Vasculogenesis is the de novo formation of blood vessels from mesoderm. Basic steps in the process of vasculogenesis are the generation of angioblasts from undifferentiated mesoderm and the coalescence and transformation of angioblasts into endothelial cells (ECs). In addition, our studies have revealed a subsequent step in the process that involves the fusion of small vessels to form large vessels and vascular sinuses. This process, termed vascular fusion, was discovered as a result of experimentation in which elevated levels of VEGF were shown to lead to uncontrolled fusion, hyperfusion. VEGF-induced hyperfusion has not only been described in embryos of multiple species, but importantly in adult neovascular processes. Indeed, uncontrolled fusion activity now stands as an impediment to the numerous therapeutic uses envisioned for VEGF. Understanding the mechanism(s) by which vascular fusion is controlled has been a focus of our research. As a result we have found that VEGF/VEGF receptor is critical to fusion and hyperfusion and that a correlative relationship exists between the density of ECs and specific vascular patterns. Based on these and other findings we have derived the hypothesis that regulation of EC numbers/density is fundamental to normal vascular fusion and the pathological process of hyperfusion. Major ways to influence EC numbers/density include control of mitosis, apoptosis and/or recruitment of EC progenitor cells from mesoderm. Experimentation outlined in this application will determine the morphological consequences of and the mechanisms by which VEGF-A (VEGF165/VEGFt21) and PLGF signaling via the VEGF receptors (Flkl, Fltl and Neuropilin 1 & 2) impact vascular morphogenesis and act to regulate EC numbers/density. With respect to recruitment of progenitor cells to sites of vasculogenesis, we will also extend on our preliminary findings indicating that circulating embryonic stem cells contribute to vasculogenesis and vascular fusion. A major strength of the proposed research plan is the use of both our well-established in vivo avian assay and a powerful new in vitro murine model of vasculogenesis that recapitulates salient aspects of in vivo vasculogenesis. The proposed research is expected to contribute to a greater understanding of vasculogenesis, vascular fusion, and hyperfusion and offer new perspectives for strategies that target the neovascular component of various diseases.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL057375-09
Application #
7028368
Study Section
Pathology A Study Section (PTHA)
Program Officer
Schramm, Charlene A
Project Start
1997-01-01
Project End
2008-03-31
Budget Start
2006-04-01
Budget End
2008-03-31
Support Year
9
Fiscal Year
2006
Total Cost
$213,854
Indirect Cost
Name
Medical University of South Carolina
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
183710748
City
Charleston
State
SC
Country
United States
Zip Code
29425
Fleming, Paul A; Argraves, W Scott; Gentile, Carmine et al. (2010) Fusion of uniluminal vascular spheroids: a model for assembly of blood vessels. Dev Dyn 239:398-406
Gentile, Carmine; Fleming, Paul A; Mironov, Vladimir et al. (2008) VEGF-mediated fusion in the generation of uniluminal vascular spheroids. Dev Dyn 237:2918-25
Drake, Christopher J; Fleming, Paul A; Argraves, W Scott (2007) The genetics of vasculogenesis. Novartis Found Symp 283:61-71;discussion 71-6, 238-41
LaRue, Amanda C; Masuya, Masahiro; Ebihara, Yasuhiro et al. (2006) Hematopoietic origins of fibroblasts: I. In vivo studies of fibroblasts associated with solid tumors. Exp Hematol 34:208-18
Ebihara, Yasuhiro; Masuya, Masahiro; Larue, Amanda C et al. (2006) Hematopoietic origins of fibroblasts: II. In vitro studies of fibroblasts, CFU-F, and fibrocytes. Exp Hematol 34:219-29
Drake, Christopher J; Wessels, Andy; Trusk, Tom et al. (2006) Elevated vascular endothelial cell growth factor affects mesocardial morphogenesis and inhibits normal heart bending. Dev Dyn 235:10-8
Visconti, Richard P; Ebihara, Yasuhiro; LaRue, Amanda C et al. (2006) An in vivo analysis of hematopoietic stem cell potential: hematopoietic origin of cardiac valve interstitial cells. Circ Res 98:690-6
Argraves, W Scott; Drake, Christopher J (2005) Genes critical to vasculogenesis as defined by systematic analysis of vascular defects in knockout mice. Anat Rec A Discov Mol Cell Evol Biol 286:875-84
Abe, Takanori; Fleming, Paul A; Masuya, Masahiro et al. (2005) Granulocyte/macrophage origin of glomerular mesangial cells. Int J Hematol 82:115-8
Ishikawa, Fumihiko; Drake, Christopher J; Yang, Su et al. (2003) Transplanted human cord blood cells give rise to hepatocytes in engrafted mice. Ann N Y Acad Sci 996:174-85

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