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Combining Mesenchymal Stem Cells Derived from Wharton’s Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery
[Image: see text] Therapies based on mesenchymal stem cells have incredible potential for tissue regeneration. Tracking cells and keeping them at the injury site are creating challenges. The cells can be sown into a biocompatible scaffold as a possible remedy. Tissue engineering construction is a di...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339331/ https://www.ncbi.nlm.nih.gov/pubmed/37457470 http://dx.doi.org/10.1021/acsomega.3c01689 |
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author | Palaniappan, Umamagesh Kannaiyan, Jaianand Paulraj, Balaji Karuppiah, Ponmurugan Basavarajappa, Santhosh Syed, Asad Elgorban, Abdallah M. Zaghloul, Nouf S. Veeramanikandan, Veeramani |
author_facet | Palaniappan, Umamagesh Kannaiyan, Jaianand Paulraj, Balaji Karuppiah, Ponmurugan Basavarajappa, Santhosh Syed, Asad Elgorban, Abdallah M. Zaghloul, Nouf S. Veeramanikandan, Veeramani |
author_sort | Palaniappan, Umamagesh |
collection | PubMed |
description | [Image: see text] Therapies based on mesenchymal stem cells have incredible potential for tissue regeneration. Tracking cells and keeping them at the injury site are creating challenges. The cells can be sown into a biocompatible scaffold as a possible remedy. Tissue engineering construction is a difficult, multistep process that requires many variables to be optimized, including the stem cell source, molecular components, scaffold architecture, and a suitable in vivo animal model. In order to locate a suitable regenerative scaffold for delivering stromal cells to regions with greater healing potential, we assessed whether human Wharton’s Jelly-derived mesenchymal stem cells (WJMSCs) responded on biological membranes. WJMSCs were isolated, characterized, and seeded onto an amniotic membrane-based scaffold. Results obtained in vitro revealed that the seeded scaffolds had a significant impact on a number of critical variables, including seeding effectiveness, cellular dispersion, adhesion, survival, and metabolic activity. The research sheds light on a fresh facet of material behavior and paves the way for the creation of scaffold materials that support tissue regeneration and repair. Furthermore, the methods used herein can be utilized to test other scaffold materials to increase their healing potential with WJMSCs. |
format | Online Article Text |
id | pubmed-10339331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-103393312023-07-14 Combining Mesenchymal Stem Cells Derived from Wharton’s Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery Palaniappan, Umamagesh Kannaiyan, Jaianand Paulraj, Balaji Karuppiah, Ponmurugan Basavarajappa, Santhosh Syed, Asad Elgorban, Abdallah M. Zaghloul, Nouf S. Veeramanikandan, Veeramani ACS Omega [Image: see text] Therapies based on mesenchymal stem cells have incredible potential for tissue regeneration. Tracking cells and keeping them at the injury site are creating challenges. The cells can be sown into a biocompatible scaffold as a possible remedy. Tissue engineering construction is a difficult, multistep process that requires many variables to be optimized, including the stem cell source, molecular components, scaffold architecture, and a suitable in vivo animal model. In order to locate a suitable regenerative scaffold for delivering stromal cells to regions with greater healing potential, we assessed whether human Wharton’s Jelly-derived mesenchymal stem cells (WJMSCs) responded on biological membranes. WJMSCs were isolated, characterized, and seeded onto an amniotic membrane-based scaffold. Results obtained in vitro revealed that the seeded scaffolds had a significant impact on a number of critical variables, including seeding effectiveness, cellular dispersion, adhesion, survival, and metabolic activity. The research sheds light on a fresh facet of material behavior and paves the way for the creation of scaffold materials that support tissue regeneration and repair. Furthermore, the methods used herein can be utilized to test other scaffold materials to increase their healing potential with WJMSCs. American Chemical Society 2023-06-27 /pmc/articles/PMC10339331/ /pubmed/37457470 http://dx.doi.org/10.1021/acsomega.3c01689 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Palaniappan, Umamagesh Kannaiyan, Jaianand Paulraj, Balaji Karuppiah, Ponmurugan Basavarajappa, Santhosh Syed, Asad Elgorban, Abdallah M. Zaghloul, Nouf S. Veeramanikandan, Veeramani Combining Mesenchymal Stem Cells Derived from Wharton’s Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery |
title | Combining Mesenchymal
Stem Cells Derived from Wharton’s
Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery |
title_full | Combining Mesenchymal
Stem Cells Derived from Wharton’s
Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery |
title_fullStr | Combining Mesenchymal
Stem Cells Derived from Wharton’s
Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery |
title_full_unstemmed | Combining Mesenchymal
Stem Cells Derived from Wharton’s
Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery |
title_short | Combining Mesenchymal
Stem Cells Derived from Wharton’s
Jelly and Amniotic Biomaterial Scaffolds for Cell Delivery |
title_sort | combining mesenchymal
stem cells derived from wharton’s
jelly and amniotic biomaterial scaffolds for cell delivery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339331/ https://www.ncbi.nlm.nih.gov/pubmed/37457470 http://dx.doi.org/10.1021/acsomega.3c01689 |
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