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本文引用的文献

1
Embryonic stem cell-like cells established by culture of adult ovarian cells in mice.成年小鼠卵巢细胞培养建立的胚胎干细胞样细胞。
Fertil Steril. 2010 May 15;93(8):2594-601, 2601.e1-9. doi: 10.1016/j.fertnstert.2009.12.053. Epub 2010 Feb 26.
2
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.
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Differentiation potential of germ line stem cells derived from the postnatal mouse ovary.从出生后小鼠卵巢中分离的生殖细胞干细胞的分化潜能。
Differentiation. 2010 Mar;79(3):159-70. doi: 10.1016/j.diff.2010.01.001. Epub 2010 Feb 6.
4
Propagation of human spermatogonial stem cells in vitro.人精原干细胞的体外增殖
JAMA. 2009 Nov 18;302(19):2127-34. doi: 10.1001/jama.2009.1689.
5
piggyBac transposon/transposase system to generate CD19-specific T cells for the treatment of B-lineage malignancies.利用 piggyBac 转座子/转座酶系统生成针对 CD19 的 T 细胞用于治疗 B 细胞恶性肿瘤。
Hum Gene Ther. 2010 Apr;21(4):427-37. doi: 10.1089/hum.2009.114.
6
Generation of canine induced pluripotent stem cells by retroviral transduction and chemical inhibitors.通过逆转录病毒转导和化学抑制剂生成犬诱导多能干细胞。
Mol Reprod Dev. 2010 Jan;77(1):2. doi: 10.1002/mrd.21117.
7
Reprogramming of human fibroblasts to induced pluripotent stem cells under xeno-free conditions.人成纤维细胞在无动物血清条件下向诱导多能干细胞的重编程。
Stem Cells. 2010 Jan;28(1):36-44. doi: 10.1002/stem.248.
8
Non cell-autonomous reprogramming of adult ocular progenitors: generation of pluripotent stem cells without exogenous transcription factors.非细胞自主重编程成年眼祖细胞:在没有外源转录因子的情况下产生多能干细胞。
Stem Cells. 2009 Dec;27(12):3053-62. doi: 10.1002/stem.242.
9
Isolation, characterization, and culture of human spermatogonia.人精原细胞的分离、鉴定和培养。
Biol Reprod. 2010 Feb;82(2):363-72. doi: 10.1095/biolreprod.109.078550. Epub 2009 Oct 21.
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Generation of human-induced pluripotent stem cells in the absence of exogenous Sox2.在不存在外源 Sox2 的情况下生成人类诱导多能干细胞。
Stem Cells. 2009 Dec;27(12):2992-3000. doi: 10.1002/stem.240.

替代性多能干细胞来源:伦理和科学问题再探讨。

Alternative sources of pluripotent stem cells: ethical and scientific issues revisited.

机构信息

Department of Neurobiology and Anatomy, University of Utah School of Medicine, Salt Lake City, Utah 84132-3401, USA.

出版信息

Stem Cells Dev. 2010 Aug;19(8):1121-9. doi: 10.1089/scd.2009.0482.

DOI:10.1089/scd.2009.0482
PMID:20397928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3128309/
Abstract

Stem cell researchers in the United States continue to face an uncertain future, because of the changing federal guidelines governing this research, the restrictive patent situation surrounding the generation of new human embryonic stem cell lines, and the ethical divide over the use of embryos for research. In this commentary, we describe how recent advances in the derivation of induced pluripotent stem cells and the isolation of germ-line-derived pluripotent stem cells resolve a number of these uncertainties. The availability of patient-matched, pluripotent stem cells that can be obtained by ethically acceptable means provides important advantages for stem cell researchers, by both avoiding protracted ethical debates and giving U.S. researchers full access to federal funding. Thus, ethically uncompromised stem cells, such as those derived by direct reprogramming or from germ-cell precursors, are likely to yield important advances in stem cell research and move the field rapidly toward clinical applications.

摘要

美国的干细胞研究人员继续面临不确定的未来,这是因为联邦指导方针的变化,以及新的人类胚胎干细胞系生成方面的专利限制,还有对胚胎用于研究的伦理分歧。在这篇评论中,我们描述了诱导多能干细胞的最新进展以及生殖细胞衍生的多能干细胞的分离如何解决了许多这些不确定性。通过符合伦理要求的手段获得与患者匹配的多能干细胞,为干细胞研究人员提供了重要的优势,既避免了旷日持久的伦理争论,又使美国研究人员能够全面获得联邦资金。因此,通过直接重编程或生殖细胞前体获得的合乎伦理的干细胞,可能会推动干细胞研究取得重要进展,并使该领域迅速向临床应用推进。