Current address: Department of Medicine, Division of Cardiology, Emory University, 1639 Pierce Drive-WMB, Atlanta, GA 30322, U.S.A.
Designer blood vessels and therapeutic revascularization
Article first published online: 2 FEB 2009
DOI: 10.1038/sj.bjp.0705457
2003 British Pharmacological Society
Additional Information
How to Cite
Berglund, J. D. and Galis, Z. S. (2003), Designer blood vessels and therapeutic revascularization. British Journal of Pharmacology, 140: 627–636. doi: 10.1038/sj.bjp.0705457
Publication History
- Issue published online: 2 FEB 2009
- Article first published online: 2 FEB 2009
- (Received May 30, 2003, Revised July 8, 2003, Accepted July 16, 2003)
- Abstract
- Article
- References
- Cited By
Keywords:
- Therapeutic revascularization;
- arterial grafts/replacement;
- biodegradable scaffolds;
- angiogenesis;
- arteriogenesis;
- tissue engineering;
- controlled drug delivery;
- nanofabricated devices
Inadequate vascular perfusion leads to fatal heart attacks, chronic ulcers, and other serious clinical conditions. The body's capacity to restore vascular perfusion through angiogenesis and arteriogenesis is often impaired by pre-existing disease, and availability of native replacements for nonfunctional arteries is limited in many patients. Thus, recreating blood vessels of various calibres through novel engineering technologies has emerged as a radical option among therapeutic strategies for revascularization. Ranging from artificial, recycled or reassembled natural conduits to sophisticated microdevices, we refer to these as ‘designer blood vessels’. Our common efforts to continuously improve vascular replacement design have provided many clues about our own blood vessels, but nature's ability to create nonthrombogenic, immunocompatible, strong, yet biologically responsive blood vessels remains unparalleled. Just as art reproductions never equal the original masterpiece, designer blood vessels may never attain nature's perfection. Nevertheless, they will provide a valuable option as long as they come close enough and are available to many.
British Journal of Pharmacology (2003) 140, 627–636. doi:10.1038/sj.bjp.0705457

1476-5381/asset/olbannerleft.gif?v=1&s=198ba9e64c782a75183a18cb494f9d10ecc901ea)
1476-5381/asset/olbannerright.gif?v=1&s=0b2124237bd4227e7991f1ea05cd4bed2496a9ae)
1476-5381/asset/cover.gif?v=1&s=f56f5a76559ff1cebf2b6e329fe028f1e9e0f463)