Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Department of Pathology and Immunology, Medical School, University of Geneva, Geneva, Switzerland.
Sci Rep. 2017 Jan 13;7:40322. doi: 10.1038/srep40322.
Cells with slow proliferation kinetics that retain the nuclear label over long time periods-the label-retaining cells (LRCs)-represent multipotent stem cells in a number of adult tissues. Since the identity of liver LRCs (LLRCs) had remained elusive we utilized a genetic approach to reveal LLRCs in normal non-injured livers and characterized their regenerative properties in vivo and in culture. We found that LLRCs were located in biliary vessels and participated in the regeneration of biliary but not hepatocyte injury. In culture experiments the sorted LLRCs displayed an enhanced self-renewal capacity but a unipotent biliary differentiation potential. Transcriptome analysis revealed a unique set of tumorigenesis- and nervous system-related genes upregulated in LLRCs when compared to non-LRC cholangiocytes. We conclude that the LLRCs established during the normal morphogenesis of the liver do not represent a multipotent primitive somatic stem cell population but act as unipotent biliary progenitor cells.
具有缓慢增殖动力学的细胞可以在长时间内保留核标记——标记保留细胞(LRC)——代表了许多成年组织中的多能干细胞。由于肝 LRC(LLRC)的身份一直难以捉摸,我们利用遗传方法在正常未受损的肝脏中揭示了 LLRC,并在体内和体外研究了它们的再生特性。我们发现 LLRC 位于胆管血管中,参与胆管而不是肝细胞损伤的再生。在培养实验中,分选的 LLRC 显示出增强的自我更新能力,但具有单向胆管分化潜能。与非 LRC 胆管细胞相比,转录组分析显示,LLRC 中上调了一组独特的与肿瘤发生和神经系统相关的基因。我们得出结论,在肝脏正常形态发生过程中建立的 LLRC 并不代表多能原始体干细胞群体,而是作为单向胆管祖细胞发挥作用。