首页> 美国卫生研究院文献>Cellular Reprogramming >ROCK Inhibition Facilitates the Generation of Human-Induced Pluripotent Stem Cells in a Defined Feeder- and Serum-Free System
【2h】

ROCK Inhibition Facilitates the Generation of Human-Induced Pluripotent Stem Cells in a Defined Feeder- and Serum-Free System

机译:ROCK抑制作用在定义的无饲养层和无血清的系统中促进人类诱导的多能干细胞的产生

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Human-induced pluripotent stem cells (iPSCs) generated from human adult somatic cells through reprogramming hold great promises for future regenerative medicine. However, exposure of human iPSCs to animal feeder and serum in the process of their generation and maintenance imposes risk of transmitting animal pathogens to human subjects, thus hindering the potential therapeutic applications. Here, we report the successful generation of human iPSCs in a feeder-independent culture system with defined factors. Two stable human iPSC lines were established from primary human dermal fibroblasts of two healthy volunteers. These human iPSCs expressed a panel of pluripotency markers including stage-specific embryonic antigen (SSEA)-4, tumor-rejection antigen (TRA)-1-60, TRA-1-81, and alkaline phosphatase, while maintaining normal karyotypes and the exogenous reprogramming factors being silenced. In addition, these human iPSCs can differentiate along lineages representative of the three embryonic germ layers upon formation of embryoid bodies, indicating their pluripotency. Furthermore, subcutaneous transplantation of these cells into immunodeficient mice resulted in teratoma formation in 6 to 8 weeks. Our findings are an important step toward generating patient-specific iPSCs in a more clinically compliant manner by eliminating the need of animal feeder cells and animal serum.
机译:通过重编程从人成年体细胞产生的人诱导多能干细胞(iPSC)为未来的再生医学大有希望。但是,人iPSC在其产生和维持过程中暴露于动物饲养层和血清会增加将动物病原体传播给人类受试者的风险,从而阻碍了潜在的治疗应用。在这里,我们报告了人类iPSC在具有定义因素的与饲养者无关的培养系统中的成功产生。从两名健康志愿者的原代人皮肤成纤维细胞建立了两个稳定的人iPSC系。这些人iPSC表达了一组多能性标志物,包括阶段特异性胚胎抗原(SSEA)-4,肿瘤排斥抗原(TRA)-1-60,TRA-1-81和碱性磷酸酶,同时保持了正常的核型和外源性重编程因素被沉默。此外,这些人iPSC可以在形成胚状体时沿代表三个胚芽层的谱系分化,表明它们的全能性。此外,将这些细胞皮下移植到免疫缺陷小鼠中会在6至8周内形成畸胎瘤。我们的发现是通过消除对动物饲养细胞和动物血清的需求,以更符合临床要求的方式生产针对患者的iPSC的重要一步。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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