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Highly efficient reprogramming to pluripotency and directed differentiation of human cells with synthetic modified mRNA.利用合成修饰 mRNA 高效重编程人类细胞为多能性干细胞并进行定向分化。
Cell Stem Cell. 2010 Nov 5;7(5):618-30. doi: 10.1016/j.stem.2010.08.012. Epub 2010 Sep 30.
2
Safety paradigm: genetic evaluation of therapeutic grade human embryonic stem cells.安全模式:治疗级人类胚胎干细胞的基因评估。
J R Soc Interface. 2010 Dec 6;7 Suppl 6(Suppl 6):S677-88. doi: 10.1098/rsif.2010.0343.focus. Epub 2010 Sep 8.
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Epigenetic memory in induced pluripotent stem cells.诱导多能干细胞中的表观遗传记忆。
Nature. 2010 Sep 16;467(7313):285-90. doi: 10.1038/nature09342.
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Stem cells: roadmap to the clinic.干细胞:通往临床的路线图。
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Reprogramming towards pluripotency requires AID-dependent DNA demethylation.重编程为多能性需要 AID 依赖性的 DNA 去甲基化。
Nature. 2010 Feb 25;463(7284):1042-7. doi: 10.1038/nature08752.
6
Technical challenges in using human induced pluripotent stem cells to model disease.使用人类诱导多能干细胞进行疾病建模的技术挑战。
Cell Stem Cell. 2009 Dec 4;5(6):584-95. doi: 10.1016/j.stem.2009.11.009.
7
Mitochondrial gene replacement in primate offspring and embryonic stem cells.灵长类动物后代及胚胎干细胞中的线粒体基因替换
Nature. 2009 Sep 17;461(7262):367-72. doi: 10.1038/nature08368. Epub 2009 Aug 26.
8
Diversity in public views toward stem cell sources and policies.公众对干细胞来源和政策的看法存在差异。
Stem Cell Rev Rep. 2009 Jun;5(2):102-7. doi: 10.1007/s12015-009-9063-3. Epub 2009 Apr 22.
9
Generation of induced pluripotent stem cells using recombinant proteins.利用重组蛋白生成诱导多能干细胞。
Cell Stem Cell. 2009 May 8;4(5):381-4. doi: 10.1016/j.stem.2009.04.005. Epub 2009 Apr 23.
10
Inter-species embryos and human clones: issues of free movement and gestation.跨物种胚胎与人类克隆:自由移动与妊娠问题。
Eur J Health Law. 2009 Mar;16(1):69-79. doi: 10.1163/157180908x378409.

人多能干细胞诱导中的技术挑战。

Technical challenges in the derivation of human pluripotent cells.

机构信息

Embryo Technology and Stem Cell Research Center, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, 111 University Avenue, Nakhon Ratchasima 30000, Thailand.

出版信息

Stem Cells Int. 2011;2011:907961. doi: 10.4061/2011/907961. Epub 2011 Jun 19.

DOI:10.4061/2011/907961
PMID:21776284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3138062/
Abstract

It has long been discovered that human pluripotent cells could be isolated from the blastocyst state of embryos and called human embryonic stem cells (ESCs). These cells can be adapted and propagated indefinitely in culture in an undifferentiated manner as well as differentiated into cell representing the three major germ layers: endoderm, mesoderm, and ectoderm. However, the derivation of human pluripotent cells from donated embryos is limited and restricted by ethical concerns. Therefore, various approaches have been explored and proved their success. Human pluripotent cells can also be derived experimentally by the nuclear reprogramming of somatic cells. These techniques include somatic cell nuclear transfer (SCNT), cell fusion and overexpression of pluripotent genes. In this paper, we discuss the technical challenges of these approaches for nuclear reprogramming, involving their advantages and limitations. We will also highlight the possible applications of these techniques in the study of stem cell biology.

摘要

长期以来,人们已经发现可以从胚胎的囊胚状态中分离出人类多能细胞,并将其称为人类胚胎干细胞(ESCs)。这些细胞可以在培养中以未分化的方式适应和无限繁殖,并分化为代表三个主要胚层的细胞:内胚层、中胚层和外胚层。然而,从捐赠的胚胎中获得人类多能细胞受到伦理问题的限制。因此,人们已经探索了各种方法,并证明了它们的成功。人类多能细胞也可以通过体细胞的核重编程实验获得。这些技术包括体细胞核移植(SCNT)、细胞融合和多能基因的过表达。在本文中,我们讨论了这些核重编程方法的技术挑战,包括它们的优点和局限性。我们还将重点介绍这些技术在干细胞生物学研究中的可能应用。