首页> 外文期刊>Journal of Stem Cells and Regenerative Medicine >Chondrogenic differentiation of murine and human induced pluripotent stem cells in vitro: challenges and differences in comparison to ES cells
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Chondrogenic differentiation of murine and human induced pluripotent stem cells in vitro: challenges and differences in comparison to ES cells

机译:小鼠和人诱导的多能干细胞的软骨分化:与ES细胞相比的挑战和差异

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Induced pluripotent stem (iPS) cells hold great promise for research and potential therapeutic applications but the question whether iPS cells actually represent an equivalent alternative to embryonic stem (ES) cells regarding its use as an in vitro model system of cell differentiation remains to be answered. Our data shows that there are remarkable differences with respect to the chondrogenic differentiation capacity as well as the expression of pluripotency markers between undifferentiated murine and human iPS and ES cells. Murine iPS and ES cells were cultured as cell aggregates, the so called embryoid bodies (EBs), by the hanging drop method. Both cell lines could be differentiated into chondrocytes but iPS cells were found to be significantly less efficient. Further, iPS cell aggregations were smaller and less stable compared to ES cell EBs. The differentiation of human iPS cells is posing a challenge as established methods failed to produce EBs. EB formation by fragmentation of cell colonies was inefficient and aggregates from single cell suspension disaggregated.
机译:诱导多能干(iPS)细胞在研究和潜在治疗应用方面具有广阔的前景,但就其用作体外细胞分化模型系统而言,iPS细胞是否实际上代表了胚胎干(ES)细胞的等效替代品这一问题尚待解答。我们的数据表明,未分化的鼠与人iPS和ES细胞之间的软骨分化能力以及多能性标志物的表达存在显着差异。通过悬滴法将小鼠iPS和ES细胞培养为细胞聚集体,即所谓的胚状体(EBs)。两种细胞系都可以分化为软骨细胞,但发现iPS细胞的效率明显较低。此外,与ES细胞EB相比,iPS细胞聚集体更小且稳定性更差。由于建立的方法无法产生EB,人类iPS细胞的分化面临挑战。通过细胞集落破碎形成的EB效率低下,并且来自单个细胞悬液的聚集体被分解。

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