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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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