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From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation
Although the underlying cause may vary across countries and demographic groups, liver disease is a major cause of morbidity and mortality globally. Orthotopic liver transplantation is the only definitive treatment for liver failure but is limited by the lack of donor livers. The development of drugs...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Medical Publishers, Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718640/ https://www.ncbi.nlm.nih.gov/pubmed/36044927 http://dx.doi.org/10.1055/a-1934-5404 |
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author | Motomura, Takashi Faccioli, Lanuza A.P. Diaz-Aragon, Ricardo Kocas-Kilicarslan, Zehra N. Haep, Nils Florentino, Rodrigo M. Amirneni, Sriram Cetin, Zeliha Peri, Bhaavna S. Morita, Kazutoyo Ostrowska, Alina Takeishi, Kazuki Soto-Gutierrez, Alejandro Tafaleng, Edgar N. |
author_facet | Motomura, Takashi Faccioli, Lanuza A.P. Diaz-Aragon, Ricardo Kocas-Kilicarslan, Zehra N. Haep, Nils Florentino, Rodrigo M. Amirneni, Sriram Cetin, Zeliha Peri, Bhaavna S. Morita, Kazutoyo Ostrowska, Alina Takeishi, Kazuki Soto-Gutierrez, Alejandro Tafaleng, Edgar N. |
author_sort | Motomura, Takashi |
collection | PubMed |
description | Although the underlying cause may vary across countries and demographic groups, liver disease is a major cause of morbidity and mortality globally. Orthotopic liver transplantation is the only definitive treatment for liver failure but is limited by the lack of donor livers. The development of drugs that prevent the progression of liver disease and the generation of alternative liver constructs for transplantation could help alleviate the burden of liver disease. Bioengineered livers containing human induced pluripotent stem cell (iPSC)–derived liver cells are being utilized to study liver disease and to identify and test potential therapeutics. Moreover, bioengineered livers containing pig hepatocytes and endothelial cells have been shown to function and survive after transplantation into pig models of liver failure, providing preclinical evidence toward future clinical applications. Finally, bioengineered livers containing human iPSC-derived liver cells have been shown to function and survive after transplantation in rodents but require considerable optimization and testing prior to clinical use. In conclusion, bioengineered livers have emerged as a suitable tool for modeling liver diseases and as a promising alternative graft for clinical transplantation. The integration of novel technologies and techniques for the assembly and analysis of bioengineered livers will undoubtedly expand future applications in basic research and clinical transplantation. |
format | Online Article Text |
id | pubmed-9718640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Thieme Medical Publishers, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97186402022-12-03 From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation Motomura, Takashi Faccioli, Lanuza A.P. Diaz-Aragon, Ricardo Kocas-Kilicarslan, Zehra N. Haep, Nils Florentino, Rodrigo M. Amirneni, Sriram Cetin, Zeliha Peri, Bhaavna S. Morita, Kazutoyo Ostrowska, Alina Takeishi, Kazuki Soto-Gutierrez, Alejandro Tafaleng, Edgar N. Semin Liver Dis Although the underlying cause may vary across countries and demographic groups, liver disease is a major cause of morbidity and mortality globally. Orthotopic liver transplantation is the only definitive treatment for liver failure but is limited by the lack of donor livers. The development of drugs that prevent the progression of liver disease and the generation of alternative liver constructs for transplantation could help alleviate the burden of liver disease. Bioengineered livers containing human induced pluripotent stem cell (iPSC)–derived liver cells are being utilized to study liver disease and to identify and test potential therapeutics. Moreover, bioengineered livers containing pig hepatocytes and endothelial cells have been shown to function and survive after transplantation into pig models of liver failure, providing preclinical evidence toward future clinical applications. Finally, bioengineered livers containing human iPSC-derived liver cells have been shown to function and survive after transplantation in rodents but require considerable optimization and testing prior to clinical use. In conclusion, bioengineered livers have emerged as a suitable tool for modeling liver diseases and as a promising alternative graft for clinical transplantation. The integration of novel technologies and techniques for the assembly and analysis of bioengineered livers will undoubtedly expand future applications in basic research and clinical transplantation. Thieme Medical Publishers, Inc. 2022-10-19 /pmc/articles/PMC9718640/ /pubmed/36044927 http://dx.doi.org/10.1055/a-1934-5404 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Motomura, Takashi Faccioli, Lanuza A.P. Diaz-Aragon, Ricardo Kocas-Kilicarslan, Zehra N. Haep, Nils Florentino, Rodrigo M. Amirneni, Sriram Cetin, Zeliha Peri, Bhaavna S. Morita, Kazutoyo Ostrowska, Alina Takeishi, Kazuki Soto-Gutierrez, Alejandro Tafaleng, Edgar N. From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation |
title | From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation |
title_full | From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation |
title_fullStr | From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation |
title_full_unstemmed | From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation |
title_short | From a Single Cell to a Whole Human Liver: Disease Modeling and Transplantation |
title_sort | from a single cell to a whole human liver: disease modeling and transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718640/ https://www.ncbi.nlm.nih.gov/pubmed/36044927 http://dx.doi.org/10.1055/a-1934-5404 |
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