Ishii Takamichi, Yasuchika Kentaro, Fujii Hideaki, Hoppo Toshitaka, Baba Shinji, Naito Masato, Machimoto Takafumi, Kamo Naoko, Suemori Hirofumi, Nakatsuji Norio, Ikai Iwao
Department of Gastroenterological Surgery, Kyoto University Graduate School of Medicine, 54 Kawahara-cho Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Exp Cell Res. 2005 Sep 10;309(1):68-77. doi: 10.1016/j.yexcr.2005.05.028.
It is difficult to induce the maturation of embryonic stem (ES) cells into hepatocytes in vitro. We previously reported that Thy1-positive mesenchymal cells derived from the mouse fetal liver promote the maturation of hepatic progenitor cells. Here, we isolated alpha-fetoprotein (AFP)-producing cells from mouse ES cells for subsequent differentiation into hepatocytes in vitro by coculture with Thy1-positive cells. ES cells expressing green fluorescent protein (GFP) under the control of an AFP promoter were cultured under serum- and feeder layer-free culture conditions. The proportion of GFP-positive cells plateaued at 41.6 +/- 12.2% (means +/- SD) by day 7. GFP-positive cells, isolated by flow cytometry, were cultured in the presence or absence of Thy1-positive cells as a feeder layer. Isolated GFP-positive cells were stained for AFP, Foxa2, and albumin. The expression of mRNAs encoding tyrosine amino transferase, tryptophan 2,3-dioxygenase, and glucose-6-phosphatase were only detected following coculture with Thy1-positive cells. Following coculture with Thy1-positive cells, the isolated cells produced and stored glycogen. Ammonia clearance activity was also enhanced following coculture. Electron microscopic analysis indicated that the cocultured cells exhibited the morphologic features of mature hepatocytes. In conclusion, coculture with Thy1-positive cells in vitro induced the maturation of AFP-producing cells isolated from ES cell cultures into hepatocytes.
在体外诱导胚胎干细胞(ES细胞)成熟为肝细胞是困难的。我们之前报道过,从小鼠胎肝中分离出的Thy1阳性间充质细胞可促进肝祖细胞的成熟。在此,我们从小鼠ES细胞中分离出产生甲胎蛋白(AFP)的细胞,随后通过与Thy1阳性细胞共培养使其在体外分化为肝细胞。在AFP启动子控制下表达绿色荧光蛋白(GFP)的ES细胞在无血清和无饲养层的培养条件下培养。到第7天时,GFP阳性细胞的比例稳定在41.6±12.2%(平均值±标准差)。通过流式细胞术分离出的GFP阳性细胞在有或无Thy1阳性细胞作为饲养层的情况下进行培养。分离出的GFP阳性细胞进行AFP、Foxa2和白蛋白染色。仅在与Thy1阳性细胞共培养后才检测到编码酪氨酸氨基转移酶、色氨酸2,3-双加氧酶和葡萄糖-6-磷酸酶的mRNA的表达。与Thy1阳性细胞共培养后,分离出的细胞产生并储存糖原。共培养后氨清除活性也增强。电子显微镜分析表明,共培养的细胞呈现出成熟肝细胞的形态特征。总之,体外与Thy1阳性细胞共培养可诱导从ES细胞培养物中分离出的产生AFP的细胞成熟为肝细胞。