Lysy Philippe A, Smets Françoise, Najimi Mustapha, Sokal Etienne M
HPED Department, PEDI Unit, Université Catholique de Louvain, Cliniques Universitaires Saint Luc, Brussels, Belgium.
Differentiation. 2008 Dec;76(10):1057-67. doi: 10.1111/j.1432-0436.2008.00287.x. Epub 2008 Jun 13.
The current majority of protocols for hepatocyte differentiation of mesenchymal stem cells (MSCs) are conducted using oncostatin M (OSM) as an inducer of hepatocyte-like maturation. As leukemia inhibitory factor (LIF) and OSM share similar signaling pathways, we examined whether LIF could play a role in the hepatocyte differentiation process. A differentiation protocol was designed using LIF as a maturation cytokine and this was compared with standard and control protocols applied to human MSCs of bone marrow origin. We observed that mesenchymal-derived hepatocyte-like cells (MDHLCs) acquired similar morphological changes when exposed to LIF or to OSM. Using protein and gene expression assays, we noticed a comparable hepatic marker expression in both differentiation conditions. Furthermore, LIF and OSM allowed the acquisition of equivalent levels of hepatocyte-like functionality as attested by evaluation of urea secretion and glycogen deposition. However, no increase in the expression of hepatocyte-like features could be observed in MDHLCs after a combined exposition to LIF and OSM. In conclusion, we demonstrated that LIF can play a similar role as OSM in the hepatocyte differentiation process of human MSCs.
目前,大多数用于间充质干细胞(MSCs)肝细胞分化的方案都是使用抑瘤素M(OSM)作为肝细胞样成熟的诱导剂。由于白血病抑制因子(LIF)和OSM具有相似的信号通路,我们研究了LIF是否能在肝细胞分化过程中发挥作用。设计了一种使用LIF作为成熟细胞因子的分化方案,并将其与应用于骨髓来源的人MSCs的标准方案和对照方案进行比较。我们观察到,间充质来源的肝细胞样细胞(MDHLCs)在暴露于LIF或OSM时会出现相似的形态变化。通过蛋白质和基因表达分析,我们发现在两种分化条件下肝脏标志物的表达相当。此外,通过尿素分泌和糖原沉积评估证明,LIF和OSM能使MDHLCs获得同等水平的肝细胞样功能。然而,在MDHLCs同时暴露于LIF和OSM后,未观察到肝细胞样特征表达增加。总之,我们证明了LIF在人MSCs的肝细胞分化过程中可以发挥与OSM类似的作用。