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Comparison of Non-human Primate versus Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Treatment of Myocardial Infarction

Non-human primates (NHPs) can serve as a human-like model to study cell therapy using induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs). However, whether the efficacy of NHP and human iPSC-CMs is mechanistically similar remains unknown. To examine this, RNU rats received intramyocardia...

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Detalles Bibliográficos
Autores principales: Zhao, Xin, Chen, Haodong, Xiao, Dan, Yang, Huaxiao, Itzhaki, Ilanit, Qin, Xulei, Chour, Tony, Aguirre, Aitor, Lehmann, Kim, Kim, Youngkyun, Shukla, Praveen, Holmström, Alexandra, Zhang, Joe Z., Zhuge, Yan, Ndoye, Babacar C., Zhao, Mingtao, Neofytou, Evgenios, Zimmermann, Wolfram-Hubertus, Jain, Mohit, Wu, Joseph C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830958/
https://www.ncbi.nlm.nih.gov/pubmed/29398480
http://dx.doi.org/10.1016/j.stemcr.2018.01.002
Descripción
Sumario:Non-human primates (NHPs) can serve as a human-like model to study cell therapy using induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs). However, whether the efficacy of NHP and human iPSC-CMs is mechanistically similar remains unknown. To examine this, RNU rats received intramyocardial injection of 1 × 10(7) NHP or human iPSC-CMs or the same number of respective fibroblasts or PBS control (n = 9–14/group) at 4 days after 60-min coronary artery occlusion-reperfusion. Cardiac function and left ventricular remodeling were similarly improved in both iPSC-CM-treated groups. To mimic the ischemic environment in the infarcted heart, both cultured NHP and human iPSC-CMs underwent 24-hr hypoxia in vitro. Both cells and media were collected, and similarities in transcriptomic as well as metabolomic profiles were noted between both groups. In conclusion, both NHP and human iPSC-CMs confer similar cardioprotection in a rodent myocardial infarction model through relatively similar mechanisms via promotion of cell survival, angiogenesis, and inhibition of hypertrophy and fibrosis.