School of Life Sciences, Tsinghua University, China.
The Shenzhen Key Laboratory of Health Sciences and Technology, Graduate School at Shenzhen, Tsinghua University, China.
Int J Biol Sci. 2021 Feb 17;17(3):861-868. doi: 10.7150/ijbs.56091. eCollection 2021.
: Compelling evidence suggests that Lgr5+ hepatocytes repair liver damage by promoting the regeneration of hepatocytes and ductal cells in the case of liver injury. The PTEN-mediated AKT/β-catenin signaling plays a key role in the regulation of innate immune regulation in the liver. However, the signaling pathways that control Lgr5+ hepatocyte proliferation in the liver remain unclear. : In order to assess the involvement of PTEN-mediated AKT/β-catenin signaling in the expansion of Lgr5+ hepatocytes upon liver injuries, the Lgr5-CreER; Rosa-mTmG lineage tracing system was used to target Lgr5+ hepatocytes. The tracing of Lgr5+ hepatocytes showed that PTEN deletion and β-catenin activation significantly promoted the proliferation of Lgr5+ hepatocytes. In converse, the simultaneous inhibition of PTEN and β-catenin limited Lgr5+ hepatocyte proliferation in the liver. Our findings provide an insight into understanding how PTEN-mediated AKT/β-catenin signaling regulates the proliferation of Lgr5+ hepatocytes. The outcomes can improve the application potential of Lgr5+ hepatocytes in the treatment of liver injury diseases and provide a new treatment option for liver cancer.
有强有力的证据表明,Lgr5+ 肝细胞通过促进肝损伤时肝细胞和胆管细胞的再生来修复肝损伤。PTEN 介导的 AKT/β-catenin 信号通路在肝脏固有免疫调节中起着关键作用。然而,控制肝脏中 Lgr5+ 肝细胞增殖的信号通路仍不清楚。
为了评估 PTEN 介导的 AKT/β-catenin 信号通路在肝损伤时 Lgr5+ 肝细胞扩增中的作用,使用了 Lgr5-CreER;Rosa-mTmG 谱系追踪系统来靶向 Lgr5+ 肝细胞。Lgr5+ 肝细胞的追踪显示,PTEN 缺失和 β-catenin 激活显著促进了 Lgr5+ 肝细胞的增殖。相反,同时抑制 PTEN 和 β-catenin 限制了 Lgr5+ 肝细胞在肝脏中的增殖。我们的研究结果提供了深入了解 PTEN 介导的 AKT/β-catenin 信号通路如何调节 Lgr5+ 肝细胞增殖的见解。这些结果可以提高 Lgr5+ 肝细胞在治疗肝损伤疾病中的应用潜力,并为肝癌提供新的治疗选择。