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3D-Bioprinted Gelma/Gelatin/Amniotic Membrane Extract (Ame) Scaffold Loaded With Keratinocytes, Fibroblasts, and Endothelial Cells for Skin Tissue Engineering Publisher Pubmed



Pazhouhnia Z1, 2 ; Noori A3 ; Farzin A4 ; Khoshmaram K5 ; Hoseinpour M1 ; Ai J1 ; Ebrahimi M6 ; Lotfibakhshaiesh N1, 7
Authors
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Authors Affiliations
  1. 1. Department of Tissue Engineering, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. AstraBionics Research Network (ARN), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  3. 3. Department of Tissue Engineering and Applied Cell Sciences, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran
  4. 4. Material Engineering Department, Faculty of Engineering, Tarbiat Modares University, Tehran, Iran
  5. 5. Department of Life Science Engineering, Faculty of New Science and Technologies, University of Tehran, Tehran, 1417935840, Iran
  6. 6. Department of Stem Cells and Developmental Biology, Cell Sciences Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
  7. 7. Regenerative Medicine Group (REMED), Universal Scientific Education and Research Network (USERN), Tehran, Iran

Source: Scientific Reports Published:2024


Abstract

Gelatin-methacryloyl (GelMA) is a highly adaptable biomaterial extensively utilized in skin regeneration applications. However, it is frequently imperative to enhance its physical and biological qualities by including supplementary substances in its composition. The purpose of this study was to fabricate and characterize a bi-layered GelMA-gelatin scaffold using 3D bioprinting. The upper section of the scaffold was encompassed with keratinocytes to simulate the epidermis, while the lower section included fibroblasts and HUVEC cells to mimic the dermis. A further step involved the addition of amniotic membrane extract (AME) to the scaffold in order to promote angiogenesis. The incorporation of gelatin into GelMA was found to enhance its stability and mechanical qualities. While the Alamar blue test demonstrated that a high concentration of GelMA (20%) resulted in a decrease in cell viability, the live/dead cell staining revealed that incorporation of AME increased the quantity of viable HUVECs. Further, gelatin upregulated the expression of KRT10 in keratinocytes and VIM in fibroblasts. Additionally, the histological staining results demonstrated the formation of well-defined skin layers and the creation of extracellular matrix (ECM) in GelMA/gelatin hydrogels during a 14-day culture period. Our study showed that a 3D-bioprinted composite scaffold comprising GelMA, gelatin, and AME can be used to regenerate skin tissues. © The Author(s) 2024.
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