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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,...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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