胎肝细胞提取物促进人胚胎干细胞的造血分化。

Yu-Xiao Liu, Lei Ji, Wen Yue, Zhi-Feng Yan, Jing Wang, Jia-Fei Xi, Rui Zhang, Xue Nan, Ci-Xian Bai, Lin Chen, Yun-Fang Wang, Xue-Tao Pei
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引用次数: 11

摘要

在这里,我们现在开发了一种新的诱导系统,通过人胎儿肝组织细胞提取物(hFLT)的处理,促进人类干细胞(hESCs)向造血谱系的分化。将从人H1胚胎干细胞获得的胚状体(EBs)分别暴露于缓冲液、hFLT细胞提取物、加热hFLT细胞提取物和人肝细胞系lo2细胞提取物中。然后,采用实时RT-PCR和菌落形成实验对不同组EBs的特征进行表征。结果表明,hFLT细胞提取物能激活造血基因表达,提高造血祖细胞发育能力。然后,我们将hFLT提取物处理过的hEBs在hFLSCs(人胎肝基质细胞)饲养器上共培养,使其分化为造血细胞。作为对照,未经处理的heb在hFLSCs饲养器上与细胞因子共培养。通过流式细胞术、Wright-Giemsa染色和集落形成实验表征了hEBs诱导细胞的特征。结果表明,hFLT细胞提取物能够诱导hEBs成为造血细胞,并与hFLSCs喂料剂结合可显著促进hESCs的造血分化。该方法为hESCs造血诱导所需细胞因子的替代提供了一种新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cells extract from fetal liver promotes the hematopoietic differentiation of human embryonic stem cells.

Here, we have now developed a new inducing system to promote the differentiation of human stem cells (hESCs) toward hematopoietic lineages by the treatment with cells extract of human fetal liver tissue (hFLT). The embryoid bodies (EBs) obtained from human H1 embryonic stem cells were exposed to buffer, hFLT cells extract, heated hFLT cell extract, and cell extract of human liver cells lines-LO2. Then, the feature of EBs in different groups was characterized by real-time RT-PCR and colony-forming assays. The results showed the treatment by hFLT cells extract could activate the hematopoietic genes expression and improve the capacity for hematopoietic progenitor development of hEBs. After that, we cocultured hFLT extract treated hEBs on the hFLSCs (human fetal liver stromal cells) feeder to differentiate them into hematopoietic cells. As a control, untreated hEBs were cocultured on hFLSCs feeder with cytokines. The feature of induced cells from hEBs was characterized by flow cytometry, Wright-Giemsa staining, and colony-forming assays. The results demonstrated that hFLT cells extract was capable of inducing hEBs into hematopoietic cells and combing it with hFLSCs feeder could largely promote hematopoietic differentiation of hESCs. This method may supply a new way to substitute the cytokines required in hematopoietic induction of hESCs.

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