Arai Yoshikazu, Ohgane Jun, Fujishiro Shuh-hei, Nakano Kazuaki, Matsunari Hitomi, Watanabe Masahito, Umeyama Kazuhiro, Azuma Dai, Uchida Naomi, Sakamoto Nozomu, Makino Tomohiro, Yagi Shintaro, Shiota Kunio, Hanazono Yutaka, Nagashima Hiroshi
Department of Life Sciences, Laboratory of Developmental Engineering, School of Agriculture, Meiji University, Kanagawa, Japan.
Genesis. 2013 Nov;51(11):763-76. doi: 10.1002/dvg.22423. Epub 2013 Aug 30.
Porcine induced pluripotent stem cells (iPSCs) provide useful information for translational research. The quality of iPSCs can be assessed by their ability to differentiate into various cell types after chimera formation. However, analysis of chimera formation in pigs is a labor-intensive and costly process, necessitating a simple evaluation method for porcine iPSCs. Our previous study identified mouse embryonic stem cell (ESC)-specific hypomethylated loci (EShypo-T-DMRs), and, in this study, 36 genes selected from these were used to evaluate porcine iPSC lines. Based on the methylation profiles of the 36 genes, the iPSC line, Porco Rosso-4, was found closest to mouse pluripotent stem cells among 5 porcine iPSCs. Moreover, Porco Rosso-4 more efficiently contributed to the inner cell mass (ICM) of blastocysts than the iPSC line showing the lowest reprogramming of the 36 genes (Porco Rosso-622-14), indicating that the DNA methylation profile correlates with efficiency of ICM contribution. Furthermore, factors known to enhance iPSC quality (serum-free medium with PD0325901 and CHIR99021) improved the methylation status at the 36 genes. Thus, the DNA methylation profile of these 36 genes is a viable index for evaluation of porcine iPSCs.
猪诱导多能干细胞(iPSC)为转化研究提供了有用信息。iPSC的质量可通过其在嵌合体形成后分化为各种细胞类型的能力来评估。然而,猪嵌合体形成的分析是一个劳动密集型且成本高昂的过程,因此需要一种简单的猪iPSC评估方法。我们之前的研究鉴定出了小鼠胚胎干细胞(ESC)特异性低甲基化位点(EShypo-T-DMR),在本研究中,从这些位点中选取的36个基因被用于评估猪iPSC系。基于这36个基因的甲基化谱,在5个猪iPSC中,发现“红猪-4”(Porco Rosso-4)iPSC系与小鼠多能干细胞最为接近。此外,与36个基因重编程程度最低的iPSC系(“红猪-622-14”,Porco Rosso-622-14)相比,“红猪-4”对囊胚内细胞团(ICM)的贡献效率更高,这表明DNA甲基化谱与ICM贡献效率相关。此外,已知能提高iPSC质量的因素(添加PD0325901和CHIR99021的无血清培养基)改善了这36个基因的甲基化状态。因此,这36个基因的DNA甲基化谱是评估猪iPSC的一个可行指标。