Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2000;101:e182-e187

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Reinlib, L.
Right arrow Articles by Field, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Reinlib, L.
Right arrow Articles by Field, L.
Related Collections
Right arrow Other myocardial biology
Right arrow Cell biology/structural biology
Right arrow Gene expression
Right arrow Genetically altered mice
Right arrow Heart failure - basic studies
Right arrow Transplantation
Right arrow Ablation/ICD/surgery
Right arrow CV surgery: other
Right arrow Gene therapy
Right arrow Other Research

(Circulation. 2000;101:e182.)
© 2000 American Heart Association, Inc.


Circulation Electronic Pages

Cell Transplantation as Future Therapy for Cardiovascular Disease?

A Workshop of the National Heart, Lung, and Blood Institute

Leslie Reinlib, PhD; Loren Field, PhD

From the Division of Heart and Vascular Diseases, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Md (L.R.), and the Krannert Institute of Cardiology and Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Ind (L.F.).

Correspondence to Leslie Reinlib, PhD, Division of Heart and Vascular Diseases, National Heart, Lung, and Blood Institute, Rockledge Center Two, 6701 Rockledge Drive, Bethesda, MD 20892-7940. E-mail lr25v{at}nih.gov

Abstract—Despite the development of improved therapies and the significant advances in the understanding of the basis of disease pathogenesis, millions of Americans continue to live with life-threatening cardiovascular diseases. Recent breakthroughs suggest exciting directions that are likely to produce more effective therapies for the treatment of cardiovascular disease. One such area, cell transplantation (grafting of healthy cells into the diseased heart), holds enormous potential as an approach to cardiovascular pathophysiology. Once thought to be a scientific long shot, cell transplantation is becoming recognized as a viable strategy to strengthen weak hearts and limit infarct growth. The technology could also be used for the long-term delivery of beneficial recombinant proteins to the heart, which is a strategy to complement molecular biology advances and provide an alternative strategy for gene therapy. On August 24, 1998, the National Heart, Lung, and Blood Institute convened a workshop to discuss the current status of this fast-moving line of research and to explore its promise for treating cardiovascular disease. The participants included basic and clinical researchers, with representatives from academic and commercial research settings. The workshop was designed to establish the state-of-the-art and to equate current research with practical clinical application. The group recommended short- and long-term goals to assist in realizing, in the most expedient manner, the potential utility of cell transplantation for the treatment of cardiovascular disease. A summary of the meeting discussions and recommendations for future areas of research is presented.


Key Words: cardiovascular diseases • cells • grafting • myocytes




This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Rubart, E. Wang, K. W. Dunn, and L. J. Field
Two-photon molecular excitation imaging of Ca2+ transients in Langendorff-perfused mouse hearts
Am J Physiol Cell Physiol, June 1, 2003; 284(6): C1654 - C1668.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
S. Miyagawa, Y. Sawa, S. Taketani, N. Kawaguchi, T. Nakamura, N. Matsuura, and H. Matsuda
Myocardial Regeneration Therapy for Heart Failure: Hepatocyte Growth Factor Enhances the Effect of Cellular Cardiomyoplasty
Circulation, May 28, 2002; 105(21): 2556 - 2561.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
M. D. Grounds, J. D. White, N. Rosenthal, and M. A. Bogoyevitch
The Role of Stem Cells in Skeletal and Cardiac Muscle Repair
J. Histochem. Cytochem., May 1, 2002; 50(5): 589 - 610.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
T. Shimizu, M. Yamato, Y. Isoi, T. Akutsu, T. Setomaru, K. Abe, A. Kikuchi, M. Umezu, and T. Okano
Fabrication of Pulsatile Cardiac Tissue Grafts Using a Novel 3-Dimensional Cell Sheet Manipulation Technique and Temperature-Responsive Cell Culture Surfaces
Circ. Res., February 22, 2002; 90 (3): e40 - e48.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
K. B. S. Pasumarthi, S.-C. Tsai, and L. J. Field
Coexpression of Mutant p53 and p193 Renders Embryonic Stem Cell-Derived Cardiomyocytes Responsive to the Growth-Promoting Activities of Adenoviral E1A
Circ. Res., May 25, 2001; 88(10): 1004 - 1011.
[Abstract] [Full Text] [PDF]