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3D bioprinting of an implantable xeno‐free vascularized human skin graft
Bioengineered tissues or organs produced using matrix proteins or components derived from xenogeneic sources pose risks of allergic responses, immune rejection, or even autoimmunity. Here, we report successful xeno‐free isolation, expansion, and cryopreservation of human endothelial cells (EC), fibr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842062/ https://www.ncbi.nlm.nih.gov/pubmed/36684084 http://dx.doi.org/10.1002/btm2.10324 |
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author | Baltazar, Tania Jiang, Bo Moncayo, Alejandra Merola, Jonathan Albanna, Mohammad Z. Saltzman, W. Mark Pober, Jordan S. |
author_facet | Baltazar, Tania Jiang, Bo Moncayo, Alejandra Merola, Jonathan Albanna, Mohammad Z. Saltzman, W. Mark Pober, Jordan S. |
author_sort | Baltazar, Tania |
collection | PubMed |
description | Bioengineered tissues or organs produced using matrix proteins or components derived from xenogeneic sources pose risks of allergic responses, immune rejection, or even autoimmunity. Here, we report successful xeno‐free isolation, expansion, and cryopreservation of human endothelial cells (EC), fibroblasts (FBs), pericytes (PCs), and keratinocytes (KCs). We further demonstrate the bioprinting of a human skin substitute with a dermal layer containing xeno‐free cultured human EC, FBs, and PCs in a xeno‐free bioink containing human collagen type I and fibronectin layered in a biocompatible polyglycolic acid mesh and subsequently seeded with xeno‐free human KCs to form an epidermal layer. Following implantation of such bilayered skin grafts on the dorsum of immunodeficient mice, KCs form a mature stratified epidermis with rete ridge‐like structures. The ECs and PCs form human EC‐lined perfused microvessels within 2 weeks after implantation, preventing graft necrosis, and eliciting further perfusion of the graft by angiogenic host microvessels. As proof‐of‐concept, we generated 12 individual grafts using a single donor of all four cell types. In summary, we describe the fabrication of a bioprinted vascularized bilayered skin substitute under completely xeno‐free culture conditions demonstrating feasibility of a xeno‐free approach to complex tissue engineering. |
format | Online Article Text |
id | pubmed-9842062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98420622023-01-19 3D bioprinting of an implantable xeno‐free vascularized human skin graft Baltazar, Tania Jiang, Bo Moncayo, Alejandra Merola, Jonathan Albanna, Mohammad Z. Saltzman, W. Mark Pober, Jordan S. Bioeng Transl Med Research Articles Bioengineered tissues or organs produced using matrix proteins or components derived from xenogeneic sources pose risks of allergic responses, immune rejection, or even autoimmunity. Here, we report successful xeno‐free isolation, expansion, and cryopreservation of human endothelial cells (EC), fibroblasts (FBs), pericytes (PCs), and keratinocytes (KCs). We further demonstrate the bioprinting of a human skin substitute with a dermal layer containing xeno‐free cultured human EC, FBs, and PCs in a xeno‐free bioink containing human collagen type I and fibronectin layered in a biocompatible polyglycolic acid mesh and subsequently seeded with xeno‐free human KCs to form an epidermal layer. Following implantation of such bilayered skin grafts on the dorsum of immunodeficient mice, KCs form a mature stratified epidermis with rete ridge‐like structures. The ECs and PCs form human EC‐lined perfused microvessels within 2 weeks after implantation, preventing graft necrosis, and eliciting further perfusion of the graft by angiogenic host microvessels. As proof‐of‐concept, we generated 12 individual grafts using a single donor of all four cell types. In summary, we describe the fabrication of a bioprinted vascularized bilayered skin substitute under completely xeno‐free culture conditions demonstrating feasibility of a xeno‐free approach to complex tissue engineering. John Wiley & Sons, Inc. 2022-04-21 /pmc/articles/PMC9842062/ /pubmed/36684084 http://dx.doi.org/10.1002/btm2.10324 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Baltazar, Tania Jiang, Bo Moncayo, Alejandra Merola, Jonathan Albanna, Mohammad Z. Saltzman, W. Mark Pober, Jordan S. 3D bioprinting of an implantable xeno‐free vascularized human skin graft |
title |
3D bioprinting of an implantable xeno‐free vascularized human skin graft |
title_full |
3D bioprinting of an implantable xeno‐free vascularized human skin graft |
title_fullStr |
3D bioprinting of an implantable xeno‐free vascularized human skin graft |
title_full_unstemmed |
3D bioprinting of an implantable xeno‐free vascularized human skin graft |
title_short |
3D bioprinting of an implantable xeno‐free vascularized human skin graft |
title_sort | 3d bioprinting of an implantable xeno‐free vascularized human skin graft |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842062/ https://www.ncbi.nlm.nih.gov/pubmed/36684084 http://dx.doi.org/10.1002/btm2.10324 |
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