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本文引用的文献

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Local Genome Topology Can Exhibit an Incompletely Rewired 3D-Folding State during Somatic Cell Reprogramming.局部基因组拓扑结构在体细胞重编程过程中可能呈现出一种未完全重新布线的三维折叠状态。
Cell Stem Cell. 2016 May 5;18(5):611-24. doi: 10.1016/j.stem.2016.04.004.
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Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups.人类诱导多能干细胞衍生视杯遗传性失明潜在机制的识别与校正
Cell Stem Cell. 2016 Jun 2;18(6):769-781. doi: 10.1016/j.stem.2016.03.021. Epub 2016 Apr 14.
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Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs.年龄相关的体细胞线粒体 DNA 突变在成人来源的人类诱导多能干细胞中的积累。
Cell Stem Cell. 2016 May 5;18(5):625-36. doi: 10.1016/j.stem.2016.02.005. Epub 2016 Apr 14.
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Genome Editing of Lineage Determinants in Human Pluripotent Stem Cells Reveals Mechanisms of Pancreatic Development and Diabetes.人类多能干细胞中谱系决定因子的基因组编辑揭示胰腺发育和糖尿病的机制
Cell Stem Cell. 2016 Jun 2;18(6):755-768. doi: 10.1016/j.stem.2016.03.015. Epub 2016 Apr 28.
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Chemical Control of Grafted Human PSC-Derived Neurons in a Mouse Model of Parkinson's Disease.帕金森病小鼠模型中移植的人多能干细胞衍生神经元的化学调控
Cell Stem Cell. 2016 Jun 2;18(6):817-826. doi: 10.1016/j.stem.2016.03.014. Epub 2016 Apr 28.
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2D and 3D Stem Cell Models of Primate Cortical Development Identify Species-Specific Differences in Progenitor Behavior Contributing to Brain Size.灵长类皮质发育的二维和三维干细胞模型揭示了祖细胞行为中导致脑容量差异的物种特异性差异。
Cell Stem Cell. 2016 Apr 7;18(4):467-80. doi: 10.1016/j.stem.2016.03.003. Epub 2016 Mar 31.
7
MLL1 Inhibition Reprograms Epiblast Stem Cells to Naive Pluripotency.MLL1抑制将上胚层干细胞重编程为原始多能性。
Cell Stem Cell. 2016 Apr 7;18(4):481-94. doi: 10.1016/j.stem.2016.02.004. Epub 2016 Mar 17.
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Divergent lncRNAs Regulate Gene Expression and Lineage Differentiation in Pluripotent Cells.差异长非编码 RNA 调控多能干细胞中的基因表达和谱系分化。
Cell Stem Cell. 2016 May 5;18(5):637-52. doi: 10.1016/j.stem.2016.01.024. Epub 2016 Mar 17.
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Stepwise Differentiation of Retinal Ganglion Cells from Human Pluripotent Stem Cells Enables Analysis of Glaucomatous Neurodegeneration.从人类多能干细胞逐步分化视网膜神经节细胞有助于青光眼神经退行性变的分析。
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10
CRISPR Interference Efficiently Induces Specific and Reversible Gene Silencing in Human iPSCs.CRISPR干扰可有效诱导人诱导多能干细胞中特定且可逆的基因沉默。
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学术界中诱导多能干细胞明确且无动物成分培养的停滞性适应

The Stagnant Adaptation of Defined and Xeno-Free Culture of iPSCs in Academia.

作者信息

Vecchi Joseph T, Wakatsuki Tetsuro

机构信息

InvivoSciences, Inc., USA.

出版信息

Arch Stem Cell Res. 2015;3(1). Epub 2016 Nov 8.

PMID:29333534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5766037/
Abstract

Pluripotent Stem Cells were originally derived and cultured using a feeder layer of cells. Movements have been undertaken to transition from this method to one more defined, high-throughput, and without xenogenic factors. Tremendous research has been done in this area and many products have been developed, however, based on our analysis of recent publications in stem cell related journals many in academia are still using older methods like a feeder layer. In this short communication, we discuss the feasibility of transitioning to defined, xeno-free methods, how a standardized method could improve the field and industry, and that a study bringing together multiple institutions comparing culture methods could be done to evaluate the efficacy of these new methods.

摘要

多能干细胞最初是使用饲养层细胞进行衍生和培养的。目前已开展了相关行动,旨在从这种方法过渡到一种定义更明确、高通量且无外源因素的方法。该领域已开展了大量研究并开发了许多产品,然而,基于我们对干细胞相关期刊近期出版物的分析,学术界许多人仍在使用诸如饲养层等较老的方法。在这篇简短的通讯中,我们讨论了过渡到定义明确的无外源方法的可行性、标准化方法如何能改进该领域和行业,以及可以开展一项汇集多个机构比较培养方法的研究,以评估这些新方法的有效性。