Mitochondrial Transfer Induced by Adipose-Derived Mesenchymal Stem Cell Transplantation Improves Cardiac Function in Rat Models of Ischemic Cardiomyopathy

Author:

Mori Daisuke1ORCID,Miyagawa Shigeru1,Kawamura Takuji1,Yoshioka Daisuke1,Hata Hiroki1,Ueno Takayoshi1,Toda Koichi1,Kuratani Toru1,Oota Miwa23,Kawai Kotoe23,Kurata Hayato23,Nishida Hiroyuki23,Harada Akima1,Toyofuku Toshihiko4,Sawa Yoshiki15

Affiliation:

1. Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan

2. Institute of Advanced Stem Cell Therapy, Osaka University, Osaka, Japan

3. ROHTO Pharmaceutical Co., Ltd., Osaka, Japan

4. Institute of Immunology and Regenerative Medicine, Osaka University, Osaka, Japan

5. Medical Centre for Translational and Clinical Research, Osaka University Hospital, Osaka, Japan

Abstract

Although mesenchymal stem cell transplantation has been successful in the treatment of ischemic cardiomyopathy, the underlying mechanisms remain unclear. Herein, we investigated whether mitochondrial transfer could explain the success of cell therapy in ischemic cardiomyopathy. Mitochondrial transfer in co-cultures of human adipose-derived mesenchymal stem cells and rat cardiomyocytes maintained under hypoxic conditions was examined. Functional recovery was monitored in a rat model of myocardial infarction following human adipose-derived mesenchymal stem cell transplantation. We observed mitochondrial transfer in vitro, which required the formation of cell-to-cell contacts and synergistically enhanced energy metabolism. Rat cardiomyocytes exhibited mitochondrial transfer 3 days following human adipose-derived mesenchymal stem cell transplantation to the ischemic heart surface post-myocardial infarction. We detected donor mitochondrial DNA in the recipient myocardium concomitant with a significant improvement in cardiac function. Mitochondrial transfer is vital for successful cell transplantation therapies and improves treatment outcomes in ischemic cardiomyopathy.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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