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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...

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Autores principales: Baltazar, Tania, Jiang, Bo, Moncayo, Alejandra, Merola, Jonathan, Albanna, Mohammad Z., Saltzman, W. Mark, Pober, Jordan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
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.
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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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