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Comparative Effectiveness of Three-Dimensional Scaffold, Differentiation Media and Co-Culture With Native Cardiomyocytes to Trigger in Vitro Cardiogenic Differentiation of Menstrual Blood and Bone Marrow Stem Cells Publisher Pubmed



Rahimi M1, 2 ; Zarnani AH3, 4 ; Mobini S5 ; Khorasani S6 ; Darzi M6 ; Kazemnejad S6
Authors
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Authors Affiliations
  1. 1. Department of Biology, Faculty of Sciences, Malayer University, Malayer, Iran
  2. 2. Department of Animal Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran
  3. 3. Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Reproductive Immunology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran
  5. 5. Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran
  6. 6. Nanobiotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran

Source: Biologicals Published:2018


Abstract

The main purpose of this study was to find effectiveness of 3D silk fibroin scaffold in comparison with co-culturing in presence of native cardiomyocytes on cardiac differentiation propensity of menstural blood(MenSCs)-versus bone marrow-derived stem-cells (BMSCs). We showed that both 3D fibroin scaffold and co-culture system supported efficient cardiomyogenic differentiation of MenSCs and BMSCs, as judged by the expression of cardiac-specific genes and proteins, Connexin-43, Connexin-40, alpha Actinin (ACTN-2), Tropomyosin1 (TPM1) and Cardiac Troponin T (TNNT2). No significant difference (except for higher expression of ACTN-2 in co-cultured MenSCs) was found between differentiation potential of the cells cultured in 3D fibroin scaffold and co-culture system. Collectively, our results imply that inductive signals served by biological factors of native cardiomyocytes to trigger cardiogenic differentiation of stem-cells may be efficiently provided by natural and biocompatible 3D fibroin scaffold suggesting the usefulness of this construct for cardiac tissue engineering. © 2018
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