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Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing

Chronic wounds have become an increasing medical and economic problem of aging societies because they are difficult to manage. Tissue engineering provides new perspectives for the clinically applicable skin substitutes. Epidermal keratinocytes play an important role in wound epithelization and const...

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Detalles Bibliográficos
Autores principales: Zhang, Xinjian, Xu, Wen, Hu, Xinlei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697525/
https://www.ncbi.nlm.nih.gov/pubmed/34923566
http://dx.doi.org/10.12659/MSM.932978
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author Zhang, Xinjian
Xu, Wen
Hu, Xinlei
author_facet Zhang, Xinjian
Xu, Wen
Hu, Xinlei
author_sort Zhang, Xinjian
collection PubMed
description Chronic wounds have become an increasing medical and economic problem of aging societies because they are difficult to manage. Tissue engineering provides new perspectives for the clinically applicable skin substitutes. Epidermal keratinocytes play an important role in wound epithelization and construction of tissue-engineered skin substitutes. How to obtain a large number of autologous epidermal keratinocytes in a short time is the main problem that limits the application of tissue-engineered skin and epidermal cell membranes. Developing an appropriate method for reproducing the biological potential of cell–cell interactions and simulating the three-dimensional structure between cells has great significance for epidermal keratinocytes expansion and full-thickness skin regeneration. In this article, we propose the concept of tissue-engineered skin regeneration units (TESRUs) as the smallest unit with complete full-thickness skin regeneration ability. First, autologous dermal fibroblasts are cultured in biodegradable macroporous microcarriers to provide the mesenchyme support. Second, autologous epidermal keratinocytes and autologous melanocytes are incubated with the fibroblasts-loaded microcarriers and expand in vitro. Incorporating the above co-culture method into the macroporous microcarriers is reasonable for maintaining cell–cell interactions in spatial and temporal context and providing a suitable growth niche for epidermal keratinocytes. Moreover, TESRUs are composed of fibroblasts, keratinocytes, and melanocytes and have complete full-thickness skin regeneration ability. We suggest that TESRUs could be a promising strategy to repair full-thickness skin defects for clinical applications if the hypothesis proves to be practical.
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spelling pubmed-86975252022-01-10 Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing Zhang, Xinjian Xu, Wen Hu, Xinlei Med Sci Monit Hypothesis Chronic wounds have become an increasing medical and economic problem of aging societies because they are difficult to manage. Tissue engineering provides new perspectives for the clinically applicable skin substitutes. Epidermal keratinocytes play an important role in wound epithelization and construction of tissue-engineered skin substitutes. How to obtain a large number of autologous epidermal keratinocytes in a short time is the main problem that limits the application of tissue-engineered skin and epidermal cell membranes. Developing an appropriate method for reproducing the biological potential of cell–cell interactions and simulating the three-dimensional structure between cells has great significance for epidermal keratinocytes expansion and full-thickness skin regeneration. In this article, we propose the concept of tissue-engineered skin regeneration units (TESRUs) as the smallest unit with complete full-thickness skin regeneration ability. First, autologous dermal fibroblasts are cultured in biodegradable macroporous microcarriers to provide the mesenchyme support. Second, autologous epidermal keratinocytes and autologous melanocytes are incubated with the fibroblasts-loaded microcarriers and expand in vitro. Incorporating the above co-culture method into the macroporous microcarriers is reasonable for maintaining cell–cell interactions in spatial and temporal context and providing a suitable growth niche for epidermal keratinocytes. Moreover, TESRUs are composed of fibroblasts, keratinocytes, and melanocytes and have complete full-thickness skin regeneration ability. We suggest that TESRUs could be a promising strategy to repair full-thickness skin defects for clinical applications if the hypothesis proves to be practical. International Scientific Literature, Inc. 2021-12-19 /pmc/articles/PMC8697525/ /pubmed/34923566 http://dx.doi.org/10.12659/MSM.932978 Text en © Med Sci Monit, 2021 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Hypothesis
Zhang, Xinjian
Xu, Wen
Hu, Xinlei
Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing
title Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing
title_full Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing
title_fullStr Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing
title_full_unstemmed Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing
title_short Tissue-Engineered Skin Regenerative Units for Epidermal Keratinocytes Expansion and Wound Healing
title_sort tissue-engineered skin regenerative units for epidermal keratinocytes expansion and wound healing
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697525/
https://www.ncbi.nlm.nih.gov/pubmed/34923566
http://dx.doi.org/10.12659/MSM.932978
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