Berg Tove, Rountree C Bart, Lee Lily, Estrada Joaquin, Sala Fréderic G, Choe Andrea, Veltmaat Jacqueline M, De Langhe Stijn, Lee Rene, Tsukamoto Hide, Crooks Gay M, Bellusci Saverio, Wang Kasper S
Saban Research Institute, Childrens Hospital Los Angeles, CA 90027, USA.
Hepatology. 2007 Oct;46(4):1187-97. doi: 10.1002/hep.21814.
Fibroblast growth factor (FGF) signaling and beta-catenin activation have been shown to be crucial for early embryonic liver development. This study determined the significance of FGF10-mediated signaling in a murine embryonic liver progenitor cell population as well as its relation to beta-catenin activation. We observed that Fgf10(-/-) and Fgfr2b(-/-) mouse embryonic livers are smaller than wild-type livers; Fgf10(-/-) livers exhibit diminished proliferation of hepatoblasts. A comparison of beta-galactosidase activity as a readout of Fgf10 expression in Fgf10(+/LacZ) mice and of beta-catenin activation in TOPGAL mice, demonstrated peak Fgf10 expression from E9 to E13.5 coinciding with peak beta-catenin activation. Flow cytometric isolation and marker gene expression analysis of LacZ(+) cells from E13.5 Fgf10(+/LacZ) and TOPGAL livers, respectively, revealed that Fgf10 expression and beta-catenin signaling occur distinctly in stellate/myofibroblastic cells and hepatoblasts, respectively. Moreover, hepatoblasts express Fgfr2b, which strongly suggests they can respond to recombinant FGF10 produced by stellate cells. Fgfr2b(-/-)/TOPGAL(+/+) embryonic livers displayed less beta-galactosidase activity than livers of Fgfr2b(+/+)/TOPGAL(+/+) littermates. In addition, cultures of whole liver explants in Matrigel or cell in suspension from E12.5 TOPGAL(+/+)mice displayed a marked increase in beta-galactosidase activity and cell survival upon treatment with recombinant FGF10, indicating that FGFR (most likely FGFR2B) activation is upstream of beta-catenin signaling and promote hepatoblast survival.
Embryonic stellate/myofibroblastic cells promote beta-catenin activation in and survival of hepatoblasts via FGF10-mediated signaling. We suggest a role for stellate/myofibroblastic FGF10 within the liver stem cell niche in supporting the proliferating hepatoblast.
成纤维细胞生长因子(FGF)信号传导和β-连环蛋白激活已被证明对早期胚胎肝脏发育至关重要。本研究确定了FGF10介导的信号传导在小鼠胚胎肝祖细胞群体中的意义及其与β-连环蛋白激活的关系。我们观察到Fgf10(-/-)和Fgfr2b(-/-)小鼠胚胎肝脏比野生型肝脏小;Fgf10(-/-)肝脏中肝母细胞的增殖减少。比较Fgf10(+/LacZ)小鼠中作为Fgf10表达读数的β-半乳糖苷酶活性和TOPGAL小鼠中的β-连环蛋白激活,结果表明从E9到E13.5期间Fgf10表达达到峰值,与β-连环蛋白激活的峰值一致。分别对来自E13.5 Fgf10(+/LacZ)和TOPGAL肝脏的LacZ(+)细胞进行流式细胞术分离和标记基因表达分析,结果显示Fgf10表达和β-连环蛋白信号传导分别在星状/肌成纤维细胞和肝母细胞中明显发生。此外,肝母细胞表达Fgfr2b,这强烈表明它们可以对星状细胞产生的重组FGF10作出反应。Fgfr2b(-/-)/TOPGAL(+/ +)胚胎肝脏显示出比Fgfr2b(+/ +)/TOPGAL(+/ +)同窝仔肝脏更低的β-半乳糖苷酶活性。此外,用重组FGF10处理E12.5 TOPGAL(+/ +)小鼠的全肝外植体培养物或悬浮细胞后,β-半乳糖苷酶活性和细胞存活率显著增加,表明FGFR(最可能是FGFR2B)激活在β-连环蛋白信号传导上游并促进肝母细胞存活。
胚胎星状/肌成纤维细胞通过FGF10介导的信号传导促进肝母细胞中的β-连环蛋白激活和存活。我们认为星状/肌成纤维细胞FGF10在肝干细胞龛中对支持增殖的肝母细胞发挥作用。