Bhattacharya Bhaskar, Miura Takumi, Brandenberger Ralph, Mejido Josef, Luo Yongquan, Yang Amy X, Joshi Bharat H, Ginis Irene, Thies R Scott, Amit Michal, Lyons Ian, Condie Brian G, Itskovitz-Eldor Joseph, Rao Mahendra S, Puri Raj K
Laboratory of Molecular Tumor Biology, Division of Cellular and Gene Therapies, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892, USA.
Blood. 2004 Apr 15;103(8):2956-64. doi: 10.1182/blood-2003-09-3314. Epub 2003 Dec 30.
Human embryonic stem (huES) cells have the ability to differentiate into a variety of cell lineages and potentially provide a source of differentiated cells for many therapeutic uses. However, little is known about the mechanism of differentiation of huES cells and factors regulating cell development. We have used high-quality microarrays containing 16 659 seventy-base pair oligonucleotides to examine gene expression in 6 of the 11 available huES cell lines. Expression was compared against pooled RNA from multiple tissues (universal RNA) and genes enriched in huES cells were identified. All 6 cell lines expressed multiple markers of the undifferentiated state and shared significant homology in gene expression (overall similarity coefficient > 0.85).A common subset of 92 genes was identified that included Nanog, GTCM-1, connexin 43 (GJA1), oct-4, and TDGF1 (cripto). Gene expression was confirmed by a variety of techniques including comparison with databases, reverse transcriptase-polymerase chain reaction, focused cDNA microarrays, and immunocytochemistry. Comparison with published "stemness" genes revealed a limited overlap, suggesting little similarity with other stem cell populations. Several novel ES cell-specific expressed sequence tags were identified and mapped to the human genome. These results represent the first detailed characterization of undifferentiated huES cells and provide a unique set of markers to profile and better understand the biology of huES cells.
人胚胎干细胞(huES细胞)有能力分化为多种细胞谱系,并有可能为许多治疗用途提供分化细胞的来源。然而,对于huES细胞的分化机制以及调节细胞发育的因子了解甚少。我们使用了包含16659个70碱基对寡核苷酸的高质量微阵列,来检测11个可用huES细胞系中6个细胞系的基因表达。将其表达与来自多个组织的混合RNA(通用RNA)进行比较,从而鉴定出在huES细胞中富集的基因。所有6个细胞系均表达了未分化状态的多个标志物,并且在基因表达上具有显著的同源性(总体相似系数>0.85)。鉴定出了一个包含Nanog、GTCM-1、连接蛋白43(GJA1)、八聚体结合转录因子4(oct-4)和TDGF1(cripto)的92个基因的共同子集。通过多种技术证实了基因表达,包括与数据库比较、逆转录-聚合酶链反应、聚焦cDNA微阵列和免疫细胞化学。与已发表的“干性”基因比较显示重叠有限,表明与其他干细胞群体几乎没有相似性。鉴定出了几个新的ES细胞特异性表达序列标签,并将其定位到人类基因组。这些结果代表了未分化huES细胞的首次详细特征描述,并提供了一组独特的标志物来描绘和更好地理解huES细胞的生物学特性。