State Key Lab of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences, Tianjin, China.
Stem Cell Rev Rep. 2015 Apr;11(2):219-27. doi: 10.1007/s12015-014-9582-4.
The differentiated cell lineages from human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs) have shown their potential in regenerative medicine. However, the functional and transcriptional microRNA (miRNA) expression pattern during endothelial differentiation has yet to be characterized.
In this study, hESCs and hiPSCs were differentiated into endothelial cells (ECs). Then the endothelial-related gene profiling and miRNA profiling of hiPSCs, hESCs, hiPSCs derived endothelial cells (hiPSC-ECs), hESC derived endothelial cells (hESC-ECs) and human umbilical vein endothelial cells (HUVECs) were compared using RT-PCR Array. The data was analyzed using the data analysis system on QIAGEN's website.
Our analysis demonstrated that the endothelial differentiation was triggered after EB formation and the EC-associated genes were up-regulated swiftly in both hESC-EBs and hiPSC-EBs; hiPSC-ECs and hESC-ECs had the similar EC-associated gene expression patterns. Moreover, we report here the first miRNA profiling study of hiPSC-ECs. Analyzing 376 unique miRNAs, we have identified several interesting miRNAs, including miR-20a, miR-20b, miR-222, miR-210, which have been previously reported to be involved in endothelial differentiation and show surprising expression patterns across our samples. We also identified novel miRNAs, such as miR-125a-5p, miR-149, miR-296-5p, miR-100, miR-27b, miR-181a and miR-137, which were up-regulated in both hiPSC-ECs and hESC-ECs during endothelial differentiation.
hiPSC-ECs and hESC-ECs exhibited a high degree of similarity with HUVECs in EC-associated genes expression. And the miRNA profiling analysis revealed significant differences between hiPSCs and hESCs, but a high degree of similarity between hiPSC-ECs and hESC-ECs.
人类胚胎干细胞(hESC)和人类诱导多能干细胞(hiPSC)分化的细胞谱系在再生医学中显示出了它们的潜力。然而,内皮细胞分化过程中的功能和转录microRNA(miRNA)表达模式尚未得到描述。
在这项研究中,hESC 和 hiPSC 被分化为内皮细胞(EC)。然后,使用 RT-PCR 阵列比较 hiPSC、hESC、hiPSC 衍生的内皮细胞(hiPSC-EC)、hESC 衍生的内皮细胞(hESC-EC)和人脐静脉内皮细胞(HUVEC)的内皮相关基因谱和 miRNA 谱。使用 QIAGEN 网站上的数据分析系统对数据进行分析。
我们的分析表明,内皮分化是在 EB 形成后触发的,EC 相关基因在 hESC-EB 和 hiPSC-EB 中迅速上调;hiPSC-EC 和 hESC-EC 具有相似的 EC 相关基因表达模式。此外,我们在这里报告了 hiPSC-EC 的第一个 miRNA 分析研究。分析 376 个独特的 miRNA,我们发现了一些有趣的 miRNA,包括 miR-20a、miR-20b、miR-222、miR-210,它们之前被报道参与内皮分化,并在我们的样本中表现出惊人的表达模式。我们还鉴定了一些新的 miRNA,如 miR-125a-5p、miR-149、miR-296-5p、miR-100、miR-27b、miR-181a 和 miR-137,它们在 hiPSC-EC 和 hESC-EC 内皮分化过程中均上调。
hiPSC-EC 和 hESC-EC 在 EC 相关基因表达方面与 HUVEC 高度相似。miRNA 分析揭示了 hiPSC 和 hESC 之间的显著差异,但 hiPSC-EC 和 hESC-EC 之间具有高度的相似性。