1Division of Pathology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
2Royan Institute for Stem Cell Biology, Tehran, Iran.
Stem Cells Dev. 2019 Jul 15;28(14):907-919. doi: 10.1089/scd.2019.0064.
Differentiation of stem cells to hepatocyte-like cells (HLCs) holds great promise for basic research, drug and toxicological investigations, and clinical applications. There are currently no protocols for the production of HLCs from stem cells, such as embryonic stem cells or induced pluripotent stem cells, that produce fully mature hepatocytes with a wide range of mature hepatic functions. This report describes a standard method to assess the maturation of stem cell-derived HLCs with a moderately high-throughput format, by analysing liver gene expression by quantitative RT-qPCR. This method also provides a robust data set of the expression of 62 genes expressed in normal liver, generated from 17 fetal and 25 mature human livers, so that investigators can quickly and easily compare the expression of these genes in their stem cell-derived HLCs with the values obtained in authentic fetal and mature human liver. The simple methods described in this study will provide a quick and accurate assessment of the efficacy of a differentiation protocol and will help guide the optimization of differentiation conditions.
干细胞向肝样细胞(HLC)的分化在基础研究、药物和毒理学研究以及临床应用方面具有广阔的前景。目前尚无从干细胞(如胚胎干细胞或诱导多能干细胞)产生具有广泛成熟肝功能的完全成熟肝细胞的方案。本报告描述了一种使用定量 RT-qPCR 分析肝基因表达来评估干细胞来源的 HLC 成熟度的标准方法。该方法还提供了一组来自 17 个胎儿和 25 个成人肝脏的 62 个正常肝脏表达基因的稳健数据集,使研究人员能够快速轻松地比较其干细胞来源的 HLC 中这些基因的表达与从真实胎儿和成人肝脏中获得的值。本研究中描述的简单方法将为分化方案的效果提供快速准确的评估,并有助于指导分化条件的优化。