Ryo, Shimizu Kazunori, Nagashima Takunori, Tanaka Hiromasa, Mizuno Masaaki, Kikkawa Fumitaka, Hori Masaru, Honda Hiroyuki
Department of Biotechnology, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.
Institute of Innovation for Future Society, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Regen Ther. 2016 Sep 10;5:55-63. doi: 10.1016/j.reth.2016.07.001. eCollection 2016 Dec.
Human pluripotent stem cells, including human induced pluripotent stem cells (hiPSCs), are promising materials for regenerative medicine and cell transplantation therapy. However, tumorigenic potential of residual undifferentiated stem cells hampers their use in these therapies. Therefore, it is important to develop methods that selectively eliminate undifferentiated stem cells from a population of differentiated cells before their transplantation. In the present study, we investigated whether plasma-activated medium (PAM) selectively eliminated undifferentiated hiPSCs by inducing external oxidative stress. PAM was prepared by irradiating cell culture medium with non-thermal atmospheric pressure plasma. We observed that PAM selectively and efficiently killed undifferentiated hiPSCs cocultured with normal human dermal fibroblasts (NHDFs), which were used as differentiated cells. We also observed that undifferentiated hiPSCs were more sensitive to PAM than hiPSC-derived differentiated cells. Gene expression analysis suggested that lower expression of oxidative stress-related genes, including those encoding enzymes involved in hydrogen peroxide (HO) degradation, in undifferentiated hiPSCs was one of the mechanisms underlying PAM-induced selective cell death. PAM killed undifferentiated hiPSCs more efficiently than a medium containing the same concentration of HO as that in PAM, suggesting that HO and various reactive oxygen/nitrogen species in PAM selectively eliminated undifferentiated hiPSCs. Thus, our results indicate that PAM has a great potential to eliminate tumorigenic hiPSCs from a population of differentiated cells and that it may be a very useful tool in regenerative medicine and cell transplantation therapy.
人类多能干细胞,包括人类诱导多能干细胞(hiPSC),是再生医学和细胞移植治疗中很有前景的材料。然而,残留未分化干细胞的致瘤潜力阻碍了它们在这些治疗中的应用。因此,开发在移植前从分化细胞群体中选择性清除未分化干细胞的方法很重要。在本研究中,我们调查了血浆激活培养基(PAM)是否通过诱导外部氧化应激来选择性清除未分化的hiPSC。PAM是通过用非热大气压等离子体照射细胞培养基制备的。我们观察到,PAM能选择性且有效地杀死与正常人皮肤成纤维细胞(NHDF)共培养的未分化hiPSC,NHDF用作分化细胞。我们还观察到,未分化的hiPSC比hiPSC来源的分化细胞对PAM更敏感。基因表达分析表明,未分化hiPSC中氧化应激相关基因(包括编码参与过氧化氢(HO)降解的酶的基因)的低表达是PAM诱导选择性细胞死亡的机制之一。PAM比含有与PAM中相同浓度HO的培养基更有效地杀死未分化的hiPSC,这表明PAM中的HO和各种活性氧/氮物种选择性清除了未分化的hiPSC。因此,我们的结果表明,PAM在从分化细胞群体中清除致瘤性hiPSC方面具有很大潜力,并且它可能是再生医学和细胞移植治疗中非常有用的工具。