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首页> 外文期刊>Animal Cells and Systems >Reprogramming of spermatogonial stem cells into pluripotent stem cells in the spheroidal state
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Reprogramming of spermatogonial stem cells into pluripotent stem cells in the spheroidal state

机译:将精原干细胞重编程为球状多能干细胞

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ABSTRACTSpermatogonial stem cells (SSCs) are unipotent adult stem cells, capable of differentiating into sperm cells. SSCs can be cultured in vitro for a long time. SSCs expressing Oct4, a pluripotency marker, and are the only adult cells which pluripotency can be induced under defined culture conditions. However, because 2D culture imposes limitations in cell junction formation, cell shape, metabolism, response to stimuli, and cell interface with medium, mechanistic studies on reprogramming of SSCs using feeder cells still have many challenges. Recent studies have shown that a culture system using a bio-matrix can be used in long-term feeder-free SSCs culture and for induction of pluripotency in SSCs. However, the bio-matrix cannot be the optimal micro-environment in mechanistic studies because it creates a physical barrier to growth factors and other signaling molecules. To overcome this effect of the matrix, we reprogrammed SSCs into pluripotent ESC-like cells, so-called germline-derived pluripotent stem cells (gPSCs) by using a 3D scaffold, in which cells are less responsive to external stimuli than in 2D cultures. Thus, we confirm the possibility of SSC reprogramming in the spheroidal state and suggest the utility of 3D scaffolds as a tool for studying the mechanism of SSC reprogramming into gPSCs without a bio-matrix.
机译:精原干细胞(SSCs)是单能成年干细胞,能够分化成精子细胞。 SSC可以在体外长时间培养。表达Oct4(一种多能性标志物)的SSC是在确定的培养条件下可诱导多能性的唯一成年细胞。但是,由于2D培养在细胞连接形成,细胞形状,代谢,对刺激的应答以及细胞与培养基的接触方面施加了限制,因此使用饲养细胞对SSC重新编程的机理研究仍然面临许多挑战。最近的研究表明,使用生物基质的培养系统可用于长期无饲养者的SSC培养,并在SSC中诱导多能性。但是,生物基质不能成为机械研究中的最佳微环境,因为它对生长因子和其他信号分子产生了物理障碍。为了克服基质的这种作用,我们通过使用3D支架将SSC重新编程为多能ESC样细胞,即所谓的种系衍生的多能干细胞(gPSC),其中3D支架的细胞比2D培养的细胞对外部刺激的反应性更低。因此,我们确认了球状状态下SSC重编程的可能性,并建议使用3D支架作为研究SSC重编程成gPSCs而无需生物基质的机制的工具。

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