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Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts
The skin is the largest human organ, and defects in the skin with a diameter greater than 4 cm do not heal without treatment. Allogeneic skin transplantation has been used to allow wound healing, but many grafts do not survive after implantation, due to multiple complications in the procedure. In th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Whioce Publishing Pte. Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294694/ https://www.ncbi.nlm.nih.gov/pubmed/32596551 http://dx.doi.org/10.18063/ijb.v6i1.246 |
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author | Huyan, Yige Lian, Qin Zhao, Tingze Li, Dichen He, Jiankang |
author_facet | Huyan, Yige Lian, Qin Zhao, Tingze Li, Dichen He, Jiankang |
author_sort | Huyan, Yige |
collection | PubMed |
description | The skin is the largest human organ, and defects in the skin with a diameter greater than 4 cm do not heal without treatment. Allogeneic skin transplantation has been used to allow wound healing, but many grafts do not survive after implantation, due to multiple complications in the procedure. In the present study, the vascularization of three-dimensional (3D) printed full-thickness skin grafts was investigated. Dermal-epithelial grafts were transplanted into a nude mouse model to evaluate integration with the host tissue and the extent of wound healing. To create microvessels in the skin grafts, a bilayer structure consisting of human dermal fibroblasts, keratinocytes, and microvascular endothelial cells was designed and fabricated using an extruded 3D printer. Human dermal fibroblasts and human microvascular endothelial cells were mixed with gelatin-sodium alginate composite hydrogel as the dermis, and human keratinocytes were mixed with gel as the epithelium. Confocal imaging allowed visualization of the location of the cells in the double-layer skin grafts. A full-thickness wound was created on the backs of nude mice and then covered with a double-layer skin graft. Various groups of mice were tested. Animals were euthanized and tissue samples collected after specified time points. Compared with the control group, wound contraction improved by approximately 10%. Histological analysis demonstrated that the new skin had an appearance similar to that of normal skin and with a significant degree of angiogenesis. The results of the immunohistochemical analysis demonstrated that the transplanted cells survived and participated in the healing process. |
format | Online Article Text |
id | pubmed-7294694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Whioce Publishing Pte. Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72946942020-06-25 Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts Huyan, Yige Lian, Qin Zhao, Tingze Li, Dichen He, Jiankang Int J Bioprint Research Article The skin is the largest human organ, and defects in the skin with a diameter greater than 4 cm do not heal without treatment. Allogeneic skin transplantation has been used to allow wound healing, but many grafts do not survive after implantation, due to multiple complications in the procedure. In the present study, the vascularization of three-dimensional (3D) printed full-thickness skin grafts was investigated. Dermal-epithelial grafts were transplanted into a nude mouse model to evaluate integration with the host tissue and the extent of wound healing. To create microvessels in the skin grafts, a bilayer structure consisting of human dermal fibroblasts, keratinocytes, and microvascular endothelial cells was designed and fabricated using an extruded 3D printer. Human dermal fibroblasts and human microvascular endothelial cells were mixed with gelatin-sodium alginate composite hydrogel as the dermis, and human keratinocytes were mixed with gel as the epithelium. Confocal imaging allowed visualization of the location of the cells in the double-layer skin grafts. A full-thickness wound was created on the backs of nude mice and then covered with a double-layer skin graft. Various groups of mice were tested. Animals were euthanized and tissue samples collected after specified time points. Compared with the control group, wound contraction improved by approximately 10%. Histological analysis demonstrated that the new skin had an appearance similar to that of normal skin and with a significant degree of angiogenesis. The results of the immunohistochemical analysis demonstrated that the transplanted cells survived and participated in the healing process. Whioce Publishing Pte. Ltd. 2020-01-21 /pmc/articles/PMC7294694/ /pubmed/32596551 http://dx.doi.org/10.18063/ijb.v6i1.246 Text en Copyright © 2020, Whioce Publishing Pte. Ltd. http://creativecommons.org/licenses/cc-by-nc/4.0/ This is an open-access article distributed under the terms of the Attribution-NonCommercial 4.0 International 4.0 (CC BY-NC 4.0), which permits all non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited. |
spellingShingle | Research Article Huyan, Yige Lian, Qin Zhao, Tingze Li, Dichen He, Jiankang Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts |
title | Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts |
title_full | Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts |
title_fullStr | Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts |
title_full_unstemmed | Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts |
title_short | Pilot Study of the Biological Properties and Vascularization of 3D Printed Bilayer Skin Grafts |
title_sort | pilot study of the biological properties and vascularization of 3d printed bilayer skin grafts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294694/ https://www.ncbi.nlm.nih.gov/pubmed/32596551 http://dx.doi.org/10.18063/ijb.v6i1.246 |
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