Biliary epithelial cells are facultative liver stem cells during liver regeneration in adult zebrafish

被引:12
作者
Oderberg, Isaac M. [1 ]
Goessling, Wolfram [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Div Genet, Boston, MA USA
[2] Harvard Stem Cell Inst, Cambridge, MA USA
[3] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA USA
[4] Broad Inst MIT & Harvard, Cambridge, MA USA
[5] Harvard MIT, Div Hlth Sci & Technol, Boston, MA USA
[6] Harvard Med Sch, Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA USA
关键词
L-FABP GENE; GROWTH-FACTOR; IN-VIVO; HB-EGF; EXPRESSION; DRIVEN; INJURY; HEPATOCYTES; DISEASE; HEART;
D O I
10.1172/jci.insight.163929
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The liver is a highly regenerative organ, yet the presence of a dedicated stem cell population remains controversial. Here, we interrogate a severe hepatocyte injury model in adult zebrafish to define that regeneration involves a stem cell population. After near-total hepatocyte ablation, single-cell transcriptomic and high-resolution imaging analyses throughout the entire regenerative timeline reveal that biliary epithelial cells undergo transcriptional and morphological changes to become hepatocytes. As a population, biliary epithelial cells give rise to both hepatocytes and biliary epithelial cells. Biliary epithelial cells proliferate and dedifferentiate to express hepatoblast transcription factors prior to hepatocyte differentiation. This process is characterized by increased MAPK, PI3K, and mTOR signaling, and chemical inhibition of these pathways impairs biliary epithelial cell proliferation and fate conversion. We conclude that, upon severe hepatocyte ablation in the adult liver, biliary epithelial cells act as facultative liver stem cells in an EGFR-PI3K-mTOR-dependent manner.
引用
收藏
页数:23
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