Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2006;98:1331-1339
Published online before print April 6, 2006, doi: 10.1161/01.RES.0000220650.26555.1d
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
98/10/1331    most recent
01.RES.0000220650.26555.1dv1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wang, H.
Right arrow Articles by Patterson, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, H.
Right arrow Articles by Patterson, C.
Related Collections
Right arrow Angiogenesis
Right arrow Endothelium/vascular type/nitric oxide
(Circulation Research. 2006;98:1331.)
© 2006 American Heart Association, Inc.


Integrative Physiology

Gene Expression Profile Signatures Indicate a Role for Wnt Signaling in Endothelial Commitment From Embryonic Stem Cells

Hong Wang, Peter C. Charles, Yaxu Wu, Rongqin Ren, Xinchun Pi, Martin Moser, Michal Barshishat-Kupper, Jeffrey S. Rubin, Charles Perou, Victoria Bautch, Cam Patterson

From the Carolina Cardiovascular Biology Center (H.W., P.C.C., Y.W., R.R., X.P., M.M., V.B., C. Patterson) and Departments of Medicine (C. Patterson), Biology (V.B.), and Genetics (C. Perou), University of North Carolina, Chapel Hill; and Laboratory of Cellular and Molecular Biology, National Cancer Institute (M.B.-K., J.S.R.), Bethesda, Md.

Correspondence to Cam Patterson, MD, Director, Division of Cardiology and Carolina Cardiovascular Biology Center, 8200 Medical Biomolecular Research Building, Chapel Hill, NC 27599-7126. E-mail cpatters{at}med.unc.edu

We have used global gene expression analysis to establish a comprehensive list of candidate genes in the developing vasculature during embryonic (ES) cell differentiation in vitro. A large set of genes, including growth factors, cell surface molecules, transcriptional factors, and members of several signal transduction pathways that are known to be involved in vasculogenesis or angiogenesis, were found to have expression patterns as expected. Some unknown or functionally uncharacterized genes were differentially regulated in flk1+ cells compared with flk1 cells, suggesting possible roles for these genes in vascular commitment. Particularly, multiple components of the Wnt signaling pathway were differentially regulated in flk1+ cells, including Wnt proteins, their receptors, downstream transcriptional factors, and other components belonging to this pathway. Activation of the Wnt signal was able to expand vascular progenitor populations whereas suppression of Wnt activity reduced flk1+ populations. Suppression of Wnt signaling also inhibited the formation of matured vascular capillary-like structures during late stages of embryoid body differentiation. These data indicate a requisite and ongoing role for Wnt activity during vascular development, and the gene expression profiles identify candidate components of this pathway that participate in vascular cell differentiation.


Key Words: hemangioblast • angiogenesis • microarray • signaling




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
Z. Liu and J. F. Habener
Glucagon-like Peptide-1 Activation of TCF7L2-dependent Wnt Signaling Enhances Pancreatic Beta Cell Proliferation
J. Biol. Chem., March 28, 2008; 283(13): 8723 - 8735.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
P. S. Woll, J. K. Morris, M. S. Painschab, R. K. Marcus, A. D. Kohn, T. L. Biechele, R. T. Moon, and D. S. Kaufman
Wnt signaling promotes hematoendothelial cell development from human embryonic stem cells
Blood, January 1, 2008; 111(1): 122 - 131.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
J. E. Ferguson III, Y. Wu, K. Smith, P. Charles, K. Powers, H. Wang, and C. Patterson
ASB4 Is a Hydroxylation Substrate of FIH and Promotes Vascular Differentiation via an Oxygen-Dependent Mechanism
Mol. Cell. Biol., September 15, 2007; 27(18): 6407 - 6419.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
A. Schmidt, K. Brixius, and W. Bloch
Endothelial Precursor Cell Migration During Vasculogenesis
Circ. Res., July 20, 2007; 101(2): 125 - 136.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
R. Ren, P. C. Charles, C. Zhang, Y. Wu, H. Wang, and C. Patterson
Gene expression profiles identify a role for cyclooxygenase 2-dependent prostanoid generation in BMP6-induced angiogenic responses
Blood, April 1, 2007; 109(7): 2847 - 2853.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
H. Wang, J. B. Gilner, V. L. Bautch, D.-Z. Wang, B. J. Wainwright, S. L. Kirby, and C. Patterson
Wnt2 Coordinates the Commitment of Mesoderm to Hematopoietic, Endothelial, and Cardiac Lineages in Embryoid Bodies
J. Biol. Chem., January 5, 2007; 282(1): 782 - 791.
[Abstract] [Full Text] [PDF]