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A Chemically Defined Hydrogel for Human Liver Organoid Culture
End-stage liver diseases are an increasing health burden, and liver transplantations are currently the only curative treatment option. Due to a lack of donor livers, alternative treatments are urgently needed. Human liver organoids are very promising for regenerative medicine; however, organoids are...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611838/ https://www.ncbi.nlm.nih.gov/pubmed/34658689 http://dx.doi.org/10.1002/adfm.202000893 |
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author | Ye, Shicheng Boeter, Jochem W.B. Mihajlovic, Marko van Steenbeek, Frank G. van Wolferen, Monique E. Oosterhoff, Loes A. Marsee, Ary Caiazzo, Massimiliano van der Laan, Luc J.W. Penning, Louis C. Vermonden, Tina Spee, Bart Schneeberger, Kerstin |
author_facet | Ye, Shicheng Boeter, Jochem W.B. Mihajlovic, Marko van Steenbeek, Frank G. van Wolferen, Monique E. Oosterhoff, Loes A. Marsee, Ary Caiazzo, Massimiliano van der Laan, Luc J.W. Penning, Louis C. Vermonden, Tina Spee, Bart Schneeberger, Kerstin |
author_sort | Ye, Shicheng |
collection | PubMed |
description | End-stage liver diseases are an increasing health burden, and liver transplantations are currently the only curative treatment option. Due to a lack of donor livers, alternative treatments are urgently needed. Human liver organoids are very promising for regenerative medicine; however, organoids are currently cultured in Matrigel, which is extracted from the extracellular matrix of the Engelbreth-Holm-Swarm mouse sarcoma. Matrigel is poorly defined, suffers from high batch-to-batch variability and is of xenogeneic origin, which limits the clinical application of organoids. Here, a novel hydrogel based on polyisocyanopeptides (PIC) and laminin-111 is described for human liver organoid cultures. PIC is a synthetic polymer that can form a hydrogel with thermosensitive properties, making it easy to handle and very attractive for clinical applications. Organoids in an optimized PIC hydrogel proliferate at rates comparable to those observed with Matrigel; proliferation rates are stiffness-dependent, with lower stiffnesses being optimal for organoid proliferation. Moreover, organoids can be efficiently differentiated toward a hepatocyte-like phenotype with key liver functions. This proliferation and differentiation potential maintain over at least 14 passages. The results indicate that PIC is very promising for human liver organoid culture and has the potential to be used in a variety of clinical applications including cell therapy and tissue engineering. |
format | Online Article Text |
id | pubmed-7611838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76118382021-10-14 A Chemically Defined Hydrogel for Human Liver Organoid Culture Ye, Shicheng Boeter, Jochem W.B. Mihajlovic, Marko van Steenbeek, Frank G. van Wolferen, Monique E. Oosterhoff, Loes A. Marsee, Ary Caiazzo, Massimiliano van der Laan, Luc J.W. Penning, Louis C. Vermonden, Tina Spee, Bart Schneeberger, Kerstin Adv Funct Mater Article End-stage liver diseases are an increasing health burden, and liver transplantations are currently the only curative treatment option. Due to a lack of donor livers, alternative treatments are urgently needed. Human liver organoids are very promising for regenerative medicine; however, organoids are currently cultured in Matrigel, which is extracted from the extracellular matrix of the Engelbreth-Holm-Swarm mouse sarcoma. Matrigel is poorly defined, suffers from high batch-to-batch variability and is of xenogeneic origin, which limits the clinical application of organoids. Here, a novel hydrogel based on polyisocyanopeptides (PIC) and laminin-111 is described for human liver organoid cultures. PIC is a synthetic polymer that can form a hydrogel with thermosensitive properties, making it easy to handle and very attractive for clinical applications. Organoids in an optimized PIC hydrogel proliferate at rates comparable to those observed with Matrigel; proliferation rates are stiffness-dependent, with lower stiffnesses being optimal for organoid proliferation. Moreover, organoids can be efficiently differentiated toward a hepatocyte-like phenotype with key liver functions. This proliferation and differentiation potential maintain over at least 14 passages. The results indicate that PIC is very promising for human liver organoid culture and has the potential to be used in a variety of clinical applications including cell therapy and tissue engineering. 2020-06-08 /pmc/articles/PMC7611838/ /pubmed/34658689 http://dx.doi.org/10.1002/adfm.202000893 Text en This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Article Ye, Shicheng Boeter, Jochem W.B. Mihajlovic, Marko van Steenbeek, Frank G. van Wolferen, Monique E. Oosterhoff, Loes A. Marsee, Ary Caiazzo, Massimiliano van der Laan, Luc J.W. Penning, Louis C. Vermonden, Tina Spee, Bart Schneeberger, Kerstin A Chemically Defined Hydrogel for Human Liver Organoid Culture |
title | A Chemically Defined Hydrogel for Human Liver Organoid Culture |
title_full | A Chemically Defined Hydrogel for Human Liver Organoid Culture |
title_fullStr | A Chemically Defined Hydrogel for Human Liver Organoid Culture |
title_full_unstemmed | A Chemically Defined Hydrogel for Human Liver Organoid Culture |
title_short | A Chemically Defined Hydrogel for Human Liver Organoid Culture |
title_sort | chemically defined hydrogel for human liver organoid culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7611838/ https://www.ncbi.nlm.nih.gov/pubmed/34658689 http://dx.doi.org/10.1002/adfm.202000893 |
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