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In VitroCulture-Induced Pluripotency of Human Spermatogonial Stem Cells

机译:体外培养人精原干细胞的多能性

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Unipotent spermatogonial stem cells (SSCs) can be transformed into ESC-like cells that exhibit pluripotencyin vitro. However, except for mouse models, their characterization and their origins have remained controversies in other models including humans. This controversy has arisen primarily from the lack of the direct induction of ESC-like cells from well-characterized SSCs. Thus, the aim of the present study was to find and characterize pluripotent human SSCs inin vitrocultures of characterized SSCs. Human testicular tissues were dissociated and plated onto gelatin/laminin-coated dishes to isolate SSCs. In the presence of growth factors SSCs formed multicellular clumps after 2–4 weeks of culture. At passages 1 and 5, the clumps were dissociated and were then analyzed using markers of pluripotent cells. The number of SSEA-4-positive cells was extremely low but increased gradually up to ~ 10% in the SSC clumps during culture. Most of the SSEA-4-negative cells expressed markers for SSCs, and some cells coexpressed markers of both pluripotent and germ cells. The pluripotent cells formed embryoid bodies and teratomas that contained derivatives of the three germ layers in SCID mice. These results suggest that the pluripotent cells present within the clumps were derived directly from SSCs duringin vitroculture.
机译:可以将单能精原干细胞(SSC)转化为在体外表现出多能性的ESC样细胞。但是,除了鼠标模型之外,它们的特征及其起源在包括人类在内的其他模型中仍然存在争议。引起这种争议的主要原因是缺乏从特征明确的SSC直接诱导ESC样细胞的能力。因此,本研究的目的是在具有特征的SSC的体外培养物中发现并表征多能人SSC。将人的睾丸组织解离并铺在明胶/粘蛋白包被的培养皿上以分离SSC。在存在生长因子的情况下,培养2至4周后,SSC会形成多细胞团块。在第1和5代,将团块解离,然后使用多能细胞标记进行分析。在培养过程中,SSC团块中SSEA-4阳性细胞的数量极少,但逐渐增加至〜10%。大多数SSEA-4-阴性细胞表达SSC的标志物,一些细胞共表达多能和生殖细胞的标志物。多能细胞形成胚状体和畸胎瘤,它们包含SCID小鼠中三个胚层的衍生物。这些结果表明,在体外培养期间,团块内存在的多能细胞直接来自SSC。

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