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A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing

BACKGROUND: Diabetic wound is a severe complication of diabetes. Stem cell is considered as a promising therapy for diabetic skin wounds. Hydrogel can supply niche for cells adhesion and survival to improve the efficacy of stem cell therapy, but the development of hydrogel with suitable properties r...

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Autores principales: Xu, Hongjie, Wang, Jingjing, Wu, Di, Qin, Dajiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293866/
https://www.ncbi.nlm.nih.gov/pubmed/35849219
http://dx.doi.org/10.1007/s10856-022-06681-4
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author Xu, Hongjie
Wang, Jingjing
Wu, Di
Qin, Dajiang
author_facet Xu, Hongjie
Wang, Jingjing
Wu, Di
Qin, Dajiang
author_sort Xu, Hongjie
collection PubMed
description BACKGROUND: Diabetic wound is a severe complication of diabetes. Stem cell is considered as a promising therapy for diabetic skin wounds. Hydrogel can supply niche for cells adhesion and survival to improve the efficacy of stem cell therapy, but the development of hydrogel with suitable properties remains a great challenge. Thus, our study was conducted to combine an optimized hydrogel with stem cell to improve complex diabetic wound treatment. METHODS: This study constructed a hydrogel with low toxicity and adjustable mechanical properties from gelatin methacrylate (GelMA) and chitosan-catechol (Chi-C), and encapsulated human umbilical cord-mesenchymal stem cells (hUMSCs) to repair full-thickness diabetic wound. RESULTS: We explored the relationship between mechanical stiffness and cell proliferation and differentiation potency, and found 10% GelMA hydrogel with an optimal stiffness improved hUMSCs adhesion, proliferation, and differentiation potency maintenance in vitro. Assistant with optimized hydrogel encapsulating hUMSCs, diabetic wound healing process was greatly accelerated, including accelerated wound closure, inhibited secretion of inflammatory factors TNF-α and IL-1β, promoted vascular regeneration and collagen deposition after treatment of hUMSCs. CONCLUSIONS: The optimized hydrogel encapsulating hUMSCs improved diabetic wound healing, and has a broad implication for the treatment of diabetic complication. [Figure: see text]
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spelling pubmed-92938662022-07-20 A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing Xu, Hongjie Wang, Jingjing Wu, Di Qin, Dajiang J Mater Sci Mater Med Tissue Engineering Constructs and Cell Substrates BACKGROUND: Diabetic wound is a severe complication of diabetes. Stem cell is considered as a promising therapy for diabetic skin wounds. Hydrogel can supply niche for cells adhesion and survival to improve the efficacy of stem cell therapy, but the development of hydrogel with suitable properties remains a great challenge. Thus, our study was conducted to combine an optimized hydrogel with stem cell to improve complex diabetic wound treatment. METHODS: This study constructed a hydrogel with low toxicity and adjustable mechanical properties from gelatin methacrylate (GelMA) and chitosan-catechol (Chi-C), and encapsulated human umbilical cord-mesenchymal stem cells (hUMSCs) to repair full-thickness diabetic wound. RESULTS: We explored the relationship between mechanical stiffness and cell proliferation and differentiation potency, and found 10% GelMA hydrogel with an optimal stiffness improved hUMSCs adhesion, proliferation, and differentiation potency maintenance in vitro. Assistant with optimized hydrogel encapsulating hUMSCs, diabetic wound healing process was greatly accelerated, including accelerated wound closure, inhibited secretion of inflammatory factors TNF-α and IL-1β, promoted vascular regeneration and collagen deposition after treatment of hUMSCs. CONCLUSIONS: The optimized hydrogel encapsulating hUMSCs improved diabetic wound healing, and has a broad implication for the treatment of diabetic complication. [Figure: see text] Springer US 2022-07-18 2022 /pmc/articles/PMC9293866/ /pubmed/35849219 http://dx.doi.org/10.1007/s10856-022-06681-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Tissue Engineering Constructs and Cell Substrates
Xu, Hongjie
Wang, Jingjing
Wu, Di
Qin, Dajiang
A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
title A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
title_full A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
title_fullStr A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
title_full_unstemmed A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
title_short A hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
title_sort hybrid hydrogel encapsulating human umbilical cord mesenchymal stem cells enhances diabetic wound healing
topic Tissue Engineering Constructs and Cell Substrates
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293866/
https://www.ncbi.nlm.nih.gov/pubmed/35849219
http://dx.doi.org/10.1007/s10856-022-06681-4
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