首页> 外文期刊>Tissue and Cell >Culture of mouse spermatogonial stem cells
【24h】

Culture of mouse spermatogonial stem cells

机译:小鼠精原干细胞的培养

获取原文
获取原文并翻译 | 示例
       

摘要

It has previously been thought that germ cells survive for only a brief period in culture. An accurate assessment of the presence of spermatogonial stem cells in any cell population has recently become possible with development of the spermatogonialtransplantation technique. Using this technique, it was shown that mouse spermatogonial stem cells can be maintained in culture for approximately 4 months and can produce spermatozoa following transplantation to the seminiferous tubules of an appropriate recipient. Extensive areas of cultured donor cell-derived spermatogenesis were generated in the host, and mature spermatozoa were produced. Cultivation of the testis cells on STO feeder cells improved stem cell survival.
机译:以前认为生殖细胞只能在培养中存活很短的时间。随着精原细胞移植技术的发展,对任何细胞群体中精原干细胞的存在进行精确评估成为可能。使用该技术显示,小鼠精原干细胞可以在培养物中维持约4个月,并且在移植到合适受体的生精小管后可以产生精子。在宿主中产生了广泛的培养供体细胞衍生的精子发生区域,并产生了成熟的精子。在STO饲养细胞上培养睾丸细胞可改善干细胞存活率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号