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本文引用的文献

1
Induced neural stem cells from distinct genetic backgrounds exhibit different reprogramming status.来自不同遗传背景的诱导神经干细胞表现出不同的重编程状态。
Stem Cell Res. 2016 Mar;16(2):460-8. doi: 10.1016/j.scr.2016.02.025. Epub 2016 Feb 10.
2
Single Transcription Factor Conversion of Human Blood Fate to NPCs with CNS and PNS Developmental Capacity.将人类血液命运转化为具有中枢神经系统和外周神经系统发育能力的神经前体细胞的单一转录因子转换
Cell Rep. 2015 Jun 9;11(9):1367-76. doi: 10.1016/j.celrep.2015.04.056. Epub 2015 May 21.
3
Direct lineage conversion of adult mouse liver cells and B lymphocytes to neural stem cells.直接将成年小鼠的肝细胞和 B 淋巴细胞转化为神经干细胞。
Stem Cell Reports. 2014 Dec 9;3(6):948-56. doi: 10.1016/j.stemcr.2014.10.001. Epub 2014 Nov 6.
4
A comparison of non-integrating reprogramming methods.非整合重编程方法的比较。
Nat Biotechnol. 2015 Jan;33(1):58-63. doi: 10.1038/nbt.3070. Epub 2014 Dec 1.
5
Therapeutic potential of induced neural stem cells for spinal cord injury.诱导神经干细胞对脊髓损伤的治疗潜力。
J Biol Chem. 2014 Nov 21;289(47):32512-25. doi: 10.1074/jbc.M114.588871. Epub 2014 Oct 6.
6
Induced neural stem cells achieve long-term survival and functional integration in the adult mouse brain.诱导性神经干细胞在成年小鼠大脑中实现长期存活和功能整合。
Stem Cell Reports. 2014 Sep 9;3(3):423-31. doi: 10.1016/j.stemcr.2014.06.017. Epub 2014 Jul 31.
7
Direct conversion of mouse fibroblasts into induced neural stem cells.直接将小鼠成纤维细胞转化为诱导性神经干细胞。
Nat Protoc. 2014 Apr;9(4):871-81. doi: 10.1038/nprot.2014.056. Epub 2014 Mar 20.
8
Direct reprogramming of human fibroblasts to functional and expandable hepatocytes.人成纤维细胞直接重编程为功能性和可扩增的肝细胞。
Cell Stem Cell. 2014 Mar 6;14(3):370-84. doi: 10.1016/j.stem.2014.01.003. Epub 2014 Feb 27.
9
Human hepatocytes with drug metabolic function induced from fibroblasts by lineage reprogramming.由谱系重编程诱导的具有药物代谢功能的人肝细胞。
Cell Stem Cell. 2014 Mar 6;14(3):394-403. doi: 10.1016/j.stem.2014.01.008. Epub 2014 Feb 27.
10
Generation of integration-free and region-specific neural progenitors from primate fibroblasts.从灵长类成纤维细胞中生成无整合和区域特异性的神经祖细胞。
Cell Rep. 2013 May 30;3(5):1580-91. doi: 10.1016/j.celrep.2013.04.004. Epub 2013 May 2.

从小鼠成纤维细胞中生成无整合诱导神经干细胞。

Generation of Integration-free Induced Neural Stem Cells from Mouse Fibroblasts.

作者信息

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

机构信息

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.

出版信息

J Biol Chem. 2016 Jul 1;291(27):14199-14212. doi: 10.1074/jbc.M115.713578. Epub 2016 May 4.

DOI:10.1074/jbc.M115.713578
PMID:27189941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4933177/
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.

摘要

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。