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Cellular and Molecular Characterization of Human Cardiac Stem Cells Reveals Key Features Essential for Their Function and Safety Publisher Pubmed



Vahdat S1, 2 ; Mousavi SA3 ; Omrani G4 ; Gholampour M4 ; Sotoodehnejadnematalahi F1 ; Ghazizadeh Z1 ; Gharechahi J3 ; Baharvand H1, 5 ; Salekdeh GH3, 6 ; Aghdami N1, 7
Authors
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Authors Affiliations
  1. 1. Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, PO Box 19395-4644, Acecr, Tehran, 1665659911, Iran
  2. 2. Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran
  3. 3. Department of Molecular Systems Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Acecr, Tehran, Iran
  4. 4. Department of Cardiac Surgery, Rajaei Cardiovascular Medical Research Center, Tehran University of Medical Science, Tehran, Iran
  5. 5. Department of Developmental Biology, University of Science and Culture, Acecr, Tehran, Iran
  6. 6. Department of Systems Biology, Agricultural Biotechnology Research Institute of Iran, Karaj, Iran
  7. 7. Department of Regenerative Biomedicine, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, Acecr, Tehran, Iran

Source: Stem Cells and Development Published:2015


Abstract

Cell therapy of heart diseases is emerging as one of the most promising known treatments in recent years. Transplantation of cardiac stem cells (CSCs) may be one of the best strategies to cure adult or pediatric heart diseases. As these patient-derived stem cells need to be isolated from small heart biopsies, it is important to select the best isolation method and CSC subpopulation with the best cardiogenic functionality. We employed three different protocols including c-KIT+ cell sorting, clonogenic expansion, and explants culture to isolate c-KIT+ cells, clonogenic expansion-derived cells (CEDCs), and cardiosphere-derived cells (CDCs), respectively. Evaluation of isolated CSC characteristics in vitro and after rat myocardial infarction (MI) model transplantation revealed that although c-KIT+ and CDCs had higher MI regenerative potential, CEDCs had more commitment into cardiomyocytes and needed lower passages that were essential to reach a definite cell count. Furthermore, genome-wide expression analysis showed that subsequent passages caused changes in characteristics of cells, downregulation of cell cycle-related genes, and upregulation of differentiation and carcinogenic genes, which might lead to senescence, commitment, and possible tumorigenicity of the cells. Because of different properties of CSC subpopulations, we suggest that appropriate CSCs subpopulation should be chosen based on their experimental or clinical use. © 2015 Mary Ann Liebert, Inc.
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