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Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation

Liver synthetic and metabolic function can only be optimised by the growth of cells within a supportive liver matrix. This can be achieved by the utilisation of decellularised human liver tissue. Here we demonstrate complete decellularization of whole human liver and lobes to form an extracellular m...

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Autores principales: Mazza, Giuseppe, Rombouts, Krista, Rennie Hall, Andrew, Urbani, Luca, Vinh Luong, Tu, Al-Akkad, Walid, Longato, Lisa, Brown, David, Maghsoudlou, Panagiotis, Dhillon, Amar P., Fuller, Barry, Davidson, Brian, Moore, Kevin, Dhar, Dipok, De Coppi, Paolo, Malago, Massimo, Pinzani, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528226/
https://www.ncbi.nlm.nih.gov/pubmed/26248878
http://dx.doi.org/10.1038/srep13079
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author Mazza, Giuseppe
Rombouts, Krista
Rennie Hall, Andrew
Urbani, Luca
Vinh Luong, Tu
Al-Akkad, Walid
Longato, Lisa
Brown, David
Maghsoudlou, Panagiotis
Dhillon, Amar P.
Fuller, Barry
Davidson, Brian
Moore, Kevin
Dhar, Dipok
De Coppi, Paolo
Malago, Massimo
Pinzani, Massimo
author_facet Mazza, Giuseppe
Rombouts, Krista
Rennie Hall, Andrew
Urbani, Luca
Vinh Luong, Tu
Al-Akkad, Walid
Longato, Lisa
Brown, David
Maghsoudlou, Panagiotis
Dhillon, Amar P.
Fuller, Barry
Davidson, Brian
Moore, Kevin
Dhar, Dipok
De Coppi, Paolo
Malago, Massimo
Pinzani, Massimo
author_sort Mazza, Giuseppe
collection PubMed
description Liver synthetic and metabolic function can only be optimised by the growth of cells within a supportive liver matrix. This can be achieved by the utilisation of decellularised human liver tissue. Here we demonstrate complete decellularization of whole human liver and lobes to form an extracellular matrix scaffold with a preserved architecture. Decellularized human liver cubic scaffolds were repopulated for up to 21 days using human cell lines hepatic stellate cells (LX2), hepatocellular carcinoma (Sk-Hep-1) and hepatoblastoma (HepG2), with excellent viability, motility and proliferation and remodelling of the extracellular matrix. Biocompatibility was demonstrated by either omental or subcutaneous xenotransplantation of liver scaffold cubes (5 × 5 × 5 mm) into immune competent mice resulting in absent foreign body responses. We demonstrate decellularization of human liver and repopulation with derived human liver cells. This is a key advance in bioartificial liver development.
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spelling pubmed-45282262015-08-07 Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation Mazza, Giuseppe Rombouts, Krista Rennie Hall, Andrew Urbani, Luca Vinh Luong, Tu Al-Akkad, Walid Longato, Lisa Brown, David Maghsoudlou, Panagiotis Dhillon, Amar P. Fuller, Barry Davidson, Brian Moore, Kevin Dhar, Dipok De Coppi, Paolo Malago, Massimo Pinzani, Massimo Sci Rep Article Liver synthetic and metabolic function can only be optimised by the growth of cells within a supportive liver matrix. This can be achieved by the utilisation of decellularised human liver tissue. Here we demonstrate complete decellularization of whole human liver and lobes to form an extracellular matrix scaffold with a preserved architecture. Decellularized human liver cubic scaffolds were repopulated for up to 21 days using human cell lines hepatic stellate cells (LX2), hepatocellular carcinoma (Sk-Hep-1) and hepatoblastoma (HepG2), with excellent viability, motility and proliferation and remodelling of the extracellular matrix. Biocompatibility was demonstrated by either omental or subcutaneous xenotransplantation of liver scaffold cubes (5 × 5 × 5 mm) into immune competent mice resulting in absent foreign body responses. We demonstrate decellularization of human liver and repopulation with derived human liver cells. This is a key advance in bioartificial liver development. Nature Publishing Group 2015-08-07 /pmc/articles/PMC4528226/ /pubmed/26248878 http://dx.doi.org/10.1038/srep13079 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Mazza, Giuseppe
Rombouts, Krista
Rennie Hall, Andrew
Urbani, Luca
Vinh Luong, Tu
Al-Akkad, Walid
Longato, Lisa
Brown, David
Maghsoudlou, Panagiotis
Dhillon, Amar P.
Fuller, Barry
Davidson, Brian
Moore, Kevin
Dhar, Dipok
De Coppi, Paolo
Malago, Massimo
Pinzani, Massimo
Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation
title Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation
title_full Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation
title_fullStr Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation
title_full_unstemmed Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation
title_short Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation
title_sort decellularized human liver as a natural 3d-scaffold for liver bioengineering and transplantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528226/
https://www.ncbi.nlm.nih.gov/pubmed/26248878
http://dx.doi.org/10.1038/srep13079
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