Cardiomyocyte differentiation of umbilical cord mesenchymal stem cells on poly(mannitol sebacate)/multi‐walled carbon nanotube substrate

Author:

Hosseinzadeh Elham1,Sigaroodi Faraz2,Ganjoury Camellia3,Parandakh Azim3,Najmoddin Najmeh4ORCID,Shahriari Shayan4,Maymand Maryam Mahmoodinia5,Khani Mohammad‐Mehdi23ORCID

Affiliation:

1. Department of Tissue Engineering, Science and Research Branch Islamic Azad University Tehran Iran

2. Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Technologies in Medicine Shahid Beheshti University of Medical Sciences Tehran Iran

3. Medical Nanotechnology and Tissue Engineering Research Center Shahid Beheshti University of Medical Sciences Tehran Iran

4. Department of Biomedical Engineering, Medical Engineering and Biology Research Center, Science and Research Branch Islamic Azad University Tehran Iran

5. SinaCell Research and Production Co Tehran Iran

Abstract

AbstractMyocardial infarction is one of the main causes of death worldwide. After myocardial infarction, the damaged area is typically occupied with non‐contractile scar tissue owing to the limited ability of cardiac cells to proliferate. Cardiac patches can potentially restore heart function by providing sufficient electrochemical properties to the damaged area and supporting the differentiation into and proliferation of cardiac cells. In this study, we developed for the first time a poly(mannitol sebacate) (PMS) based scaffold combined with 1% (w/w)multi‐walled carbon nanotubes (MWCNTs) to produce a biocompatible cardiac patch by the solvent casting method. We characterized the resultant PMS‐MWCNT scaffold in terms of chemical, physical, mechanical and electrical properties. The PMS/MWCNT patch revealed appropriate hydrophilicity, elasticity close to that of the target tissue, and electrical conductivity suited for a cardiac patch. The cytocompatibility of the composite was confirmed by the successful attachment and proliferation of human umbilical cord mesenchymal stem cells (HUC‐MSCs). The PMS/MWCNTs further contributed to the differentiation of HUC‐MSCs by significant overexpression of cardiac‐specific proteins, i.e. troponin T and connexin 43, in the presence of 5‐azacytidine. The findings of this study could be of assistance in the use and development of PMS‐based composites as cardiac patches for myocardial tissue engineering applications. © 2024 Society of Chemical Industry.

Funder

Shahid Beheshti University of Medical Sciences

Publisher

Wiley

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