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High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds
In Europe alone, each year 5500 people require a life‐saving liver transplantation, but 18% die before receiving one due to the shortage of donor organs. Whole organ engineering, utilizing decellularized liver scaffolds repopulated with autologous cells, is an attractive alternative to increase the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549510/ https://www.ncbi.nlm.nih.gov/pubmed/36017767 http://dx.doi.org/10.1111/jcmm.17510 |
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author | Krüger, Melanie Samsom, Roos‐Anne Oosterhoff, Loes A. van Wolferen, Monique E. Kooistra, Hans S. Geijsen, Niels Penning, Louis C. Kock, Linda M. Sainz‐Arnal, Pilar Baptista, Pedro M. Spee, Bart |
author_facet | Krüger, Melanie Samsom, Roos‐Anne Oosterhoff, Loes A. van Wolferen, Monique E. Kooistra, Hans S. Geijsen, Niels Penning, Louis C. Kock, Linda M. Sainz‐Arnal, Pilar Baptista, Pedro M. Spee, Bart |
author_sort | Krüger, Melanie |
collection | PubMed |
description | In Europe alone, each year 5500 people require a life‐saving liver transplantation, but 18% die before receiving one due to the shortage of donor organs. Whole organ engineering, utilizing decellularized liver scaffolds repopulated with autologous cells, is an attractive alternative to increase the pool of available organs for transplantation. The development of this technology is hampered by a lack of a suitable large‐animal model representative of the human physiology and a reliable and continuous cell source. We have generated porcine intrahepatic cholangiocyte organoids from adult stem cells and demonstrate that these cultures remained stable over multiple passages whilst retaining the ability to differentiate into hepatocyte‐ and cholangiocyte‐like cells. Recellularization onto porcine scaffolds was efficient and the organoids homogeneously differentiated, even showing polarization. Our porcine intrahepatic cholangiocyte system, combined with porcine liver scaffold paves the way for developing whole liver engineering in a relevant large‐animal model. |
format | Online Article Text |
id | pubmed-9549510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95495102022-10-14 High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds Krüger, Melanie Samsom, Roos‐Anne Oosterhoff, Loes A. van Wolferen, Monique E. Kooistra, Hans S. Geijsen, Niels Penning, Louis C. Kock, Linda M. Sainz‐Arnal, Pilar Baptista, Pedro M. Spee, Bart J Cell Mol Med Original Articles In Europe alone, each year 5500 people require a life‐saving liver transplantation, but 18% die before receiving one due to the shortage of donor organs. Whole organ engineering, utilizing decellularized liver scaffolds repopulated with autologous cells, is an attractive alternative to increase the pool of available organs for transplantation. The development of this technology is hampered by a lack of a suitable large‐animal model representative of the human physiology and a reliable and continuous cell source. We have generated porcine intrahepatic cholangiocyte organoids from adult stem cells and demonstrate that these cultures remained stable over multiple passages whilst retaining the ability to differentiate into hepatocyte‐ and cholangiocyte‐like cells. Recellularization onto porcine scaffolds was efficient and the organoids homogeneously differentiated, even showing polarization. Our porcine intrahepatic cholangiocyte system, combined with porcine liver scaffold paves the way for developing whole liver engineering in a relevant large‐animal model. John Wiley and Sons Inc. 2022-08-26 2022-10 /pmc/articles/PMC9549510/ /pubmed/36017767 http://dx.doi.org/10.1111/jcmm.17510 Text en © 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. 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 Krüger, Melanie Samsom, Roos‐Anne Oosterhoff, Loes A. van Wolferen, Monique E. Kooistra, Hans S. Geijsen, Niels Penning, Louis C. Kock, Linda M. Sainz‐Arnal, Pilar Baptista, Pedro M. Spee, Bart High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
title | High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
title_full | High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
title_fullStr | High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
title_full_unstemmed | High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
title_short | High level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
title_sort | high level of polarized engraftment of porcine intrahepatic cholangiocyte organoids in decellularized liver scaffolds |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549510/ https://www.ncbi.nlm.nih.gov/pubmed/36017767 http://dx.doi.org/10.1111/jcmm.17510 |
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