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Wandzioch E , Zaret KS
Dynamic signaling network for the specification of embryonic pancreas and liver progenitors
Science. 2009 Jun 26;324(5935) :1707-10
PMID: 19556507    PMCID: PMC 2771431   
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Abstract
Studies of the formation of pancreas and liver progenitors have focused on individual inductive signals and cellular responses. Here, we investigated how bone morphogenetic protein, transforming growth factor-beta (TGFbeta), and fibroblast growth factor signaling pathways converge on the earliest genes that elicit pancreas and liver induction in mouse embryos. The inductive network was found to be dynamic; it changed within hours. Different signals functioned in parallel to induce different early genes, and two permutations of signals induced liver progenitor domains, which revealed flexibility in cell programming. Also, the specification of pancreas and liver progenitors was restricted by the TGFbeta pathway. These findings may enhance progenitor cell specification from stem cells for biomedical purposes and can help explain incomplete programming in stem cell differentiation protocols.
Notes
Wandzioch, Ewa Zaret, Kenneth S R37GM36477/GM/NIGMS NIH HHS/United States U01DK072503/DK/NIDDK NIH HHS/United States Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't United States Science (New York, N.Y.) Science. 2009 Jun 26;324(5935):1707-10.