| Literature DB >> 27189941 |
Sung Min Kim1, Jong-Wan Kim2, Tae Hwan Kwak3, Sang Woong Park4, Kee-Pyo Kim5, Hyunji Park4, Kyung Tae Lim3, Kyuree Kang3, Jonghun Kim3, Ji Hun Yang5, Heonjong Han6, Insuk Lee6, Jung Keun Hyun2, Young Min Bae4, Hans R Schöler7, Hoon Taek Lee8, Dong Wook Han9.
Abstract
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.Entities:
Keywords: cell biology; cell therapy; neural stem cell (NSC); regenerative medicine; reprogramming
Mesh:
Year: 2016 PMID: 27189941 PMCID: PMC4933177 DOI: 10.1074/jbc.M115.713578
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157