The long-term objective of this research proposal is to fully characterize the role of Proxl in embryonic and adult lymphangiogenesis. Our laboratory has previously shown that Proxl is critical for the development of the lymphatic vasculature and that Proxl heterozygous mice exhibit a mispatterned and dysfunctional lymphatic system. Furthermore, the fact that Proxl is also expressed in adult mouse lymphatic vessels suggested a likely functional role of Proxl in adult stage lymphagiogenesis in instances of wound healing and inflammation. My research project will strive to fully characterize the lymphatic defects seen in Proxl heterozygous mice using both standard knockout and inducible knockout mouse strains. A combination of cellular and molecular approaches will be used to explore the role of Proxl in both embryonic and adult lymphangiogenesis and to identify the different sources of lymphatic endothelial cell precursors. Taken together, these findings will further advance our knowledge of the developing lymphatic system. ? ? ?

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 #
5F32HD051187-02
Application #
7215718
Study Section
Special Emphasis Panel (ZRG1-F05-J (20))
Program Officer
Coulombe, James N
Project Start
2006-05-01
Project End
2009-04-30
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
2
Fiscal Year
2007
Total Cost
$48,796
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Johnson, Nicole C; Dillard, Miriam E; Baluk, Peter et al. (2008) Lymphatic endothelial cell identity is reversible and its maintenance requires Prox1 activity. Genes Dev 22:3282-91