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使用可自擦除的仙台病毒载体生成无足迹的犬诱导多能干细胞。

Generation of Footprint-Free Canine Induced Pluripotent Stem Cells Using Auto-Erasable Sendai Virus Vector.

机构信息

1 Department of Advanced Pathobiology, Graduate School of Life and Environmental Sciences, Osaka Prefecture University , Izumisano, Japan .

2 Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine , Stanford, California.

出版信息

Stem Cells Dev. 2018 Nov 15;27(22):1577-1586. doi: 10.1089/scd.2018.0084. Epub 2018 Oct 11.

Abstract

Canine induced pluripotent stem cells (ciPSCs) can be used in regenerative medicine. However, there are no reports on the generation of genome integration-free and completely exogenous gene-silenced (footprint free) ciPSCs that are tolerant to enzymatic single-cell passage. In this study, we reprogrammed canine embryonic fibroblasts using the auto-erasable replication-defective and persistent Sendai virus vector, SeVdp(KOSM)302L, and generated two ciPSC lines. The ciPSCs were positive for pluripotent markers, including alkaline phosphatase activity as well as OCT3/4, SOX2, and NANOG transcripts, and NANOG, stage-specific embryonic antigen-1, and partial TRA-1-60 protein expression, even after SeVdp(KOSM)302L removal. The ciPSCs were induced to differentiate into all the three germ layers as embryoid bodies in vitro and as teratomas in vivo. Furthermore, SeVdp(KOSM)302L-free ciPSCs maintained a normal karyotype even after repeated enzymatic single-cell passaging. Therefore, to our knowledge, for the first time, we demonstrated the generation of footprint-free and high-quality ciPSCs that can be passaged at the single-cell stage using enzymatic methods. Our method for generation of ciPSCs is a good step toward the development of clinical application of ciPSCs.

摘要

犬诱导多能干细胞(ciPSCs)可用于再生医学。然而,目前尚无关于生成基因组整合-free 和完全外源性基因沉默(无印迹)ciPSCs 的报道,这些 ciPSCs 耐受酶消化单细胞传代。在这项研究中,我们使用可自我擦除的复制缺陷型和持续型仙台病毒载体 SeVdp(KOSM)302L 对犬胚胎成纤维细胞进行重编程,生成了两条 ciPSC 系。ciPSCs 表达多能性标志物,包括碱性磷酸酶活性以及 OCT3/4、SOX2 和 NANOG 转录物,并且在 SeVdp(KOSM)302L 去除后表达 NANOG、阶段特异性胚胎抗原-1 和部分 TRA-1-60 蛋白。ciPSCs 在体外诱导分化为胚状体,并在体内诱导分化为畸胎瘤,形成三个胚层。此外,SeVdp(KOSM)302L-free ciPSCs 在反复酶消化单细胞传代后仍保持正常核型。因此,据我们所知,这是首次证明可以使用酶法在单细胞阶段传代生成无印迹和高质量的 ciPSCs。我们生成 ciPSCs 的方法是向 ciPSCs 的临床应用迈出的良好一步。

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