van Zijl Franziska, Mikulits Wolfgang
Franziska van Zijl, Wolfgang Mikulits, Department of Medicine I, Institute of Cancer Research, Medical University of Vienna, Borschkegasse 8a, A-1090 Vienna, Austria.
World J Hepatol. 2010 Jan 27;2(1):1-7. doi: 10.4254/wjh.v2.i1.1.
Studying physiological and pathophysiological mechanisms in the liver on a molecular basis is a challenging task. During two dimensional (2D) culture conditions hepatocytes dedifferentiate rapidly by losing metabolic functions and structural integrity. Hence, inappropriate 2D hepatocellular models hamper studies on the xenobiotic metabolism of the liver which strongly influences drug potency. Also, the lack of effective therapies against hepatocellular carcinoma shows the urgent need for robust models to investigate liver functions in a defined hepatic microenvironment. Here, we summarize and discuss three-dimensional cultures of hepatocytes, herein referred to as hepatospheres, which provide versatile tools to investigate hepatic metabolism, stemness and cancer development.
在分子层面研究肝脏的生理和病理生理机制是一项具有挑战性的任务。在二维(2D)培养条件下,肝细胞会迅速去分化,失去代谢功能和结构完整性。因此,不合适的二维肝细胞模型会阻碍对肝脏异生物质代谢的研究,而异生物质代谢会强烈影响药物效力。此外,缺乏针对肝细胞癌的有效治疗方法,这表明迫切需要强大的模型来在明确的肝脏微环境中研究肝脏功能。在此,我们总结并讨论肝细胞的三维培养,即本文所指的肝球,它为研究肝脏代谢、干性和癌症发展提供了多功能工具。