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本文引用的文献

1
Human oocytes reprogram somatic cells to a pluripotent state.人类卵母细胞将体细胞重编程为多能状态。
Nature. 2011 Oct 5;478(7367):70-5. doi: 10.1038/nature10397.
2
Germline competence of mouse ES and iPS cell lines: Chimera technologies and genetic background.鼠胚胎干细胞和诱导多能干细胞系的种系嵌合能力:嵌合体技术和遗传背景。
World J Stem Cells. 2009 Dec 31;1(1):22-9. doi: 10.4252/wjsc.v1.i1.22.
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Immunogenicity of induced pluripotent stem cells.诱导多能干细胞的免疫原性。
Nature. 2011 May 13;474(7350):212-5. doi: 10.1038/nature10135.
4
Isolation and in vitro characterization of putative porcine embryonic stem cells from cloned embryos treated with trichostatin A.从经曲古抑菌素A处理的克隆胚胎中分离及体外鉴定假定的猪胚胎干细胞
Cell Reprogram. 2011 Jun;13(3):205-13. doi: 10.1089/cell.2010.0102. Epub 2011 May 7.
5
Mice cloned from induced pluripotent stem cells (iPSCs).由诱导多能干细胞(iPSCs)克隆的小鼠。
Biol Reprod. 2010 Aug 1;83(2):238-43. doi: 10.1095/biolreprod.110.084731. Epub 2010 Apr 28.
6
Hemangioblastic derivatives from human induced pluripotent stem cells exhibit limited expansion and early senescence.人诱导多能干细胞的血管母细胞衍生物表现出有限的扩增和早期衰老。
Stem Cells. 2010 Apr;28(4):704-12. doi: 10.1002/stem.321.
7
Generation of mouse embryonic stem cell lines from zona-free nuclear transfer embryos.从无透明带核移植胚胎中生成小鼠胚胎干细胞系。
Cell Reprogram. 2010 Feb;12(1):105-13. doi: 10.1089/cell.2009.0040.
8
Generation of human induced pluripotent stem cells by direct delivery of reprogramming proteins.通过直接递送重编程蛋白生成人类诱导多能干细胞。
Cell Stem Cell. 2009 Jun 5;4(6):472-6. doi: 10.1016/j.stem.2009.05.005. Epub 2009 May 28.
9
Virus-free induction of pluripotency and subsequent excision of reprogramming factors.无病毒诱导多能性及随后重编程因子的切除
Nature. 2009 Apr 9;458(7239):771-5. doi: 10.1038/nature07864. Epub 2009 Mar 1.
10
Human somatic cell nuclear transfer.人类体细胞核移植
Chin J Physiol. 2008 Aug 31;51(4):208-13.

核移植胚胎来源的小鼠胚胎干细胞的比较分析。第一部分:细胞特性

Comparative analysis of nuclear transfer embryo-derived mouse embryonic stem cells. Part I: cellular characterization.

作者信息

Kobolak Julianna, Mamo Solomon, Rungsiwiwut Ruttachuk, Ujhelly Olga, Csonka Erika, Hadlaczky Gyula, Dinnyes Andras

机构信息

Genetic Reprogramming Group, Agricultural Biotechnology Center, Gödöllő, Hungary.

出版信息

Cell Reprogram. 2012 Feb;14(1):56-67. doi: 10.1089/cell.2011.0056. Epub 2011 Dec 28.

DOI:10.1089/cell.2011.0056
PMID:22204592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3275094/
Abstract

Embryonic stem cells derived from nuclear transfer embryos (ntESCs) are particularly valuable for regenerative medicine, as they are a patient-specific and histocompatible cell source for the treatment of varying diseases. However, currently, little is known about their cellular and molecular profile. In the present study, in a mouse model different donor cell-derived ntESCs from various genetic backgrounds were compared with reference ESCs and analyzed comprehensively at the cellular level. A number of pluripotency marker genes were compared by flow cytometry and immunocytochemistry analysis. Significant differences at the protein level were observed for POU5F1, SOX2, FGF4, NANOG, and SSEA-1. However, such differences had no effect on in vitro cell differentiation and cell fate: derivatives of the three germ layers were detected in all ntESC lines. The neural and cardiac in vitro differentiation revealed minor differences between the cell lines, both at the mRNA and protein level. Karyotype analyses and cell growth studies did not reveal any significant variations. Despite some differences observed, the present study revealed that ntESC lines had similar differentiation competences compared to other ESCs. The results indicate that the observed differences may be related to the genotype rather than to the nuclear transfer technology.

摘要

源自核移植胚胎的胚胎干细胞(ntESCs)对再生医学尤为重要,因为它们是治疗各种疾病的患者特异性且组织相容性的细胞来源。然而,目前对于它们的细胞和分子特征了解甚少。在本研究中,在小鼠模型中,将来自不同遗传背景的不同供体细胞来源的ntESCs与对照胚胎干细胞进行比较,并在细胞水平上进行全面分析。通过流式细胞术和免疫细胞化学分析比较了多种多能性标记基因。在POU5F1、SOX2、FGF4、NANOG和SSEA-1的蛋白质水平上观察到显著差异。然而,这些差异对体外细胞分化和细胞命运没有影响:在所有ntESC系中均检测到三个胚层的衍生物。神经和心脏的体外分化在mRNA和蛋白质水平上均显示出细胞系之间的微小差异。核型分析和细胞生长研究未发现任何显著差异。尽管观察到一些差异,但本研究表明,与其他胚胎干细胞相比,ntESC系具有相似的分化能力。结果表明,观察到的差异可能与基因型而非核移植技术有关。