Sudo Ryo
Department of System Design Engineering, Keio University, Yokohama, Japan.
Methods Mol Biol. 2019;1905:167-174. doi: 10.1007/978-1-4939-8961-4_15.
Construction of three-dimensional (3D) hepatic tissue structures is important for in vitro tissue engineering of the liver, because 3D culture of hepatocytes is critical for the maintenance of liver-specific functions. Although conventional 3D culture methods are useful for constructing 3D hepatic tissue structures, the precise control of culture microenvironments is required to construct more physiological tissues in vitro. Recent advances in microfluidics technologies have allowed us to utilize microfluidic devices for hepatic cell culture, which opened the door for creating more physiological 3D culture models of the liver. Here, we describe the method for the construction of hepatic tissue structures using a microfluidic device which has a 3D gel region with adjacent microchannels. Primary rat hepatocytes are seeded into a microchannel in a microfluidic device. The cells are then cultured in interstitial flow conditions, which leads to the construction of 3D tissue structures.
构建三维(3D)肝组织结构对于肝脏的体外组织工程至关重要,因为肝细胞的3D培养对于维持肝脏特异性功能至关重要。尽管传统的3D培养方法有助于构建3D肝组织结构,但要在体外构建更具生理功能的组织,需要精确控制培养微环境。微流控技术的最新进展使我们能够利用微流控装置进行肝细胞培养,这为创建更具生理功能的肝脏3D培养模型打开了大门。在此,我们描述了使用具有相邻微通道的3D凝胶区域的微流控装置构建肝组织结构的方法。将原代大鼠肝细胞接种到微流控装置的微通道中。然后在间质流条件下培养细胞,这会导致3D组织结构的构建。