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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4528226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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