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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...

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Autores principales: Avery, Justin T., Qiao, Jizeng, Medeiros, Erika, Bollenbach, Thomas J., Kimmerling, Kelly A., Mowry, Katie C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
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.
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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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