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Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model
Tissue‐engineered skin constructs, including bi‐layered living cellular constructs (BLCC) used in the treatment of chronic wounds, are structurally/functionally complex. While some work has been performed to understand their mechanisms, the totality of how BLCC may function in wound healing remains...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885468/ https://www.ncbi.nlm.nih.gov/pubmed/35918057 http://dx.doi.org/10.1111/iwj.13889 |
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author | Avery, Justin T. Qiao, Jizeng Medeiros, Erika Bollenbach, Thomas J. Kimmerling, Kelly A. Mowry, Katie C. |
author_facet | Avery, Justin T. Qiao, Jizeng Medeiros, Erika Bollenbach, Thomas J. Kimmerling, Kelly A. Mowry, Katie C. |
author_sort | Avery, Justin T. |
collection | PubMed |
description | Tissue‐engineered skin constructs, including bi‐layered living cellular constructs (BLCC) used in the treatment of chronic wounds, are structurally/functionally complex. While some work has been performed to understand their mechanisms, the totality of how BLCC may function in wound healing remains unknown. To this end, we have developed a delayed wound healing model to test BLCC cellular and molecular mechanisms of action. Diabetes was chemically‐induced using alloxan in Yucatan miniature pigs, and full‐thickness wounds were generated on their dorsum. These wounds were either allowed to heal by secondary intention alone (control) or treated with a single or multiple treatments of a porcine autologous BLCC. Results indicated a single treatment with porcine BLCC resulted in statistically significant wound healing at day 17, while four treatments resulted in statistically significant healing on days 10, 13, and 17 compared to control. Statistically accelerated wound closure was driven by re‐epithelialisation rather than contraction or granulation. This porcine diabetic model and the use of a porcine BLCC allowed evaluation of healing responses in vivo without the complications typically seen with either xenogenic responses of human/animal systems or the use of immune compromised animals, expanding the knowledge base around how BLCC may impact chronic wounds. |
format | Online Article Text |
id | pubmed-9885468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-98854682023-02-01 Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model Avery, Justin T. Qiao, Jizeng Medeiros, Erika Bollenbach, Thomas J. Kimmerling, Kelly A. Mowry, Katie C. Int Wound J Original Articles Tissue‐engineered skin constructs, including bi‐layered living cellular constructs (BLCC) used in the treatment of chronic wounds, are structurally/functionally complex. While some work has been performed to understand their mechanisms, the totality of how BLCC may function in wound healing remains unknown. To this end, we have developed a delayed wound healing model to test BLCC cellular and molecular mechanisms of action. Diabetes was chemically‐induced using alloxan in Yucatan miniature pigs, and full‐thickness wounds were generated on their dorsum. These wounds were either allowed to heal by secondary intention alone (control) or treated with a single or multiple treatments of a porcine autologous BLCC. Results indicated a single treatment with porcine BLCC resulted in statistically significant wound healing at day 17, while four treatments resulted in statistically significant healing on days 10, 13, and 17 compared to control. Statistically accelerated wound closure was driven by re‐epithelialisation rather than contraction or granulation. This porcine diabetic model and the use of a porcine BLCC allowed evaluation of healing responses in vivo without the complications typically seen with either xenogenic responses of human/animal systems or the use of immune compromised animals, expanding the knowledge base around how BLCC may impact chronic wounds. Blackwell Publishing Ltd 2022-08-02 /pmc/articles/PMC9885468/ /pubmed/35918057 http://dx.doi.org/10.1111/iwj.13889 Text en © 2022 Organogenesis. International Wound Journal published by Medicalhelplines.com Inc (3M) and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Avery, Justin T. Qiao, Jizeng Medeiros, Erika Bollenbach, Thomas J. Kimmerling, Kelly A. Mowry, Katie C. Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
title |
Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
title_full |
Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
title_fullStr |
Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
title_full_unstemmed |
Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
title_short |
Bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
title_sort | bi‐layered living cellular construct resulted in greater healing in an alloxan‐induced diabetic porcine model |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885468/ https://www.ncbi.nlm.nih.gov/pubmed/35918057 http://dx.doi.org/10.1111/iwj.13889 |
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