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Transplantation of mesenchymal stem cells within a poly(lactide-co-epsilon-caprolactone) scaffold improves cardiac function in a rat myocardial infarction model

Authors
Jin, JiyongJeong, Sung InShin, Young MinLim, Kwang SukShin, Heung SooLee, Young MooKoh, Hyun ChulKim, Kyung-Soo
Issue Date
Feb-2009
Publisher
Elsevier BV
Keywords
Myocardial infarction; Heart failure; Mesenchymal stem cell; Poly(lactide-co-epsilon-caprolactone); Cardiac tissue engineering; Scaffold
Citation
European Journal of Heart Failure, v.11, no.2, pp 147 - 153
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
European Journal of Heart Failure
Volume
11
Number
2
Start Page
147
End Page
153
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/177312
DOI
10.1093/eurjhf/hfn017
ISSN
1388-9842
1879-0844
Abstract
Cardiac tissue engineering has been proposed as an appropriate method to repair myocardial infarction (MI). Evidence suggests that a cell with scaffold combination was more effective than a cell-only implant. Nevertheless, to date, there has been no research into elastic biodegradable poly(lactide-co-epsilon-caprolactone) (PLCL) scaffolds. The aim of this study was to investigate the effect of mesenchymal stem cells (MSCs) with elastic biodegradable PLCL scaffold transplants in a rat MI model. Ten days after inducing MI through the cryoinjury method, a saline control, MSC, PLCL scaffold, or MSC-seeded PLCL scaffold was transplanted onto the hearts. Four weeks after transplantation, cardiac function and histology were evaluated. Transplanted MSCs survived and differentiated into cardiomyocytes in the injured region. Left ventricular ejection fraction in the MSC + PLCL group increased by 23% compared with that in the saline group; it was also higher in the MSC group. The infarct area in the MSC + PLCL group was decreased by 29% compared with that in the saline group; it was also reduced in the MSC group. Mesenchymal stem cells plus PLCL should be an excellent combination for cardiac tissue engineering.
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