Kim Kyungsook, Utoh Rie, Ohashi Kazuo, Kikuchi Tetsutaro, Okano Teruo
Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.
Department of Molecular Science and Technology, Ajou University, Suwon, 443-749, Korea.
J Tissue Eng Regen Med. 2017 Jul;11(7):2071-2080. doi: 10.1002/term.2102. Epub 2015 Nov 9.
Cell sheet stratification technology has been used for reconstituting highly functional three-dimensional (3D) hepatic tissues in vitro. Triple-layered hepatic tissues with a hepatocyte-specific polarity were fabricated by sandwiching a hepatocyte sheet (Hep sheet) between two endothelial cell (EC) sheets. The morphological and functional characteristics of the triple-layered hepatic construct (EC-Hep-EC) were evaluated and compared with those of a double-layered hepatic construct with a single EC sheet (Hep-EC) and a Hep sheet only. Transmission electron microscope (TEM) observations revealed that the extracellular matrix was observed to be deposited in the space between the ECs and hepatocytes on both the upper and lower sides of the hepatocytes in the EC-Hep-EC construct. Immunohistochemistry with basolateral (CD147) and apical [multidrug resistance-associated protein (MRP2)] membrane polarity markers clearly showed the recovery of in vivo-like hepatocyte polarization in the EC-Hep-EC group. In addition, hepatocyte-specific functions, including albumin secretion, ammonia removal and the induction of cytochrome P450, were also highly preserved. The presented technology for stratifying multiple cell sheets was simple in operation and successfully reproduced both the heterotypic/homotypic cell-cell and cell-matrix interactions with the inherent hepatocyte configurations, thus closely mimicking the in vivo environment. The triple-layered 3D hepatic constructs could therefore be valuable as a new experiment tool for drug-screening tests, an implantable tissue model for cell-based therapies and an efficient culture platform for bioartificial liver devices. Copyright © 2015 John Wiley & Sons, Ltd.
细胞片层分层技术已被用于在体外重建具有高度功能的三维(3D)肝组织。通过将肝细胞片(Hep片)夹在两个内皮细胞(EC)片之间,制备了具有肝细胞特异性极性的三层肝组织。对三层肝构建体(EC-Hep-EC)的形态和功能特性进行了评估,并与具有单个EC片的双层肝构建体(Hep-EC)和仅Hep片进行了比较。透射电子显微镜(TEM)观察显示,在EC-Hep-EC构建体中,肝细胞上下两侧的EC与肝细胞之间的空间中观察到细胞外基质沉积。使用基底外侧(CD147)和顶端[多药耐药相关蛋白(MRP2)]膜极性标记物的免疫组织化学清楚地显示了EC-Hep-EC组中体内样肝细胞极化的恢复。此外,肝细胞特异性功能,包括白蛋白分泌、氨清除和细胞色素P450的诱导,也得到了高度保留。所提出的多层细胞片分层技术操作简单,成功再现了具有固有肝细胞构型的异型/同型细胞-细胞和细胞-基质相互作用,从而紧密模拟了体内环境。因此,三层3D肝构建体作为药物筛选试验的新实验工具、基于细胞疗法的可植入组织模型以及生物人工肝装置的高效培养平台可能具有重要价值。版权所有© 2015 John Wiley & Sons, Ltd.