...
首页> 外文期刊>The Journal of Reproduction and Development >Development of culture conditions for the isolation of pluripotent porcine embryonal outgrowths from in vitro produced and in vivo derived embryos.
【24h】

Development of culture conditions for the isolation of pluripotent porcine embryonal outgrowths from in vitro produced and in vivo derived embryos.

机译:从体外产生的和体内衍生的胚胎中分离多能性猪胚胎生长产物的培养条件的发展。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

In the present study we examined the effect of culture media and protein source on the formation of pluripotent primary outgrowths from in vitro produced and in vivo derived porcine embryos as the first step towards the isolation of embryonic stem cells (ESCs). To do this we compared high glucose Dulbeccos Modified Eagles Medium (DMEM) with Minimal Essential Alpha Medium (MEM) both supplemented with fetal bovine serum (FBS) or serum replacement (SR) in a 2 x 2 factorial design. Culture in DMEM or MEM supplemented with 10% SR resulted in the establishment of homogenous populations of cells which expressed Oct 4 and Nanog. In contrast culture in either media with FBS resulted in the formation of embryonal outgrowths composed entirely of differentiated cells or a mixture of differentiated cells and putative ESCs which grew poorly and could not be passaged. Using MEM medium containing 10% SR and culturing in 5% oxygen, putative ESC lines were isolated from in vitro and in vivo derived embryos at efficiencies of 2 and 10% respectively.
机译:在本研究中,我们研究了培养基和蛋白质来源对从体外产生的和体内衍生的猪胚胎多能性初级产物形成的影响,这是分离胚胎干细胞(ESC)的第一步。为此,我们在2 x 2因子设计中比较了高葡萄糖Dulbeccos改良的Eagles培养基(DMEM)与最小必需Alpha培养基(MEM)两者均补充了胎牛血清(FBS)或血清替代品(SR)。在DMEM或补充有10%SR的MEM中进行培养导致建立了表达Oct4和Nanog的同质细胞群体。相比之下,在任何一种含有FBS的培养基中进行培养都会导致胚胎生长的产物完全由分化的细胞组成,或者由分化的细胞与推定的ESC混合而成,它们生长缓慢且无法传代。使用含有10%SR的MEM培养基并在5%氧气中培养,从体外和体内衍生的胚胎中分别以2%和10%的效率分离出推定的ESC品系。

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