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Efficient Cardiomyocyte Differentiation of Induced Pluripotent Stem Cells on Plga Nanofibers Enriched by Platelet-Rich Plasma Publisher



Torabi M1 ; Abazari MF2 ; Zare Karizi S3 ; Kohandani M4 ; Hajatibirgani N5 ; Norouzi S5 ; Nejati F6 ; Mohajerani A7 ; Rahmati T8 ; Mokhames Z9
Authors
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Authors Affiliations
  1. 1. Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran
  2. 2. Research Center for Clinical Virology, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Biology, Varamin Pishva Branch, Islamic Azad University, Pishva, Iran
  4. 4. Department of Biology, Faculty of Biological Sciences, Islamic Azad University, East Tehran Branch, Tehran, Iran
  5. 5. Department of Biology, Faculty of Science and Research, Islamic Azad University, Tehran, Iran
  6. 6. Institute of Molecular Biology, Vrije Universiteit Brussel, Brussels, Belgium
  7. 7. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. SinaCell Research and Product Center, Pardis Technology Park, Tehran, Iran
  9. 9. Department of Molecular Diagnostic, Emam Ali Educational and Therapeutic Center, Alborz University of Medical Sciences, Karaj, Iran

Source: Polymers for Advanced Technologies Published:2021


Abstract

Regeneration and restoring the function of the myocardial-infracted hearts have been one of the constant challenges in medicine. Recently, tissue engineering, using biocompatible substrates and stem cells, holds a real promise to solve these problems. Herein, poly(lactic-co-glycolic acid) (PLGA) nanofibers and platelet-rich plasma (PRP) enriched PLGA nanofibers (PLGA-PRP) were fabricated by electrospinning. Scanning electron microscopy (SEM) demonstrated that fiber diameters in PLGA scaffolds with and without PRP were in the range of 500 ± 280 nm and fibers were also bead free, smooth, in random orientation, and with interconnected pores. During culture of the human-induced pluripotent stem cells (iPSCs) on the nanofibrous scaffold, further differentiation of the iPSCs to cardiomyocytes was detected in PLGA-PRP nanofibers compared to the PLGA. This improvement in differentiation potential was evaluated at the morphological, molecular gene, and protein expression levels using SEM, real-time reverse transcription-polymerase chain reaction (RT-PCR), and immunocytochemistry, respectively. The results obtained in this study highlighted the significance of natural growth factors present in the artificial scaffold applied in cardiac tissue engineering according to the improvements in cell-biomaterial interactions. Taken together, our result indicated that PRP-incorporated PLGA could be considered as a great potential candidate to use for engineering suitable myocardium replacement constructs. © 2020 John Wiley & Sons Ltd