Ramachandran Sarada Devi, Schirmer Katharina, Münst Bernhard, Heinz Stefan, Ghafoory Shahrouz, Wölfl Stefan, Simon-Keller Katja, Marx Alexander, Øie Cristina Ionica, Ebert Matthias P, Walles Heike, Braspenning Joris, Breitkopf-Heinlein Katja
Medicyte GmbH, Im Neuenheimer Feld 581, 69120, Heidelberg, Germany.
Department of Medicine II, Faculty of Medicine at Mannheim, Heidelberg University, Mannheim, Germany.
PLoS One. 2015 Oct 21;10(10):e0139345. doi: 10.1371/journal.pone.0139345. eCollection 2015.
In this study we used differentiated adult human upcyte® cells for the in vitro generation of liver organoids. Upcyte® cells are genetically engineered cell strains derived from primary human cells by lenti-viral transduction of genes or gene combinations inducing transient proliferation capacity (upcyte® process). Proliferating upcyte® cells undergo a finite number of cell divisions, i.e., 20 to 40 population doublings, but upon withdrawal of proliferation stimulating factors, they regain most of the cell specific characteristics of primary cells. When a defined mixture of differentiated human upcyte® cells (hepatocytes, liver sinusoidal endothelial cells (LSECs) and mesenchymal stem cells (MSCs)) was cultured in vitro on a thick layer of Matrigel™, they self-organized to form liver organoid-like structures within 24 hours. When further cultured for 10 days in a bioreactor, these liver organoids show typical functional characteristics of liver parenchyma including activity of cytochromes P450, CYP3A4, CYP2B6 and CYP2C9 as well as mRNA expression of several marker genes and other enzymes. In summary, we hereby describe that 3D functional hepatic structures composed of primary human cell strains can be generated in vitro. They can be cultured for a prolonged period of time and are potentially useful ex vivo models to study liver functions.
在本研究中,我们使用分化的成人人类upcyte®细胞进行肝类器官的体外生成。Upcyte®细胞是通过慢病毒转导诱导瞬时增殖能力的基因或基因组合(upcyte®过程)从原代人类细胞衍生而来的基因工程细胞系。增殖的upcyte®细胞经历有限次数的细胞分裂,即20至40次群体倍增,但在撤除增殖刺激因子后,它们恢复了原代细胞的大部分细胞特异性特征。当将分化的人类upcyte®细胞(肝细胞、肝窦内皮细胞(LSEC)和间充质干细胞(MSC))的特定混合物在Matrigel™厚层上进行体外培养时,它们在24小时内自组织形成肝类器官样结构。当在生物反应器中进一步培养10天时,这些肝类器官显示出肝实质的典型功能特征,包括细胞色素P450、CYP3A4、CYP2B6和CYP2C9的活性以及几种标记基因和其他酶的mRNA表达。总之,我们在此描述了由原代人类细胞系组成的三维功能性肝结构可以在体外生成。它们可以长时间培养,并且是研究肝功能的潜在有用的体外模型。