The goal of this proposal is to advance technologies and understanding about the mechanism of pancreatic beta cell development in embryogenesis and adult islets, and to promote the application of such advances to islet regeneration and stem cell biology by other members of the Beta Cell Biology Consortium (BCBC). I propose to bring two technologies to the BCBC;one will identify new and unanticipated transcription factor-based regulatory events that are relevant to endocrine development, and the other will define endothelial cell signaling factors that promote endocrine differentiation and pancreatic stromal cell survival. In our first Aim, we will generate in vivo footprinting data and related information on proendocrine transcription factor genes at different stages of pancreatic development and aging, to better define regulatory events that govern endocrine progenitor cell differentiation and beta cell regenerative capacity. By disseminating data to members of the BCBC, collaborators can help us define new factor-regulatory sequence interactions and use the information to monitor, predict, and ultimately perturb beta cell generation from stem cells and during islet regeneration. This approach is complementary to existing genetic studies, which give terminal phenotypes but not information about genetic regulatory mechanisms. In our second Aim, we will use existing endothelial cell lines and create new ones from mouse embryos to identify endothelial signaling factors that promote endocrine progenitor differentiation and pancreatic stromal cell survival. Since endothelial cells and stromal cells both control pancreatic growth, these studies are intended to reveal new signaling molecules that control islet development and regeneration. We also plan to link Aims 1 and 2 by investigating transcription factor occupancies at pro-endocrine genes in response to endothelial signals. By sharing technology and information from our work with the BCBC, our basic developmental studies will be more rapidly translated to develop cures for diabetes

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project--Cooperative Agreements (U01)
Project #
7U01DK072503-05
Application #
7684819
Study Section
Special Emphasis Panel (ZDK1-GRB-3 (M3))
Program Officer
Sato, Sheryl M
Project Start
2005-08-01
Project End
2010-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
5
Fiscal Year
2009
Total Cost
$640,838
Indirect Cost
Name
University of Pennsylvania
Department
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Xu, Cheng-Ran; Li, Lin-Chen; Donahue, Greg et al. (2014) Dynamics of genomic H3K27me3 domains and role of EZH2 during pancreatic endocrine specification. EMBO J 33:2157-70
Serup, Palle; Gustavsen, Carsten; Klein, Tino et al. (2012) Partial promoter substitutions generating transcriptional sentinels of diverse signaling pathways in embryonic stem cells and mice. Dis Model Mech 5:956-66
Metzger, David E; Gasperowicz, Malgorzata; Otto, Florian et al. (2012) The transcriptional co-repressor Grg3/Tle3 promotes pancreatic endocrine progenitor delamination and ?-cell differentiation. Development 139:1447-56
Xu, Cheng-Ran; Zaret, Kenneth S (2012) Chromatin ""pre-pattern"" and epigenetic modulation in the cell fate choice of liver over pancreas in the endoderm. Nucleus 3:150-4
Xu, Cheng-Ran; Cole, Philip A; Meyers, David J et al. (2011) Chromatin ""prepattern"" and histone modifiers in a fate choice for liver and pancreas. Science 332:963-6
Wandzioch, Ewa; Zaret, Kenneth S (2009) Dynamic signaling network for the specification of embryonic pancreas and liver progenitors. Science 324:1707-10
Zaret, K S; Watts, J; Xu, J et al. (2008) Pioneer factors, genetic competence, and inductive signaling: programming liver and pancreas progenitors from the endoderm. Cold Spring Harb Symp Quant Biol 73:119-26
Zaret, Kenneth S; Grompe, Markus (2008) Generation and regeneration of cells of the liver and pancreas. Science 322:1490-4
Freedman, Deborah A; Kashima, Yasushige; Zaret, Kenneth S (2007) Endothelial cell promotion of early liver and pancreas development. Novartis Found Symp 283:207-16;discussion 216-9, 238-41
Wiebe, Peter O; Kormish, Jay D; Roper, Venus T et al. (2007) Ptf1a binds to and activates area III, a highly conserved region of the Pdx1 promoter that mediates early pancreas-wide Pdx1 expression. Mol Cell Biol 27:4093-104