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Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel

Skin substitutes with existing vascularization are in great demand for the repair of full-thickness skin defects. In the present study, we hypothesized that a pre-vascularized skin substitute can potentially promote wound healing. Novel three-dimensional (3D) skin substitutes were prepared by seedin...

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Autores principales: Dai, Niann-Tzyy, Huang, Wen-Shyan, Chang, Fang-Wei, Wei, Lin-Gwei, Huang, Tai-Chun, Li, Jhen-Kai, Fu, Keng-Yen, Dai, Lien-Guo, Hsieh, Pai-Shan, Huang, Nien-Chi, Wang, Yi-Wen, Chang, Hsin-I, Parungao, Roxanne, Wang, Yiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180730/
https://www.ncbi.nlm.nih.gov/pubmed/30203684
http://dx.doi.org/10.1177/0963689718797570
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author Dai, Niann-Tzyy
Huang, Wen-Shyan
Chang, Fang-Wei
Wei, Lin-Gwei
Huang, Tai-Chun
Li, Jhen-Kai
Fu, Keng-Yen
Dai, Lien-Guo
Hsieh, Pai-Shan
Huang, Nien-Chi
Wang, Yi-Wen
Chang, Hsin-I
Parungao, Roxanne
Wang, Yiwei
author_facet Dai, Niann-Tzyy
Huang, Wen-Shyan
Chang, Fang-Wei
Wei, Lin-Gwei
Huang, Tai-Chun
Li, Jhen-Kai
Fu, Keng-Yen
Dai, Lien-Guo
Hsieh, Pai-Shan
Huang, Nien-Chi
Wang, Yi-Wen
Chang, Hsin-I
Parungao, Roxanne
Wang, Yiwei
author_sort Dai, Niann-Tzyy
collection PubMed
description Skin substitutes with existing vascularization are in great demand for the repair of full-thickness skin defects. In the present study, we hypothesized that a pre-vascularized skin substitute can potentially promote wound healing. Novel three-dimensional (3D) skin substitutes were prepared by seeding a mixture of human endothelial progenitor cells (EPCs) and fibroblasts into a human plasma/calcium chloride formed gel scaffold, and seeding keratinocytes onto the surface of the plasma gel. The capacity of the EPCs to differentiate into a vascular-like tubular structure was evaluated using immunohistochemistry analysis and WST-8 assay. Experimental studies in mouse full-thickness skin wound models showed that the pre-vascularized gel scaffold significantly accelerated wound healing 7 days after surgery, and resembled normal skin structures after 14 days post-surgery. Histological analysis revealed that pre-vascularized gel scaffolds were well integrated in the host skin, resulting in the vascularization of both the epidermis and dermis in the wound area. Moreover, mechanical strength analysis demonstrated that the healed wound following the implantation of the pre-vascularized gel scaffolds exhibited good tensile strength. Taken together, this novel pre-vascularized human plasma gel scaffold has great potential in skin tissue engineering.
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spelling pubmed-61807302018-10-19 Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel Dai, Niann-Tzyy Huang, Wen-Shyan Chang, Fang-Wei Wei, Lin-Gwei Huang, Tai-Chun Li, Jhen-Kai Fu, Keng-Yen Dai, Lien-Guo Hsieh, Pai-Shan Huang, Nien-Chi Wang, Yi-Wen Chang, Hsin-I Parungao, Roxanne Wang, Yiwei Cell Transplant Original Articles Skin substitutes with existing vascularization are in great demand for the repair of full-thickness skin defects. In the present study, we hypothesized that a pre-vascularized skin substitute can potentially promote wound healing. Novel three-dimensional (3D) skin substitutes were prepared by seeding a mixture of human endothelial progenitor cells (EPCs) and fibroblasts into a human plasma/calcium chloride formed gel scaffold, and seeding keratinocytes onto the surface of the plasma gel. The capacity of the EPCs to differentiate into a vascular-like tubular structure was evaluated using immunohistochemistry analysis and WST-8 assay. Experimental studies in mouse full-thickness skin wound models showed that the pre-vascularized gel scaffold significantly accelerated wound healing 7 days after surgery, and resembled normal skin structures after 14 days post-surgery. Histological analysis revealed that pre-vascularized gel scaffolds were well integrated in the host skin, resulting in the vascularization of both the epidermis and dermis in the wound area. Moreover, mechanical strength analysis demonstrated that the healed wound following the implantation of the pre-vascularized gel scaffolds exhibited good tensile strength. Taken together, this novel pre-vascularized human plasma gel scaffold has great potential in skin tissue engineering. SAGE Publications 2018-09-11 2018-10 /pmc/articles/PMC6180730/ /pubmed/30203684 http://dx.doi.org/10.1177/0963689718797570 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Dai, Niann-Tzyy
Huang, Wen-Shyan
Chang, Fang-Wei
Wei, Lin-Gwei
Huang, Tai-Chun
Li, Jhen-Kai
Fu, Keng-Yen
Dai, Lien-Guo
Hsieh, Pai-Shan
Huang, Nien-Chi
Wang, Yi-Wen
Chang, Hsin-I
Parungao, Roxanne
Wang, Yiwei
Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel
title Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel
title_full Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel
title_fullStr Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel
title_full_unstemmed Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel
title_short Development of a Novel Pre-Vascularized Three-Dimensional Skin Substitute Using Blood Plasma Gel
title_sort development of a novel pre-vascularized three-dimensional skin substitute using blood plasma gel
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180730/
https://www.ncbi.nlm.nih.gov/pubmed/30203684
http://dx.doi.org/10.1177/0963689718797570
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