Hepatoma-Derived Growth Factor Secreted from Mesenchymal Stem Cells Reduces Myocardial Ischemia-Reperfusion Injury. (14th November 2017)

• Record Type: Journal Article
• Authors: Zhou, Yu; Chen, Panpan; Liu, Qingnian; Wang, Yingchao; Zhang, Ling; Wu, Rongrong; Chen, Jinghai; Yu, Hong; Zhu, Wei; Hu, Xinyang; Wang, Jian-An
• Other Names: Chen Yanfang Academic Editor.
• Is Part Of: Stem cells international. Volume 2017(2017)
• Publication Date: 2017-11-14
• Subjects: Stem Cells -- Periodicals; Stem Cells -- Therapeutic use -- Periodicals; Stem Cells -- Transplantation -- Periodicals; 616.0277405
• DOI: 10.1155/2017/1096980
• Languages: English
• ISSNs: 1687-966X

Abstract

Abstract : Objectives . The present study aimed to explore the major factors that account for the beneficial effects of mesenchymal stem cells (MSCs). Methods . Using isobaric tags for relative and absolute quantitation method, hepatoma-derived growth factor (HDGF) was identified as an important factor secreted by MSCs, but not by cardiac fibroblasts (CFs). The protective effects of conditioned medium (CdM) from MSCs or CFs were tested by using either H9C2 cells that were exposed by hypoxia-reoxygenation (H/R) insult or an in vivo mouse model of myocardial ischemia-reperfusion. Results . Compared to CF-CdM, MSC-CdM conferred protection against reperfusion injury. CdM obtained from MSCs that were treated with HDGF-targeted shRNA failed to offer any protection in vitro . In addition, administration of recombinant HDGF alone recapitulated the beneficial effects of MSC-CdM, which was associated with increased protein kinase C epsilon (PKC ε ) phosphorylation, enhanced mitochondria aldehyde dehydrogenase family 2 activity, and decreased 4-hydroxy-2-nonenal accumulation. A significant decrease in infarct size and ameliorated cardiac dysfunction was achieved by administration of HDGF in wild-type mice, which was absent in PKC ε dominant negative mice, indicating the essential roles of PKC ε in HDGF-mediated protection. Conclusions . HDGF secreted from MSCs plays a key role in the protection against reperfusion injury through PKC ε activation.