Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2008
Published online before print April 24, 2008, doi: 10.1161/CIRCRESAHA.108.175505
A more recent version of this article appeared on May 9, 2008
This Article
Right arrow Full Text (PDF)
Right arrow Data Supplement
Right arrow All Versions of this Article:
102/9/1008    most recent
CIRCRESAHA.108.175505v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 van Laake, L. W.
Right arrow Articles by Mummery, C. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by van Laake, L. W.
Right arrow Articles by Mummery, C. L.
Related Collections
Right arrow Animal models of human disease

Submitted on March 12, 2008
Revised on April 1, 2008
Accepted on April 10, 2008

Human Embryonic Stem Cell–Derived Cardiomyocytes and Cardiac Repair in Rodents

Linda W. van Laake ; Robert Passier ; Pieter A. Doevendans ; and Christine L. Mummery *

From the Hubrecht Institute (L.W.v.L., R.P., C.L.M.), Utrecht; Heart Lung Center Utrecht (L.W.v.L., P.A.D.); and Department of Anatomy and Embryology (R.P., C.L.M.), Leiden University Medical Center, The Netherlands.

* To whom correspondence should be addressed. E-mail: c.mummery{at}niob.knaw.nl.

Cell transplantation may restore heart function in disease associated with loss or dysfunction of cardiomyocytes. Recently, Laflamme et al reported an improvement in cardiac function in immunodeficient rats 4 weeks after coronary artery ligation and injection of human embryonic stem cell–derived cardiomyocytes (hESC-CMs). We have recently carried out a comparable study transplanting hESC-CMs to the hearts of mice with myocardial infarction. Our findings were similar up to the 4-week time point, with significant improvements in cardiac function. However, our follow-up was longer, and, at 3 months, the difference between mice receiving cardiomyocytes and those receiving other cells was no longer significant. Hypothesizing that the improvement observed by Laflamme et al may have been more likely to be sustained long term because the grafts in their study appeared larger, we injected 3 times as many cells. Although this resulted in a significantly increased graft size, we again observed a functional improvement at 1 month but not at 3 months. Our results show that midterm data in these kinds of experiments must be interpreted with caution and longer-term follow-up is essential to draw conclusions on the efficacy of cardiac cell transplantation. Furthermore, our findings demonstrate the unlikely success of merely generating and injecting more cells of the same type to increase functional improvement.


Key words: cell transplantation • MRI • myocardial infarction • stem cells




This article has been cited by other articles:


Home page
DMMHome page
K. D. Boudoulas and A. K. Hatzopoulos
Cardiac repair and regeneration: the Rubik's cube of cell therapy for heart disease
Dis. Model. Mech., July 1, 2009; 2(7-8): 344 - 358.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
E. Tanaka and B. Galliot
Triggering the regeneration and tissue repair programs
Development, February 1, 2009; 136(3): 349 - 353.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
K. R. Chien, I. J. Domian, and K. K. Parker
Cardiogenesis and the Complex Biology of Regenerative Cardiovascular Medicine
Science, December 5, 2008; 322(5907): 1494 - 1497.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
J. C. Wu
Molecular Imaging: Antidote to Cardiac Stem Cell Controversy
J. Am. Coll. Cardiol., November 11, 2008; 52(20): 1661 - 1664.
[Full Text] [PDF]


Home page
CirculationHome page
N. L. Tulloch, L. Pabon, and C. E. Murry
Get With the (Re)Program: Cardiovascular Potential of Skin-Derived Induced Pluripotent Stem Cells
Circulation, July 29, 2008; 118(5): 472 - 475.
[Full Text] [PDF]