Skip Navigation

Cardiovascular Research 2006 70(3):530-542; doi:10.1016/j.cardiores.2006.02.016
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Lim, S. Y.
Right arrow Articles by Park, J. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lim, S. Y.
Right arrow Articles by Park, J. C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Copyright © 2006, European Society of Cardiology

The effects of mesenchymal stem cells transduced with Akt in a porcine myocardial infarction model

Sang Yup Lima,1, Yong Sook Kima,1, Youngkeun Ahna,*, Myung Ho Jeonga, Moon Hwa Honga, Soo Yeon Jooa, Kwang Il Namb, Jeong Gwan Choa, Peter M. Kangc and Jong Chun Parka

aDepartment of Cardiovascular Medicine, The Heart Center of Chonnam National University Hospital, 8 Hak Dong, Dong Ku, Gwangju 501-757, South Korea
bResearch Institute of Medical Sciences, Chonnam National University Medical School, Gwangju, South Korea
cCardiovascular Division, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, USA

* Corresponding author. Tel.: +82 62 220 4764; fax: +82 62 223 3105. Email address: cecilyk{at}hanmail.net

Objective This study was designed to examine whether mesenchymal stem cells (MSCs) transduced with Akt enhance cardiac repair after transplantation into the ischemic porcine heart.

Methods MSCs isolated from porcine bone marrow and transduced with myr-Akt were transplanted into porcine hearts after experimental myocardial infarction (MI) using intracoronary injection [Group I, vehicle; Group II, MSCs; Group III, Akt-MSCs]. Myocardial single photon emission tomography (M-SPECT) was performed to assess myocardial function and the infarcted area. Pigs were also sacrificed for immunohistochemical characterization and histologic analysis. In addition, in vitro assays were performed to examine the resistance of Akt-MSCs to H2O2 stimulation.

Results Transplantation of MSCs into the ischemic porcine myocardium (Group II) increased the left ventricular ejection fraction ({delta}LV EF; – 6.3±15.1% versus 0.5±6.4%, P<0.001) and decreased the {delta}area of MI (6.8±5.6% versus – 5.0±5.3%, P<0.001) compared with the vehicle control (Group I). Transplantation of MSCs transduced with myr-Akt (Group III) resulted in further improvement in {delta}LV EF (– 6.3±15.1% versus 5.8±11.3%, P<0.001) and in {delta}area of MI (6.8±5.6% versus – 17.0±7.6%, P<0.001). Akt-MSCs were more resistant to apoptosis, and the levels of extracellular signal-regulated protein kinase (ERK) activation and vascular endothelial growth factor (VEGF) were higher in H2O2-stimulated Akt-MSCs.

Conclusion Cellular transplantation of Akt-MSCs further enhances the repair of injured myocardium compared to MSC transplantation alone by increasing the number of viable MSCs after cellular transplantation.

KEYWORDS Mesenchymal stem cell; Akt; Myocardial infarction; Porcine


1 These authors contributed equally to this work.

Time for primary review 29 days


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Am. J. Physiol. Renal Physiol.Home page
T. Kucic, I. B. Copland, J. Cuerquis, D. L. Coutu, L. E. Chalifour, R. F. Gagnon, and J. Galipeau
Mesenchymal stromal cells genetically engineered to overexpress IGF-I enhance cell-based gene therapy of renal failure-induced anemia
Am J Physiol Renal Physiol, August 1, 2008; 295(2): F488 - F496.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.