Wnt proteins signal through either the canonical Wnt/beta-catenin or the noncanonical Wnt/Ca2+ pathway. In some vertebrates, these pathways have been shown to function antagonistically. The beta-catenin pathway has been implicated in the maintenance and renewal of a variety of stem cells, including human embryonic stem cells (HESCs). The role of the Wnt/Ca2+ pathway in HESCs is unknown. The goal of this research is to determine the role of Wnt/Ca2+ signaling in the self-renewal and differentiation of HESCs. Stem cells (H7 or WA07 and HSF-6 or UC06) will be treated with either canonical or noncanonical purified Wnts or Wnt conditioned media. HESCs will also be transduced with lentivirus that express inducible conditional alleles capable of beta-catenin or Ca2+ directed signaling. Stem cells will be identified by staining for specific markers; also, their ability to differentiate into tissue derived from all three germ layers will be assessed by quantitative RT-PCR of specific tissue markers and by the ability to form teratomas upon injection into NOD/SCID mice. This research will enhance our understanding of the requirements for stem cell propagation, which, in turn, may contribute to the treatment of such diseases as diabetes and hemophilia.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32HD049208-01
Application #
6885243
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Tasca, Richard J
Project Start
2005-01-01
Project End
2005-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
1
Fiscal Year
2005
Total Cost
$57,536
Indirect Cost
Name
University of Washington
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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