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Urothelial differentiation of human amniotic fluid stem cells by urothelium specific conditioned medium

机译:尿路上皮特异性条件培养基对人羊水干细胞的尿道分化

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摘要

Human amniotic fluid stem cells (HAFSCs) have a high proliferative capacity and a good differentiation potential, and may thus be suitable for regenerative medicine. To date, urothelial differentiation mechanisms of HAFSCs are poorly understood. We have investigated the urothelial differentiation potential of HAFSCs so that they can be therapeutically applied to cure defective diseases of bladder. To induce the stem cell differentiation, HAFSCs were cultured in a bladder cancer-derived conditioned medium. After 2 weeks of culture, HAFSCs began to express the urothelial lineage-specific markers (UPII, CK8 and FGF10). Meanwhile, pluripotency markers (Oct-4, Sox-2 and Nanog) were downregulated at both RNA and protein levels in the differentiated HAFSCs. Immunocytochemistry data revealed that differentiated HAFSCs expressed urothelial markers of UPII and CK8. We have screened the receptor tyrosine kinase arrays with the differentiated HAFSCs. The screening showed that MuSK, Tie-1 and EphA4 receptor tyrosine kinases were upregulated, whereas EphA7 and FGF R1 kinases were downregulated in HAFSCs. The data suggest that HAFSCs can be an important urothelium cell source, which can be use for urinary tract engineering.
机译:人羊水干细胞(HAFSC)具有高增殖能力和良好的分化潜能,因此可能适合于再生医学。迄今为止,对HAFSC的尿路上皮分化机制了解甚少。我们已经研究了HAFSCs的尿路上皮分化潜能,以便可以将其用于治疗膀胱缺陷疾病。为了诱导干细胞分化,在膀胱癌衍生的条件培养基中培养HAFSC。培养2周后,HAFSC开始表达尿路上皮谱系特异性标记(UPII,CK8和FGF10)。同时,在分化的HAFSCs中,RNA和蛋白质水平的多能性标志物(Oct-4,Sox-2和Nanog)均被下调。免疫细胞化学数据显示,分化的HAFSCs表达UPII和CK8的尿路上皮标记。我们已经用分化的HAFSCs筛选了受体酪氨酸激酶阵列。筛选显示,HAFSC中的MuSK,Tie-1和EphA4受体酪氨酸激酶被上调,而EphA7和FGF R1激酶被下调。数据表明,HAFSC可能是重要的尿道上皮细胞来源,可用于泌尿道工程。

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