The goal of this project is to understand how specification and patterning of internal organs is accomplished during vertebrate embryogenesis, with a particular focus on the origins of the vascular and hematopoietic components of the circulatory system. We have previously characterized a number of zebrafish mutants that cause specific defects in the early development of either blood vessels or blood cells. We have also developed new experimental techniques for studying circulatory development in zebrafish embryos, including embryonic blood cell transfusion and 3-D confocal microangiography. Using these and other genetic and experimental tools we are attempting to (1) elucidate the embryonic origins of vascular endothelial cells and hematopoietic stem cells and determine how these two lineages are related, and (2) understand how the patterning of the developing vasculature is directed. We have already been able to show that single gene defects such as the gridlock mutation can cause defined, localized defects in the patterning of blood vessels. We are now trying to further define the nature and consequences of gridlock and other potential vascular patterning mutations using a variety of genetic, experimental embryologic, molecular, and molecular genetic methods. We are also studying dorsoventral specification and patterning of the major axial trunk vessels (axial artery or aorta and axial vein. We have obtained evidence supporting a """"""""two-signal model"""""""" for axial vessel formation reminiscent of that invoked to explain the dorsoventral patterning of the neural tube, and we are working to understand the nature and activities of these signals. We are also further studying hematopoietic-specific mutations, with emphasis on several early-acting mutations which may cause defects in the formation of hematopoietic progenitor cells.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Intramural Research (Z01)
Project #
1Z01HD001011-01
Application #
6162467
Study Section
Special Emphasis Panel (LMG)
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1997
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Prendergast, Andrew; Linbo, Tor H; Swarts, Tanya et al. (2012) The metalloproteinase inhibitor Reck is essential for zebrafish DRG development. Development 139:1141-52
Isogai, Sumio; Hitomi, Jiro; Yaniv, Karina et al. (2009) Zebrafish as a new animal model to study lymphangiogenesis. Anat Sci Int 84:102-11
Swift, Matthew R; Weinstein, Brant M (2009) Arterial-venous specification during development. Circ Res 104:576-88
Dejana, Elisabetta; Tournier-Lasserve, Elisabeth; Weinstein, Brant M (2009) The control of vascular integrity by endothelial cell junctions: molecular basis and pathological implications. Dev Cell 16:209-21
Gore, Aniket V; Lampugnani, Maria Grazia; Dye, Louis et al. (2008) Combinatorial interaction between CCM pathway genes precipitates hemorrhagic stroke. Dis Model Mech 1:275-81
Anderson, Matthew J; Pham, Van N; Vogel, Andreas M et al. (2008) Loss of unc45a precipitates arteriovenous shunting in the aortic arches. Dev Biol 318:258-67
Alvarez, Yolanda; Cederlund, Maria L; Cottell, David C et al. (2007) Genetic determinants of hyaloid and retinal vasculature in zebrafish. BMC Dev Biol 7:114
Pham, Van N; Lawson, Nathan D; Mugford, Joshua W et al. (2007) Combinatorial function of ETS transcription factors in the developing vasculature. Dev Biol 303:772-83
Cha, Young Ryun; Weinstein, Brant M (2007) Visualization and experimental analysis of blood vessel formation using transgenic zebrafish. Birth Defects Res C Embryo Today 81:286-96
Buchner, David A; Su, Fengyun; Yamaoka, Jennifer S et al. (2007) pak2a mutations cause cerebral hemorrhage in redhead zebrafish. Proc Natl Acad Sci U S A 104:13996-4001

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