Ohno Maki, Motojima Kiyoto, Okano Teruo, Taniguchi Akiyoshi
Advanced Medical Materials Group, Biomaterials Center, National Institute for Materials Science, Tsukuba, Ibaraki, Japan.
J Biochem. 2009 May;145(5):591-7. doi: 10.1093/jb/mvp019. Epub 2009 Jan 27.
We previously reported that using thermo-responsive culture surfaces, a layered co-culture was achieved by placing an endothelial cell sheet onto a layer of human hepatoma cell line HepG2 in order to develop a culture model that mimics hepatic lobules. In the layered co-culture cells, the expression levels of liver-specific genes gradually increased. A cross-sectional view of the layered co-culture cells showed that the thickness of the layer slowly increased after layering, as did extracellular matrix (ECM) deposition around HepG2 cells. In this study, we report that the molecular compositions of ECM and cell-adhesion molecules changed in the layered co-culture cells. Gene expression of integrin alpha4 and decorin gradually increased after layering, and the time-course pattern of these genes was correlated with that of liver-specific genes. Moreover, the layered co-culture system has the ability to assemble a branching network of fibronectin fibrils. These results suggest that a vastly different extracellular environment in layered co-culture cells may induce an increase in liver-specific functions.
我们之前报道过,通过使用热响应性培养表面,将内皮细胞片放置在人肝癌细胞系HepG2层上,实现了分层共培养,以建立一种模拟肝小叶的培养模型。在分层共培养细胞中,肝脏特异性基因的表达水平逐渐升高。分层共培养细胞的横截面视图显示,分层后该层的厚度缓慢增加,HepG2细胞周围的细胞外基质(ECM)沉积情况也是如此。在本研究中,我们报道了分层共培养细胞中ECM和细胞粘附分子的分子组成发生了变化。分层后整合素α4和核心蛋白聚糖的基因表达逐渐增加,这些基因的时间进程模式与肝脏特异性基因的模式相关。此外,分层共培养系统具有组装纤连蛋白原纤维分支网络的能力。这些结果表明,分层共培养细胞中截然不同的细胞外环境可能会诱导肝脏特异性功能的增加。