Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2008;103:194-202
Published online before print June 12, 2008, doi: 10.1161/CIRCRESAHA.108.178590
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
103/2/194    most recent
CIRCRESAHA.108.178590v1
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
Google Scholar
Right arrow Articles by Melero-Martin, J. M.
Right arrow Articles by Bischoff, J.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Melero-Martin, J. M.
Right arrow Articles by Bischoff, J.
Related Collections
Right arrow Endothelium/vascular type/nitric oxide
Right arrow Other Vascular biology
Right arrow Angiogenesis
Right arrowRelated Article
(Circulation Research. 2008;103:194.)
© 2008 American Heart Association, Inc.


Integrative Physiology

Engineering Robust and Functional Vascular Networks In Vivo With Human Adult and Cord Blood–Derived Progenitor Cells

Juan M. Melero-Martin, Maria E. De Obaldia, Soo-Young Kang, Zia A. Khan, Lei Yuan, Peter Oettgen, Joyce Bischoff

From the Vascular Biology Program and Department of Surgery, Children’s Hospital Boston (J.M.M.-M., M.E.D.O., S.-Y.K., Z.A.K., J.B.); and Division of Cardiology, Beth Israel Deaconess Medical Center (L.Y., P.O.), Harvard Medical School, Boston Mass.

Correspondence to Dr Joyce Bischoff, Vascular Biology Program and Department of Surgery, Children’s Hospital Boston, Harvard Medical School, Boston, MA 02115. E-mail joyce.bischoff{at}childrens.harvard.edu

The success of therapeutic vascularization and tissue engineering will rely on our ability to create vascular networks using human cells that can be obtained readily, can be expanded safely ex vivo, and can produce robust vasculogenic activity in vivo. Here we describe the formation of functional microvascular beds in immunodeficient mice by coimplantation of human endothelial and mesenchymal progenitor cells isolated from blood and bone marrow. Evaluation of implants after 1 week revealed an extensive network of human blood vessels containing erythrocytes, indicating the rapid formation of functional anastomoses within the host vasculature. The implanted endothelial progenitor cells were restricted to the luminal aspect of the vessels; mesenchymal progenitor cells were adjacent to lumens, confirming their role as perivascular cells. Importantly, the engineered vascular networks remained patent at 4 weeks in vivo. This rapid formation of long-lasting microvascular networks by postnatal progenitor cells obtained from noninvasive sources constitutes an important step forward in the development of clinical strategies for tissue vascularization.


Key Words: vascular networks • endothelial progenitor cells • mesenchymal stem cells • mesenchymal progenitor cells • tissue engineering • regenerative medicine • vasculogenesis • angiogenesis


Related Article:

Therapeutic Vasculogenesis: It Takes Two
Francesco Loffredo and Richard T. Lee
Circ. Res. 2008 103: 128-130. [Full Text] [PDF]



This article has been cited by other articles:


Home page
Circ. Res.Home page
F. Loffredo and R. T. Lee
Therapeutic Vasculogenesis: It Takes Two
Circ. Res., July 18, 2008; 103(2): 128 - 130.
[Full Text] [PDF]