An FGF response pathway that mediates hepatic gene induction in embryonic endoderm cells

被引:118
作者
Calmont, Amelie
Wandzioch, Ewa
Tremblay, Kimberly D.
Minowada, George
Kaestner, Klaus H.
Martin, Gail R.
Zaret, Kenneth S.
机构
[1] Fox Chase Canc Ctr, Program Cell & Dev Biol, Philadelphia, PA 19111 USA
[2] Univ Penn, Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[4] Univ Calif San Francisco, Sch Med, Dept Anat, San Francisco, CA 94158 USA
[5] Univ Calif San Francisco, Sch Med, Program Dev Biol, San Francisco, CA 94158 USA
关键词
D O I
10.1016/j.devcel.2006.06.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While particular combinations of mesodermal signals are known to induce distinct tissue-specific programs in the endoderm, there is little information about the response pathways within endoderm cells that control their specification. We have used signaling inhibitors on embryo tissue explants and whole-embryo cultures as well as genetic approaches to reveal part of an intracellular network by which FGF signaling helps induce hepatic genes and stabilize nascent hepatic cells within the endodermal epithelium. Specifically, we found that hepatic gene induction is elicited by an FGF/MAPK pathway. Although the PI3K pathway is activated in foregut endoderm cells, its inhibition does not block hepatic gene induction in explants; however, it does block tissue growth. We also found that at the onset of hepatogenesis, the FGF/MAPK and PI3K pathways do not crossregulate in the endoderm. The finding of separate pathways for endoderm tissue specification and growth provides insights for guiding cellular regeneration and stem cell differentiation.
引用
收藏
页码:339 / 348
页数:10
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