再生(生物学)
生物
祖细胞
肝再生
肝细胞
肝损伤
祖细胞
细胞生物学
干细胞
肝细胞
平衡
细胞分化
转录组
诱导多能干细胞
硫氧化物9
重编程
谱系(遗传)
胚胎干细胞
肝细胞核因子
遗传学
基因
内科学
内分泌学
转录因子
医学
体外
作者
Xiao Han,Yue Wang,Wenjuan Pu,Xiuzhen Huang,Lin Qiu,Yan Li,Wei Yu,Huan Zhao,Xiuxiu Liu,Lingjuan He,Libo Zhang,Yong Ji,Jie Lü,Kathy O. Lui,Bin Zhou
标识
DOI:10.1016/j.stemcr.2019.01.010
摘要
Elucidation of the role of different cell lineages in the liver could offer avenues to drive liver regeneration. Previous studies showed that SOX9+ hepatocytes can differentiate into ductal cells after liver injuries. It is unclear whether SOX9+ hepatocytes are uni- or bipotent progenitors at a single-cell level during liver injury. Here, we developed a genetic tracing system to delineate the lineage potential of SOX9+ hepatocytes during liver homeostasis and regeneration. Fate-mapping data showed that these SOX9+ hepatocytes respond specifically to different liver injuries, with some contributing to a substantial number of ductal cells. Clonal analysis demonstrated that a single SOX9+ hepatocyte gives rise to both hepatocytes and ductal cells after liver injury. This study provides direct evidence that SOX9+ hepatocytes can serve as bipotent progenitors after liver injury, producing both hepatocytes and ductal cells for liver repair and regeneration.
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