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Seven diverse human embryonic stem cell-derived chondrogenic clonal embryonic progenitor cell lines display site-specific cell fates

机译:七种不同的人类胚胎干细胞来源的成软骨克隆胚胎祖细胞系显示出特定于位点的细胞命运

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Aim: The transcriptomes of seven diverse clonal human embryonic progenitor cell lines with chondrogenic potential were compared with that of bone marrow-derived mesenchymal stem cells (MSCs). Materials & methods: The cell lines 4D20.8, 7PEND24, 7SMOO32, E15, MEL2, SK11 and SM30 were compared with MSCs using immunohistochemical methods, gene expression microarrays and quantitative real-time PCR. Results: In the undifferentiated progenitor state, each line displayed unique combinations of site-specific markers, including AJAP1, ALDH1A2, BMP5, BARX1, HAND2, HOXB2, LHX1, LHX8, PITX1, TBX15 and ZIC2, but none of the lines expressed the MSC marker CD74. The lines showed diverse responses when differentiated in the presence of combinations of TGF-β3, BMP2, 4, 6 and 7 and GDF5, with the lines 4D20.8, SK11, SM30 and MEL2 showing osteogenic markers in some differentiation conditions. The line 7PEND24 showed evidence of regenerating articular cartilage and, in some conditions, markers of tendon differentiation. Conclusion: The scalability of site-specific clonal human embryonic stem cell-derived embryonic progenitor cell lines may provide novel models for the study of differentiation and methods for preparing purified and identified cells types for use in therapy. Original submitted 16 October 2012; Revised submitted 22 November 2012; Published online 18 December 201.
机译:目的:比较7种具有软骨形成潜力的克隆人胚胎祖细胞系的转录组与骨髓源间充质干细胞(MSC)的转录组。材料与方法:使用免疫组织化学方法,基因表达微阵列和定量实时PCR,将细胞系4D20.8、7PEND24、7SMOO32,E15,MEL2,SK11和SM30与MSC进行比较。结果:在未分化的祖细胞状态下,每条品系均显示独特的位点特异性标记组合,包括AJAP1,ALDH1A2,BMP5,BARX1,HAND2,HOXB2,LHX1,LHX8,PITX1,TBX15和ZIC2,但均未表达MSC标记CD74。当在TGF-β3,BMP2、4、6和7和GDF5的​​组合存在下分化时,品系显示出不同的响应,而在某些分化条件下,品系4D20.8,SK11,SM30和MEL2显示出成骨标记。 7PEND24线显示出关节软骨再生的证据,在某些情况下还显示了腱分化的标志。结论:位点特异性克隆人胚胎干细胞衍生的胚胎祖细胞系的可扩展性可能为分化研究和制备用于治疗的纯化和鉴定细胞类型的方法提供新模型。原件于2012年10月16日提交; 2012年11月22日提交的修订本;在线发布于201年12月18日。

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