首页> 美国卫生研究院文献>Stem Cells International >Comparison of Gene Expression in Human Embryonic Stem Cells hESC-Derived Mesenchymal Stem Cells and Human Mesenchymal Stem Cells
【2h】

Comparison of Gene Expression in Human Embryonic Stem Cells hESC-Derived Mesenchymal Stem Cells and Human Mesenchymal Stem Cells

机译:人类胚胎干细胞中基因表达的比较 hESC来源的间充质干细胞和人间充质干 细胞

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

We present a strategy to identify developmental/differentiation and plasma membrane marker genes of the most primitive human Mesenchymal Stem Cells (hMSCs). Using sensitive and quantitative TaqMan Low Density Arrays (TLDA) methodology, we compared the expression of 381 genes in human Embryonic Stem Cells (hESCs), hESC-derived MSCs (hES-MSCs), and hMSCs. Analysis of differentiation genes indicated that hES-MSCs express the sarcomeric muscle lineage in addition to the classical mesenchymal lineages, suggesting they are more primitive than hMSCs. Transcript analysis of membrane antigens suggests that IL1R1low, BMPR1Blow, FLT4low, LRRC32low, and CD34 may be good candidates for the detection and isolation of the most primitive hMSCs. The expression in hMSCs of cytokine genes, such as IL6, IL8, or FLT3LG, without expression of the corresponding receptor, suggests a role for these cytokines in the paracrine control of stem cell niches. Our database may be shared with other laboratories in order to explore the considerable clinical potential of hES-MSCs, which appear to represent an intermediate developmental stage between hESCs and hMSCs.
机译:我们提出了一种战略,以确定最原始的人类间充质干细胞(hMSCs)的发育/分化和质膜标记基因。使用敏感和定量的TaqMan低密度阵列(TLDA)方法,我们比较了381个基因在人类胚胎干细胞(hESCs),hESC衍生的MSC(hES-MSC)和hMSC中的表达。分化基因的分析表明,hES-MSC除经典的间充质谱系外还表达肌节肌谱系,表明它们比hMSC更为原始。膜抗原的转录本分析表明,IL1R1 low ,BMPR1B low ,FLT4 low ,LRRC32 low 和CD34是检测和隔离最原始hMSC的良好候选者。细胞因子基因(例如IL6,IL8或FLT3LG)在hMSC中的表达而没有相应受体的表达,提示这些细胞因子在干细胞壁ni的旁分泌控制中起作用。我们的数据库可能与其他实验室共享,以探索hES-MSC的巨大临床潜力,这似乎代表了hESC和hMSC之间的中间发育阶段。

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