Abstract

Since both myocardium and vasculature in the heart are excessively damaged following myocardial infarction (MI), therapeutic strategies for treating MI hearts should concurrently target both so as to achieve true cardiac repair. Here we demonstrate a concomitant method that exploits the advantages of cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) and human mesenchymal stem cell-loaded patch (hMSC-PA) to amplify cardiac repair in a rat MI model. Epicardially implanted hMSC-PA provide a complimentary microenvironment which enhances vascular regeneration through prolonged secretion of paracrine factors, but more importantly it significantly improves the retention and engraftment of intramyocardially injected hiPSC-CMs which ultimately restore the cardiac function. Notably, the majority of injected hiPSC-CMs display adult CMs like morphology suggesting that the secretomic milieu of hMSC-PA constitutes pleiotropic effects in vivo. We provide compelling evidence that this dual approach can be a promising means to enhance cardiac repair on MI hearts.

Details

Title
Dual stem cell therapy synergistically improves cardiac function and vascular regeneration following myocardial infarction
Author
Soon-Jung, Park 1   VIAFID ORCID Logo  ; Ri Youn Kim 2 ; Bong-Woo Park 3   VIAFID ORCID Logo  ; Lee, Sunghun 2   VIAFID ORCID Logo  ; Seong Woo Choi 1 ; Park, Jae-Hyun 4 ; Jong Jin Choi 1 ; Seok-Won, Kim 5 ; Jang, Jinah 6 ; Dong-Woo, Cho 5 ; Hyung-Min, Chung 1 ; Sung-Hwan Moon 7 ; Ban, Kiwon 2   VIAFID ORCID Logo  ; Hun-Jun Park 8 

 Department of Medicine, Konkuk University School of Medicine, Seoul, Republic of Korea 
 Department of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong SAR 
 Department of Medical Life Science, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea; Division of Cardiology, Department of Internal Medicine, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea 
 Division of Cardiology, Department of Internal Medicine, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea 
 Department of Mechanical Engineering, Pohang University of Science and Technology, Nam-gu, Pohang, Republic of Korea 
 Department of Creative IT Engineering and School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Nam-gu, Pohang, Republic of Korea 
 Department of Medicine, Konkuk University School of Medicine, Seoul, Republic of Korea; Research Institute, T&R Biofab Co. Ltd, 237, Siheung, Republic of Korea 
 Department of Medical Life Science, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea; Division of Cardiology, Department of Internal Medicine, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea; Cell Death Disease Research Center, College of Medicine, The Catholic University of Korea, Seocho-gu, Seoul, Republic of Korea 
Pages
1-12
Publication year
2019
Publication date
Jul 2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2258701718
Copyright
© 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.