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Synthesis of Thermogel Modified With Biomaterials As Carrier for Husscs Differentiation Into Cardiac Cells: Physicomechanical and Biological Assessment Publisher Pubmed



Tapeh SMT1 ; Baei MS1 ; Keshel SH2, 3
Authors
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Authors Affiliations
  1. 1. Department of Chemical Engineering, Ayatollah Amoli Branch, Islamic Azad University, Amol, Iran
  2. 2. Medical Nanotechnology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Department of Tissue Engineering and Applied Cell Science, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Source: Materials Science and Engineering C Published:2021


Abstract

One of the major challenges in cardiac cell therapy is cell death and low rate of cardiac differentiation. In this regard, a series of thermosensitive and injectable hydrogels with similar physicomechanical properties of cardiac tissue can be an ideal candidate for delivering human unrestricted somatic stem cells (hUSSCs) and improve the quality of cell therapy. Here, we designed N-isopropylacrylamide/acrylic acid/N-acryloxysuccinimide/2-hydroxyethyl methacrylate-poly lactide (NIPAAm/AAc/NAS/HEMAPLA) hydrogel via ring-opening polymerization for encapsulation of the cells. To improve biological activities, biomaterials like hyaluronic acid (HA), Aloe vera (AV), and silk fibroin (SF) were added with pure hydrogel (Pgel). The modulus of hydrogels was estimated between 68.1 and 74.63 kPa that was similar to the normal cardiac modulus. Moreover, the elastic region increased by adding biomaterials to Pgel. The results of RT-PCR and ICC demonstrated that the most expression of early genes (GATA4, NKX2.5) was related to Pgel/AV/SF group. In contrast, the highest expression of other genes (GJA1, TNNI3, MYH6) was observed in Pgel/HA/SF. The presence of biomaterials in the structure of hydrogel can play a key role in cell fate and the induction of cell differentiation as a factor influencing mechanotransduction. These hydrogels hold an excellent promise to deliver hUSSCs into damaged tissue for cardiac regeneration. © 2020 Elsevier B.V.
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