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In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells

In this study we used differentiated adult human upcyte(®) cells for the in vitro generation of liver organoids. Upcyte(®) cells are genetically engineered cell strains derived from primary human cells by lenti-viral transduction of genes or gene combinations inducing transient proliferation capacit...

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Autores principales: Ramachandran, Sarada Devi, Schirmer, Katharina, Münst, Bernhard, Heinz, Stefan, Ghafoory, Shahrouz, Wölfl, Stefan, Simon-Keller, Katja, Marx, Alexander, Øie, Cristina Ionica, Ebert, Matthias P., Walles, Heike, Braspenning, Joris, Breitkopf-Heinlein, Katja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619350/
https://www.ncbi.nlm.nih.gov/pubmed/26488607
http://dx.doi.org/10.1371/journal.pone.0139345
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author Ramachandran, Sarada Devi
Schirmer, Katharina
Münst, Bernhard
Heinz, Stefan
Ghafoory, Shahrouz
Wölfl, Stefan
Simon-Keller, Katja
Marx, Alexander
Øie, Cristina Ionica
Ebert, Matthias P.
Walles, Heike
Braspenning, Joris
Breitkopf-Heinlein, Katja
author_facet Ramachandran, Sarada Devi
Schirmer, Katharina
Münst, Bernhard
Heinz, Stefan
Ghafoory, Shahrouz
Wölfl, Stefan
Simon-Keller, Katja
Marx, Alexander
Øie, Cristina Ionica
Ebert, Matthias P.
Walles, Heike
Braspenning, Joris
Breitkopf-Heinlein, Katja
author_sort Ramachandran, Sarada Devi
collection PubMed
description In this study we used differentiated adult human upcyte(®) cells for the in vitro generation of liver organoids. Upcyte(®) cells are genetically engineered cell strains derived from primary human cells by lenti-viral transduction of genes or gene combinations inducing transient proliferation capacity (upcyte(®) process). Proliferating upcyte(®) cells undergo a finite number of cell divisions, i.e., 20 to 40 population doublings, but upon withdrawal of proliferation stimulating factors, they regain most of the cell specific characteristics of primary cells. When a defined mixture of differentiated human upcyte(®) cells (hepatocytes, liver sinusoidal endothelial cells (LSECs) and mesenchymal stem cells (MSCs)) was cultured in vitro on a thick layer of Matrigel™, they self-organized to form liver organoid-like structures within 24 hours. When further cultured for 10 days in a bioreactor, these liver organoids show typical functional characteristics of liver parenchyma including activity of cytochromes P450, CYP3A4, CYP2B6 and CYP2C9 as well as mRNA expression of several marker genes and other enzymes. In summary, we hereby describe that 3D functional hepatic structures composed of primary human cell strains can be generated in vitro. They can be cultured for a prolonged period of time and are potentially useful ex vivo models to study liver functions.
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spelling pubmed-46193502015-10-29 In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells Ramachandran, Sarada Devi Schirmer, Katharina Münst, Bernhard Heinz, Stefan Ghafoory, Shahrouz Wölfl, Stefan Simon-Keller, Katja Marx, Alexander Øie, Cristina Ionica Ebert, Matthias P. Walles, Heike Braspenning, Joris Breitkopf-Heinlein, Katja PLoS One Research Article In this study we used differentiated adult human upcyte(®) cells for the in vitro generation of liver organoids. Upcyte(®) cells are genetically engineered cell strains derived from primary human cells by lenti-viral transduction of genes or gene combinations inducing transient proliferation capacity (upcyte(®) process). Proliferating upcyte(®) cells undergo a finite number of cell divisions, i.e., 20 to 40 population doublings, but upon withdrawal of proliferation stimulating factors, they regain most of the cell specific characteristics of primary cells. When a defined mixture of differentiated human upcyte(®) cells (hepatocytes, liver sinusoidal endothelial cells (LSECs) and mesenchymal stem cells (MSCs)) was cultured in vitro on a thick layer of Matrigel™, they self-organized to form liver organoid-like structures within 24 hours. When further cultured for 10 days in a bioreactor, these liver organoids show typical functional characteristics of liver parenchyma including activity of cytochromes P450, CYP3A4, CYP2B6 and CYP2C9 as well as mRNA expression of several marker genes and other enzymes. In summary, we hereby describe that 3D functional hepatic structures composed of primary human cell strains can be generated in vitro. They can be cultured for a prolonged period of time and are potentially useful ex vivo models to study liver functions. Public Library of Science 2015-10-21 /pmc/articles/PMC4619350/ /pubmed/26488607 http://dx.doi.org/10.1371/journal.pone.0139345 Text en © 2015 Ramachandran et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ramachandran, Sarada Devi
Schirmer, Katharina
Münst, Bernhard
Heinz, Stefan
Ghafoory, Shahrouz
Wölfl, Stefan
Simon-Keller, Katja
Marx, Alexander
Øie, Cristina Ionica
Ebert, Matthias P.
Walles, Heike
Braspenning, Joris
Breitkopf-Heinlein, Katja
In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells
title In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells
title_full In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells
title_fullStr In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells
title_full_unstemmed In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells
title_short In Vitro Generation of Functional Liver Organoid-Like Structures Using Adult Human Cells
title_sort in vitro generation of functional liver organoid-like structures using adult human cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619350/
https://www.ncbi.nlm.nih.gov/pubmed/26488607
http://dx.doi.org/10.1371/journal.pone.0139345
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