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本文引用的文献

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Direct reprogramming of mouse and human fibroblasts into multipotent neural stem cells with a single factor.将小鼠和人成纤维细胞直接重编程为具有单一因子的多能神经干细胞。
Cell Stem Cell. 2012 Jul 6;11(1):100-9. doi: 10.1016/j.stem.2012.05.018. Epub 2012 Jun 7.
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Heart repair by reprogramming non-myocytes with cardiac transcription factors.心脏转录因子对非心肌细胞的重编程实现心脏修复。
Nature. 2012 May 13;485(7400):599-604. doi: 10.1038/nature11139.
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Neural stem cells: mechanisms and modeling.神经干细胞:机制与建模。
Protein Cell. 2012 Apr;3(4):251-61. doi: 10.1007/s13238-012-2033-6. Epub 2012 May 2.
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Direct conversion of fibroblasts into stably expandable neural stem cells.成纤维细胞直接转化为稳定扩增的神经干细胞。
Cell Stem Cell. 2012 Apr 6;10(4):473-9. doi: 10.1016/j.stem.2012.03.003. Epub 2012 Mar 22.
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Direct reprogramming of fibroblasts into neural stem cells by defined factors.通过定义因子将成纤维细胞直接重编程为神经干细胞。
Cell Stem Cell. 2012 Apr 6;10(4):465-72. doi: 10.1016/j.stem.2012.02.021. Epub 2012 Mar 22.
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Trans-differentiation of neural stem cells: a therapeutic mechanism against the radiation induced brain damage.神经干细胞的转分化:一种针对放射性脑损伤的治疗机制。
PLoS One. 2012;7(2):e25936. doi: 10.1371/journal.pone.0025936. Epub 2012 Feb 10.
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Direct conversion of mouse fibroblasts to self-renewing, tripotent neural precursor cells.直接将小鼠成纤维细胞转化为具有自我更新能力的、三能性神经前体细胞。
Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2527-32. doi: 10.1073/pnas.1121003109. Epub 2012 Jan 30.
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Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells.利用诱导多能干细胞探究散发性和家族性阿尔茨海默病。
Nature. 2012 Jan 25;482(7384):216-20. doi: 10.1038/nature10821.
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Intronic miR-26b controls neuronal differentiation by repressing its host transcript, ctdsp2.内含子 miR-26b 通过抑制其宿主转录本 ctdsp2 来控制神经元分化。
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Direct reprogramming of Sertoli cells into multipotent neural stem cells by defined factors.通过定义因子将支持细胞直接重编程为多能神经干细胞。
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诱导多能干细胞与直接重编程:治疗神经退行性疾病的新窗口。

Induced pluripotency and direct reprogramming: a new window for treatment of neurodegenerative diseases.

机构信息

State Key Laboratory of Brain and Cognitive Science, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Protein Cell. 2013 Jun;4(6):415-24. doi: 10.1007/s13238-013-2089-y. Epub 2013 May 20.

DOI:10.1007/s13238-013-2089-y
PMID:23686735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4875551/
Abstract

Human embryonic stem cells (hESCs) are pluripotent cells that have the ability of unlimited self-renewal and can be differentiated into different cell lineages, including neural stem (NS) cells. Diverse regulatory signaling pathways of neural stem cells differentiation have been discovered, and this will be of great benefit to uncover the mechanisms of neuronal differentiation in vivo and in vitro. However, the limitations of hESCs resource along with the religious and ethical concerns impede the progress of ESCs application. Therefore, the induced pluripotent stem cells (iPSCs) via somatic cell reprogramming have opened up another new territory for regenerative medicine. iPSCs now can be derived from a number of lineages of cells, and are able to differentiate into certain cell types, including neurons. Patient-specifi c iPSCs are being used in human neurodegenerative disease modeling and drug screening. Furthermore, with the development of somatic direct reprogramming or lineage reprogramming technique, a more effective approach for regenerative medicine could become a complement for iPSCs.

摘要

人类胚胎干细胞(hESCs)是多能细胞,具有无限自我更新的能力,并能分化为不同的细胞谱系,包括神经干细胞(NS)细胞。已经发现了神经干细胞分化的多种调节信号通路,这将有助于揭示体内和体外神经元分化的机制。然而,hESCs 资源的局限性以及宗教和伦理问题阻碍了 ESCs 应用的进展。因此,通过体细胞重编程产生的诱导多能干细胞(iPSCs)为再生医学开辟了另一个新领域。iPSCs 现在可以从多种细胞谱系中获得,并能分化为特定的细胞类型,包括神经元。患者特异性 iPSCs 正在用于人类神经退行性疾病建模和药物筛选。此外,随着体细胞直接重编程或谱系重编程技术的发展,一种更有效的再生医学方法可能成为 iPSCs 的补充。