Liver Cell Biology Research Group, Vrije Universiteit Brussel, Brussels, Belgium.
Methods Mol Biol. 2023;2669:193-206. doi: 10.1007/978-1-0716-3207-9_11.
In vitro models of liver fibrosis have evolved from mono-cultures of primary rodent hepatic stellate cells and stellate cell lines, to more complex co-cultures of primary or stem cell-derived liver cells. Great progress has been made in the development of stem cell-derived liver cultures; however, the liver cells obtained from stem cells do not yet fully recapitulate the phenotype of their in vivo counterparts. Freshly isolated rodent cells remain the most representative cell type to use for in vitro culture. To study liver injury-induced fibrosis, co-cultures of hepatocytes and stellate cells are an informative minimal model. Here, we describe a robust protocol to isolate hepatocytes and hepatic stellate cells from one mouse and a method for the subsequent seeding and culture as free-floating spheroids.
体外肝纤维化模型已经从原代啮齿类肝星状细胞和星状细胞系的单一培养物发展到更复杂的原代或干细胞来源的肝细胞的共培养物。在干细胞衍生的肝培养物的开发方面取得了很大进展;然而,从干细胞获得的肝细胞尚未完全重现其体内对应物的表型。新鲜分离的啮齿动物细胞仍然是用于体外培养的最具代表性的细胞类型。为了研究肝损伤诱导的纤维化,肝细胞和星状细胞的共培养是一种很有信息量的最小模型。在这里,我们描述了一种从一只小鼠中分离肝细胞和肝星状细胞的稳健方案,以及随后作为游离球体播种和培养的方法。