Is it the undifferentiated stem cell, the endothelial progenitor cell, or the mature endothelial cell that has the greatest therapeutic potential for neovascularization? We hypothesize that it is the endothelial progenitor cell, and not the mature endothelial cell, that gives rise to more actively migrating, proliferating cells that are better able to build new vessels and adapt and integrate with the host microenvironment. The goal of the proposed research project is to investigate and compare the developmental stages at which maturing endothelial cells will optimally form new blood vessels and integrate with the host vasculature. Mouse embryonic stem cells (ESC) will be used for these studies because they provide an ideal in vitro system for stem cell differentiation. Cell populations will be isolated at 4 distinct stages of differentiation from an undifferentiated ESC through a mature endothelial cell. The vasculogenic and angiogenic potential of the 4 cell populations will be examined using in vitro collagen gel assays and the whole animal chick chorioallantioc membrane (CAM) assay.
Specific aims are:
Aim 1 - Efficient generation and characterization of the 4 distinct stages of vascular differentiation. These will include: a.) undifferentiated ESC, b.) Flk-1 positive vascular progenitor cells, c.) outgrowths from Flk-1 positive vascular progenitor cells including EC and SMC, and d.) purified and expanded endothelial cells.
Aim 2 - Determine the precise developmental stage at which maturing endothelial cells will optimally generate new vessels in collagen gels.
Aim 3 - Determine the precise developmental stage at which maturing endothelial cells will optimally generate new vessels on the chick CAM. The generation of stem cells at the appropriate stage of development for the growth of new vessels will be important when using these cells for repair of dead heart tissue or damaged or diseased blood vessels.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31HL087716-04
Application #
7821411
Study Section
Special Emphasis Panel (ZRG1-DIG-H (29))
Program Officer
Meadows, Tawanna
Project Start
2007-05-01
Project End
2011-04-30
Budget Start
2010-05-01
Budget End
2011-04-30
Support Year
4
Fiscal Year
2010
Total Cost
$41,380
Indirect Cost
Name
University of California Merced
Department
Type
Schools of Engineering
DUNS #
113645084
City
Merced
State
CA
Country
United States
Zip Code
95343
Blancas, Alicia A; Wong, Lian E; Glaser, Drew E et al. (2013) Specialized tip/stalk-like and phalanx-like endothelial cells from embryonic stem cells. Stem Cells Dev 22:1398-407
Blancas, Alicia A; Shih, Albert J; Lauer, Nicholas E et al. (2011) Endothelial cells from embryonic stem cells in a chemically defined medium. Stem Cells Dev 20:2153-61
Blancas, Alicia A; Chen, Chi-Shuo; Stolberg, Sarah et al. (2011) Adhesive forces in embryonic stem cell cultures. Cell Adh Migr 5:472-9
Blancas, Alicia A; Lauer, Nicholas E; McCloskey, Kara E (2008) Endothelial differentiation of embryonic stem cells. Curr Protoc Stem Cell Biol Chapter 1:Unit 1F.5