To make a proper blood vessel, several major cellular processes must be regulated and integrated. Specifically, endothelial cell division occurs in the context of morphogenetic processes that lead to sprout formation, fusion, and expansion of the vascular network. Normally these distinct processes are elegantly interwoven to produce the appropriate amount of vasculature with the proper 3-dimensional pattern. However, relatively little is known about how endothelial cell division and morphogenesis are regulated in space and time during angiogenesis, and even less is known about how these processes integrate to form blood vessels. We have evidence that two major aspects of endothelial cell division are regulated by morphogenetic cues, the rate of cell division and the orientation of the cleavage plane during mitosis. Thus we hypothesize that morphogenetic signals impact specific parameters of endothelial cell division, and that this input is critical to proper vessel morphogenesis. We also hypothesize that morphogenetic signals affecting the rate and orientation of endothelial cell division are transduced via endothelial cell-cell junctions and mitotic polarity components. To test these hypotheses, we will use dynamic imaging to elucidate the """"""""rules"""""""" by which endothelial cell division is regulated in time and space during angiogenesis. We will manipulate endothelial junctions and polarity molecules that affect spindle dynamics, and determine the impact of these manipulations on cell division and polarity. Finally, we will examine in detail the role of two signaling pathways, VEGF and Planar Cell Polarity (PCP or non-canonical Wnt signaling) in the co- ordination between endothelial morphogenesis and cell division. A molecular understanding of how cellular processes are integrated during angiogenesis will help in the design of approaches to vessel regeneration. The ability to recapitulate biological processes leading to proper vessel formation is a requirement for many aspects of regenerative medicine, so this work will have high impact in this translational arena. This proposal will use mouse models to examine how the propagation of cells making up the wall of blood vessels affects the form and shape of the vessel. The results will help us understand how vessels are shaped, which in turn will aid in designing ways to make artificial vessels for therapeutic use.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL086564-03
Application #
7655236
Study Section
Special Emphasis Panel (ZRG1-CVS-Q (03))
Program Officer
Goldman, Stephen
Project Start
2007-09-25
Project End
2011-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
3
Fiscal Year
2009
Total Cost
$360,985
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Genetics
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Pelton, John C; Wright, Catherine E; Leitges, Michael et al. (2014) Multiple endothelial cells constitute the tip of developing blood vessels and polarize to promote lumen formation. Development 141:4121-6
Peirce, Shayn M; Mac Gabhann, Feilim; Bautch, Victoria L (2012) Integration of experimental and computational approaches to sprouting angiogenesis. Curr Opin Hematol 19:184-91
Wiley, David M; Kim, Jun-Dae; Hao, Jijun et al. (2011) Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein. Nat Cell Biol 13:686-92
Chappell, John C; Wiley, David M; Bautch, Victoria L (2011) Regulation of blood vessel sprouting. Semin Cell Dev Biol 22:1005-11
Lee, Christina Y; Bautch, Victoria L (2011) Ups and downs of guided vessel sprouting: the role of polarity. Physiology (Bethesda) 26:326-33
Taylor, Sarah M; Nevis, Kathleen R; Park, Hannah L et al. (2010) Angiogenic factor signaling regulates centrosome duplication in endothelial cells of developing blood vessels. Blood 116:3108-17
Chappell, John C; Bautch, Victoria L (2010) Vascular development: genetic mechanisms and links to vascular disease. Curr Top Dev Biol 90:43-72
Chappell, John C; Taylor, Sarah M; Ferrara, Napoleone et al. (2009) Local guidance of emerging vessel sprouts requires soluble Flt-1. Dev Cell 17:377-86
James, Jennifer M; Gewolb, Cara; Bautch, Victoria L (2009) Neurovascular development uses VEGF-A signaling to regulate blood vessel ingression into the neural tube. Development 136:833-41
Bautch, Victoria L; James, Jennifer M (2009) Neurovascular development: The beginning of a beautiful friendship. Cell Adh Migr 3:199-204

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