Jin Meixian, Yi Xiao, Zhu Xiaojuan, Hu Wei, Wang Simin, Chen Qi, Yang Wanren, Li Yang, Li Shao, Peng Qing, Pan Mingxin, Gao Yi, Xu Shiyuan, Zhang Ying, Zhou Shuqin
Department of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou 510000, China.
Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou 510000, China.
iScience. 2024 Jan 15;27(2):108912. doi: 10.1016/j.isci.2024.108912. eCollection 2024 Feb 16.
Human umbilical cord mesenchymal stem cells (UC-MSCs)-derived hepatocyte-like cells (HLCs) have shown great promise in the treatment of liver diseases. However, most current induction protocols yield hepatocyte-like cells with limited function as compared with primary hepatocytes. Schisandrin B (Sch B) is one of the main components of , which can prevent fibrosis progression and promote liver cell regeneration. Herein, we investigated the effects of Sch B on hepatic differentiation of UC-MSCs. We found that treatment with 10 μM Sch B from the second stage of the differentiation process increased hepatic marker levels and hepatic function. Additionally, RNA-seq analysis revealed that Sch B promoted hepatic differentiation via activating the JAK2/STAT3 pathway. When transplanted HLCs into mice with CCL-induced liver fibrosis, Sch B-treated HLCs exhibited significant therapeutic effects. This study provides an optimized hepatic differentiation protocol for UC-MSCs based on Sch B, yielding functioning cells for liver disease treatment.
人脐带间充质干细胞(UC-MSCs)来源的肝样细胞(HLCs)在肝病治疗中显示出巨大潜力。然而,与原代肝细胞相比,目前大多数诱导方案产生的肝样细胞功能有限。五味子乙素(Sch B)是[此处原文缺失相关信息]的主要成分之一,可阻止纤维化进展并促进肝细胞再生。在此,我们研究了Sch B对UC-MSCs向肝分化的影响。我们发现,从分化过程的第二阶段开始用10 μM Sch B处理可提高肝脏标志物水平和肝功能。此外,RNA测序分析表明,Sch B通过激活JAK2/STAT3途径促进肝分化。当将HLCs移植到CCL诱导的肝纤维化小鼠中时,经Sch B处理的HLCs表现出显著的治疗效果。本研究基于Sch B为UC-MSCs提供了一种优化的肝分化方案,可产生用于肝病治疗的功能性细胞。