Lee Minhyung, Ha Jeongmin, Son Ye Seul, Ahn Hyunjun, Jung Kwang Bo, Son Mi-Young, Kim Janghwan
Stem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea.
Department of Functional Genomics, KRIBB School of Bioscience, Korea University of Science and Technology, Daejeon, 34113, Republic of Korea.
Exp Mol Med. 2019 Jul 19;51(7):1-12. doi: 10.1038/s12276-019-0282-7.
Reprogramming with episomal vectors is an easy, safe, and cost-effective method to generate exogenous DNA-free (exogene-free) induced pluripotent stem cells (iPSCs). However, the genomic integration of exogenes is observed occasionally. Additionally, the removal of episomal DNA takes more than 70 days in established iPSCs. Here, we inserted the cytosine deaminase (CD) gene from yeast into episomal vectors and used them to reprogram human fibroblasts into iPSCs. These new episomal vectors (CD episomal vectors) were eliminated from the generated iPSCs as early as seven days after 5-fluorocytosine (5-FC) treatment. We also found that cells with the integration of the CD gene perished within two days of 5-FC treatment. In addition, we generated exogene-free induced neural stem cells after one passage by direct reprogramming with CD episomal vectors combined with 5-FC treatment. Conclusively, our novel method allows the rapid and easy isolation of exogene-free reprogrammed cells and can be applied to disease modeling and clinical applications.
使用附加型载体进行重编程是一种简单、安全且经济高效的方法,可用于生成无外源DNA(无外基因)的诱导多能干细胞(iPSC)。然而,偶尔会观察到外基因的基因组整合。此外,在已建立的iPSC中,去除附加型DNA需要70多天。在此,我们将来自酵母的胞嘧啶脱氨酶(CD)基因插入附加型载体,并使用它们将人成纤维细胞重编程为iPSC。这些新的附加型载体(CD附加型载体)在5-氟胞嘧啶(5-FC)处理后最早7天就从生成的iPSC中消除。我们还发现,整合了CD基因的细胞在5-FC处理后两天内死亡。此外,通过用CD附加型载体结合5-FC处理进行直接重编程,我们在传代一次后生成了无外基因的诱导神经干细胞。总之,我们的新方法能够快速简便地分离无外基因的重编程细胞,可应用于疾病建模和临床应用。