Howard Hughes Medical Institute, Department of Developmental Biology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Howard Hughes Medical Institute, Department of Developmental Biology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cell. 2018 Nov 29;175(6):1607-1619.e15. doi: 10.1016/j.cell.2018.11.012.
In the healthy adult liver, most hepatocytes proliferate minimally. However, upon physical or chemical injury to the liver, hepatocytes proliferate extensively in vivo under the direction of multiple extracellular cues, including Wnt and pro-inflammatory signals. Currently, liver organoids can be generated readily in vitro from bile-duct epithelial cells, but not hepatocytes. Here, we show that TNFα, an injury-induced inflammatory cytokine, promotes the expansion of hepatocytes in 3D culture and enables serial passaging and long-term culture for more than 6 months. Single-cell RNA sequencing reveals broad expression of hepatocyte markers. Strikingly, in vitro-expanded hepatocytes engrafted, and significantly repopulated, the injured livers of Fah mice. We anticipate that tissue repair signals can be harnessed to promote the expansion of otherwise hard-to-culture cell-types, with broad implications.
在健康成年人的肝脏中,大多数肝细胞增殖很少。然而,在肝脏受到物理或化学损伤后,肝细胞在多种细胞外信号的指导下,包括 Wnt 和促炎信号,在体内广泛增殖。目前,胆管上皮细胞很容易在体外生成肝类器官,但不能生成肝细胞。在这里,我们发现 TNFα(一种损伤诱导的炎症细胞因子)可促进 3D 培养中的肝细胞扩增,并使其能够进行连续传代和长达 6 个月以上的长期培养。单细胞 RNA 测序揭示了广泛的肝细胞标志物表达。引人注目的是,体外扩增的肝细胞可植入并显著重 populate Fah 小鼠受损的肝脏。我们预计,可以利用组织修复信号来促进其他难以培养的细胞类型的扩增,这具有广泛的意义。