Although functional coronary arterial circulation is vital to cardiac viability and function, very little is known about how the branching pathways of the coronary arterial network are established during embryogenesis Our retroviral cell lineage studies of the chick embryos have demonstrated conclusively that coronary progenitors arises from the epicardial anlagen and that coronary progenitors enter the tubular stage heart with the growing epicardial mantle. In addition, coronary vessels are established by vasculogenic mechanisms and not by angiogenic sprouting form the aorta. We have also shown that coronary vasculogenesis is more prominent in the outer than the inner myocardium and serves as a template for coronary arterial development. This morphogenetic process can be altered by the local expression of exogenous genes (e.g., FGF) using retroviral-mediated gene transfer. Finally, ablation of cardiac neural crests results in the loss of differentiation of the intramural, but not the subepicardial, arterial network. These data lead to the central hypothesis that paracrine signals form the myocardium regulate both the directed migration of coronary vessel precursors to the heart (Hypothesis-1) and capillary plexus formation within the heart (Hypothesis-2). We also hypothesis that a sub-population of neural crest-derived cells regulate the differentiation and patterning of the coronary arterial network (Hypothesis-3). We will test these three specific hypotheses by: 1) determining the region-specific interaction between pro-epicardial cells and myocardium-derived instructive signals and analyzing myocardial signaling properties; 2) reprogramming the gradient of the myocyte-derived FGF within the heart wall by using retroviral vectors expressing FGF-ligands and quantifying alteration of coronary patterning using lineage-specific markers; and 3) retrovirally expressing endothelin, NT3/trkC, or their dominant negative mutants to alter their expression in the developing heart and assaying neural crest migration, differentiation and apoptosis in vivo to determine their requirement for intramural arterial development. The studies proposed here will identify the regulators in establishing coronary artery network and build a foundation for rational therapeutics of coronary disorders in adults.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL067105-05
Application #
7053318
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
5
Fiscal Year
2005
Total Cost
$389,279
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Criswell, Tracy L; Dumont, Nancy; Barnett, Joey V et al. (2008) Knockdown of the transforming growth factor-beta type III receptor impairs motility and invasion of metastatic cancer cells. Cancer Res 68:7304-12
Hayashi, Hisaki; Kume, Tsutomu (2008) Foxc transcription factors directly regulate Dll4 and Hey2 expression by interacting with the VEGF-Notch signaling pathways in endothelial cells. PLoS One 3:e2401
Hayashi, Hisaki; Sano, Hideto; Seo, Seungwoon et al. (2008) The Foxc2 transcription factor regulates angiogenesis via induction of integrin beta3 expression. J Biol Chem 283:23791-800
Hayashi, Hisaki; Kume, Tsutomu (2008) Forkhead transcription factors regulate expression of the chemokine receptor CXCR4 in endothelial cells and CXCL12-induced cell migration. Biochem Biophys Res Commun 367:584-9
Austin, Anita F; Compton, Leigh A; Love, Joseph D et al. (2008) Primary and immortalized mouse epicardial cells undergo differentiation in response to TGFbeta. Dev Dyn 237:366-76
Compton, Leigh A; Potash, Dru A; Brown, Christopher B et al. (2007) Coronary vessel development is dependent on the type III transforming growth factor beta receptor. Circ Res 101:784-91
Fujita, Hideo; Kang, Myengmo; Eren, Mesut et al. (2006) Foxc2 is a common mediator of insulin and transforming growth factor beta signaling to regulate plasminogen activator inhibitor type I gene expression. Circ Res 98:626-34
Smith, Travis K; Bader, David M (2006) Characterization of Bves expression during mouse development using newly generated immunoreagents. Dev Dyn 235:1701-8
Compton, Leigh A; Potash, Dru A; Mundell, Nathan A et al. (2006) Transforming growth factor-beta induces loss of epithelial character and smooth muscle cell differentiation in epicardial cells. Dev Dyn 235:82-93
Seo, Seungwoon; Fujita, Hideo; Nakano, Atsushi et al. (2006) The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development. Dev Biol 294:458-70

Showing the most recent 10 out of 23 publications