期刊
INTERNATIONAL JOURNAL OF CARDIOLOGY
卷 182, 期 -, 页码 349-360出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2014.12.043
关键词
Exosomes; MiR transfer; Target proteins; Bone marrow stem cells; Cardioprotection; GATA-4
资金
- National Institutes of Health [HL105176, HL114654, R37HL 074272]
Background: Exosomes play an important role in intercellular signaling and exert regulatory function by carrying bioactive molecules. This study investigated (1) the cardioprotective capabilities of exosomes derived from mesenchymal stemcells (MSCs) overexpressing GATA-4 (MSCGATA-4) and (2) its underlying regulatory mechanisms for expression of target proteins in recipient cells. Methods and results: Exosomes were isolated and purified from MSCGATA-4 (Exo(GATA-4)) and control MSCs (Exo(Null)). Cell injury was investigated in primary cultured rat neonatal cardiomyocytes (CM) and in the rat heart. Exosomes contributed to increased CM survival, reduced CM apoptosis, and preserved mitochondrial membrane potential in CM cultured under a hypoxic environment. Direct intramyocardial transplantation of exosomes at the border of an ischemic region following ligation of the left anterior descending coronary artery significantly restored cardiac contractile function and reduced infarct size. Real-time PCR revealed that several anti-apoptotic miRs were highly expressed in Exo(GATA-4). Rapid internalization of Exo(GATA-4) by CM was documented using time-lapse imaging. Subsequent expression of these miRs, particularly miR-19a was higher in CM and in the myocardium treated with Exo(GATA-4) compared to those treated with Exo(Null). The enhanced protective effects observed in CM were diminished by the inhibition of miR-19a. The expression level of PTEN, a predicted target of miR-19a, was reduced in CM treated with Exo(GATA-4), which resulted in the activation of the Akt and ERK signaling pathways. Conclusions: Exo(GATA-4) upon transplantation in the damaged tissue mediate protection by releasing multiple miRs responsible for activation of the cell survival signaling pathway. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
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