类有机物
细胞生物学
肝细胞
肝星状细胞
肝细胞学
正弦波
生物
体外
生物化学
免疫学
内分泌学
肝脏代谢
作者
Knut Rennert,Sandra Steinborn,Marko Gröger,Birgit Ungerböck,Anne‐Marie Jank,Josef Ehgartner,Sándor Nietzsche,J. E. Dinger,Michael Kiehntopf,Harald Funke,Frank T. Peters,Amelie Lupp,Claudia Gärtner,Torsten Mayr,Michael Bauer,Otmar Huber,Alexander S. Mosig
出处
期刊:Biomaterials
[Elsevier BV]
日期:2015-08-25
卷期号:71: 119-131
被引量:235
标识
DOI:10.1016/j.biomaterials.2015.08.043
摘要
Within the liver, non-parenchymal cells (NPCs) are critically involved in the regulation of hepatocyte polarization and maintenance of metabolic function. We here report the establishment of a liver organoid that integrates NPCs in a vascular layer composed of endothelial cells and tissue macrophages and a hepatic layer comprising stellate cells co-cultured with hepatocytes. The three-dimensional liver organoid is embedded in a microfluidically perfused biochip that enables sufficient nutrition supply and resembles morphological aspects of the human liver sinusoid. It utilizes a suspended membrane as a cell substrate mimicking the space of Disse. Luminescence-based sensor spots were integrated into the chip to allow online measurement of cellular oxygen consumption. Application of microfluidic flow induces defined expression of ZO-1, transferrin, ASGPR-1 along with an increased expression of MRP-2 transporter protein within the liver organoids. Moreover, perfusion was accompanied by an increased hepatobiliary secretion of 5(6)-carboxy-2',7'-dichlorofluorescein and an enhanced formation of hepatocyte microvilli. From this we conclude that the perfused liver organoid shares relevant morphological and functional characteristics with the human liver and represents a new in vitro research tool to study human hepatocellular physiology at the cellular level under conditions close to the physiological situation.
科研通智能强力驱动
Strongly Powered by AbleSci AI