4 years ago

Induced Pluripotent Stem Cell (iPSC)-Derived Extracellular Vesicles Are Safer and More Effective for Cardiac Repair than iPSCs.

Magdy Girgis, Urszula Jankowska, Slawomir Lasota, Lin Zhao, Xing Chen, Ewa K Zuba-Surma, Robert J Vincent, Bozena Skupien-Rabian, Anweshan Samanta, Nathaniel Dudley, Ou-Li Wang, Arash Davani, Guangming Cheng, Yu-Ting Xuan, Elzbieta Karnas, Buddhadeb Dawn, Kathy L Newell, Michal Sarna, Sylwia Kedracka-Krok, Zbigniew Madeja, Sylwia Bobis-Wozowicz, Marta Adamiak, Malgorzata Sekula
Rationale: Extracellular vesicles (EVs) are tiny membrane-enclosed droplets released by cells through membrane budding or exocytosis. The myocardial reparative abilities of EVs derived from induced pluripotent stem cells (iPSCs) have not been directly compared with the source iPSCs. Objective: To examine whether iPSC-derived EVs can influence the biological functions of cardiac cells in vitro; and compare the safety and efficacy of iPSC-EVs and iPSCs for cardiac repair in vivo. Methods and Results: Murine iPSCs were generated and EVs isolated from culture supernatants by sequential centrifugation. Atomic force microscopy, high-resolution flow cytometry, real-time qRT-PCR, and mass spectrometry were used to characterize EV morphology and contents. iPSC-EVs were enriched in miRNAs and proteins with proangiogenic and cytoprotective properties. iPSC-EVs enhanced angiogenic, migratory, and antiapoptotic properties of murine cardiac endothelial cells in vitro. To compare the cardiac reparative capacities in vivo, vehicle, iPSCs, and iPSC-EVs were injected intramyocardially at 48 h after a reperfused myocardial infarction in mice. Compared with vehicle-injected mice, both iPSC- and iPSC-EV-treated mice exhibited improved LV function at 35 d after MI, albeit iPSC-EVs rendered greater improvement. iPSC-EV injection also resulted in reduction in LV mass and superior perfusion in the infarct zone. Both iPSCs and iPSC-EVs preserved viable myocardium in the infarct zone, while reduction in apoptosis was significant with iPSC-EVs. iPSC injection resulted in teratoma formation, while iPSC-EV injection was safe. Conclusions: iPSC-derived EVs impart cytoprotective properties to cardiac cells in vitro and induce superior cardiac repair in vivo with regard to LV function, vascularization, and amelioration of apoptosis and hypertrophy. Due to their acellular nature, iPSC-EVs represent a safer alternative for potential therapeutic applications in patients with ischemic myocardial damage.

Publisher URL: http://doi.org/10.1161/CIRCRESAHA.117.311769

DOI: 10.1161/CIRCRESAHA.117.311769

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