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Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications
To expand the application of perfusion decellularization beyond isolated single organs, we used the native vasculature of adult and neonatal rats to systemically decellularize the organs of a whole animal in situ. Acellular scaffolds were generated from kidney, liver, lower limb, heart‐lung system,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239446/ https://www.ncbi.nlm.nih.gov/pubmed/34184419 http://dx.doi.org/10.14814/phy2.14817 |
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author | Taylor, Doris A. Kren, Stefan M. Rhett, Katrina Robertson, Matthew J. Morrissey, Jacquelynn Rodriguez, Osman E. Virk, Hassan Chacon‐Alberty, Lourdes Curty da Costa, Ernesto Mesquita, Fernanda C. P. Sampaio, Luiz C. Hochman‐Mendez, Camila |
author_facet | Taylor, Doris A. Kren, Stefan M. Rhett, Katrina Robertson, Matthew J. Morrissey, Jacquelynn Rodriguez, Osman E. Virk, Hassan Chacon‐Alberty, Lourdes Curty da Costa, Ernesto Mesquita, Fernanda C. P. Sampaio, Luiz C. Hochman‐Mendez, Camila |
author_sort | Taylor, Doris A. |
collection | PubMed |
description | To expand the application of perfusion decellularization beyond isolated single organs, we used the native vasculature of adult and neonatal rats to systemically decellularize the organs of a whole animal in situ. Acellular scaffolds were generated from kidney, liver, lower limb, heart‐lung system, and a whole animal body, demonstrating that perfusion decellularization technology is applicable to any perfusable tissue, independent of age. Biochemical and histological analyses demonstrated that organs and organ systems (heart‐lung pair and lower limb) were successfully decellularized, retaining their extracellular matrix (ECM) structure and organ‐specific composition, as evidenced by differences in organ‐specific scaffold stiffness. Altogether, we demonstrated that organs, organ systems and whole animal bodies can be perfusion decellularized while retaining ECM components and biomechanics. |
format | Online Article Text |
id | pubmed-8239446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82394462021-07-02 Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications Taylor, Doris A. Kren, Stefan M. Rhett, Katrina Robertson, Matthew J. Morrissey, Jacquelynn Rodriguez, Osman E. Virk, Hassan Chacon‐Alberty, Lourdes Curty da Costa, Ernesto Mesquita, Fernanda C. P. Sampaio, Luiz C. Hochman‐Mendez, Camila Physiol Rep Original Articles To expand the application of perfusion decellularization beyond isolated single organs, we used the native vasculature of adult and neonatal rats to systemically decellularize the organs of a whole animal in situ. Acellular scaffolds were generated from kidney, liver, lower limb, heart‐lung system, and a whole animal body, demonstrating that perfusion decellularization technology is applicable to any perfusable tissue, independent of age. Biochemical and histological analyses demonstrated that organs and organ systems (heart‐lung pair and lower limb) were successfully decellularized, retaining their extracellular matrix (ECM) structure and organ‐specific composition, as evidenced by differences in organ‐specific scaffold stiffness. Altogether, we demonstrated that organs, organ systems and whole animal bodies can be perfusion decellularized while retaining ECM components and biomechanics. John Wiley and Sons Inc. 2021-06-29 /pmc/articles/PMC8239446/ /pubmed/34184419 http://dx.doi.org/10.14814/phy2.14817 Text en © 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society 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 | Original Articles Taylor, Doris A. Kren, Stefan M. Rhett, Katrina Robertson, Matthew J. Morrissey, Jacquelynn Rodriguez, Osman E. Virk, Hassan Chacon‐Alberty, Lourdes Curty da Costa, Ernesto Mesquita, Fernanda C. P. Sampaio, Luiz C. Hochman‐Mendez, Camila Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
title | Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
title_full | Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
title_fullStr | Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
title_full_unstemmed | Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
title_short | Characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
title_sort | characterization of perfusion decellularized whole animal body, isolated organs, and multi‐organ systems for tissue engineering applications |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239446/ https://www.ncbi.nlm.nih.gov/pubmed/34184419 http://dx.doi.org/10.14814/phy2.14817 |
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