CLC number: Q46; R54
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 0000-00-00
Cited: 25
Clicked: 7745
Chen-yang JIANG, Chun GUI, Ai-na HE, Xin-yang HU, Jie CHEN, Yun JIANG, Jian-an WANG. Optimal time for mesenchymal stem cell transplantation in rats with myocardial infarction[J]. Journal of Zhejiang University Science B, 2008, 9(8): 630-637.
@article{title="Optimal time for mesenchymal stem cell transplantation in rats with myocardial infarction",
author="Chen-yang JIANG, Chun GUI, Ai-na HE, Xin-yang HU, Jie CHEN, Yun JIANG, Jian-an WANG",
journal="Journal of Zhejiang University Science B",
volume="9",
number="8",
pages="630-637",
year="2008",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B0820004"
}
%0 Journal Article
%T Optimal time for mesenchymal stem cell transplantation in rats with myocardial infarction
%A Chen-yang JIANG
%A Chun GUI
%A Ai-na HE
%A Xin-yang HU
%A Jie CHEN
%A Yun JIANG
%A Jian-an WANG
%J Journal of Zhejiang University SCIENCE B
%V 9
%N 8
%P 630-637
%@ 1673-1581
%D 2008
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B0820004
TY - JOUR
T1 - Optimal time for mesenchymal stem cell transplantation in rats with myocardial infarction
A1 - Chen-yang JIANG
A1 - Chun GUI
A1 - Ai-na HE
A1 - Xin-yang HU
A1 - Jie CHEN
A1 - Yun JIANG
A1 - Jian-an WANG
J0 - Journal of Zhejiang University Science B
VL - 9
IS - 8
SP - 630
EP - 637
%@ 1673-1581
Y1 - 2008
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B0820004
Abstract: Background: Bone marrow mesenchymal stem cell (MSC) transplantation is a promising strategy in the treatment of myocardial infarction (MI). However, the time for transplanting cells remains controversial. The aim of this study was to find an optimal time point for cell transplantation. Methods: MSCs were isolated and cultured from Sprague-Dawley (SD) rats. MI model was set up in SD rats by permanent ligation of left anterior descending coronary artery. MSCs were directly injected into the infarct border zone at 1 h, 1 week and 2 weeks after MI, respectively. Sham-operated and MI control groups received equal volume of phosphate buffered saline (PBS). At 4 weeks after MI, cardiac function was assessed by echocardiography; vessel density was analyzed on hematoxylin-eosin stained slides by light microscopy; the apoptosis of cardiomyocytes was evaluated by terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay; the expressions of proteins were analyzed by Western blot. Results: MSC transplantation improved cardiac function, reduced the apoptosis of cardiomyocytes and increased vessel density. These benefits were more obvious in 1-week group than in 1-h and 2-week groups. There are more obvious increases in the ratio of bcl-2/bax and the expression of vascular endothelial growth factor (VEGF) and more obvious decreases in the expression of cleaved-caspase-3 in 1-week group than those in other two groups. Conclusion: MSC transplantation was beneficial for the recovery of cardiac function. MSC transplantation at 1 week post-MI exerted the best effects on increases of cardiac function, anti-apoptosis and angiogenesis.
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