Kim Sung Min, Kim Jong-Wan, Kwak Tae Hwan, Park Sang Woong, Kim Kee-Pyo, Park Hyunji, Lim Kyung Tae, Kang Kyuree, Kim Jonghun, Yang Ji Hun, Han Heonjong, Lee Insuk, Hyun Jung Keun, Bae Young Min, Schöler Hans R, Lee Hoon Taek, Han Dong Wook
Department of Stem Cell Biology, School of Medicine, 1 Hwayang-dong, Gwangjin-gu, Seoul 05029, Republic of Korea; Department of Animal Biotechnology, Konkuk University, 1 Hwayang-dong, Gwangjin-gu, Seoul 05029, Republic of Korea.
Department of Nanobiomedical Science, Dankook University Graduate School, Cheonan 31116, Republic of Korea.
J Biol Chem. 2016 Jul 1;291(27):14199-14212. doi: 10.1074/jbc.M115.713578. Epub 2016 May 4.
The viral vector-mediated overexpression of the defined transcription factors, Brn4/Pou3f4, Sox2, Klf4, and c-Myc (BSKM), could induce the direct conversion of somatic fibroblasts into induced neural stem cells (iNSCs). However, viral vectors may be randomly integrated into the host genome thereby increasing the risk for undesired genotoxicity, mutagenesis, and tumor formation. Here we describe the generation of integration-free iNSCs from mouse fibroblasts by non-viral episomal vectors containing BSKM. The episomal vector-derived iNSCs (e-iNSCs) closely resemble control NSCs, and iNSCs generated by retrovirus (r-iNSCs) in morphology, gene expression profile, epigenetic status, and self-renewal capacity. The e-iNSCs are functionally mature, as they could differentiate into all the neuronal cell types both in vitro and in vivo Our study provides a novel concept for generating functional iNSCs using a non-viral, non-integrating, plasmid-based system that could facilitate their biomedical applicability.
病毒载体介导的特定转录因子Brn4/Pou3f4、Sox2、Klf4和c-Myc(BSKM)的过表达可诱导体细胞成纤维细胞直接转化为诱导神经干细胞(iNSCs)。然而,病毒载体可能会随机整合到宿主基因组中,从而增加产生不良基因毒性、诱变和肿瘤形成的风险。在此,我们描述了通过含有BSKM的非病毒游离载体从小鼠成纤维细胞生成无整合iNSCs的方法。游离载体衍生的iNSCs(e-iNSCs)在形态、基因表达谱、表观遗传状态和自我更新能力方面与对照神经干细胞以及逆转录病毒生成的iNSCs(r-iNSCs)极为相似。e-iNSCs功能成熟,因为它们在体外和体内均可分化为所有神经元细胞类型。我们的研究提供了一种新的概念,即使用基于质粒的非病毒、非整合系统来生成功能性iNSCs,这有助于其在生物医学中的应用。