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Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture
Induced pluripotent stem cell derived hepatocytes (IPSC-Heps) have the potential to reduce the demand for a dwindling number of primary cells used in applications ranging from therapeutic cell infusions to in vitro toxicology studies. However, current differentiation protocols and culture methods pr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899231/ https://www.ncbi.nlm.nih.gov/pubmed/24466060 http://dx.doi.org/10.1371/journal.pone.0086372 |
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author | Gieseck III, Richard L. Hannan, Nicholas R. F. Bort, Roque Hanley, Neil A. Drake, Rosemary A. L. Cameron, Grant W. W. Wynn, Thomas A. Vallier, Ludovic |
author_facet | Gieseck III, Richard L. Hannan, Nicholas R. F. Bort, Roque Hanley, Neil A. Drake, Rosemary A. L. Cameron, Grant W. W. Wynn, Thomas A. Vallier, Ludovic |
author_sort | Gieseck III, Richard L. |
collection | PubMed |
description | Induced pluripotent stem cell derived hepatocytes (IPSC-Heps) have the potential to reduce the demand for a dwindling number of primary cells used in applications ranging from therapeutic cell infusions to in vitro toxicology studies. However, current differentiation protocols and culture methods produce cells with reduced functionality and fetal-like properties compared to adult hepatocytes. We report a culture method for the maturation of IPSC-Heps using 3-Dimensional (3D) collagen matrices compatible with high throughput screening. This culture method significantly increases functional maturation of IPSC-Heps towards an adult phenotype when compared to conventional 2D systems. Additionally, this approach spontaneously results in the presence of polarized structures necessary for drug metabolism and improves functional longevity to over 75 days. Overall, this research reveals a method to shift the phenotype of existing IPSC-Heps towards primary adult hepatocytes allowing such cells to be a more relevant replacement for the current primary standard. |
format | Online Article Text |
id | pubmed-3899231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38992312014-01-24 Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture Gieseck III, Richard L. Hannan, Nicholas R. F. Bort, Roque Hanley, Neil A. Drake, Rosemary A. L. Cameron, Grant W. W. Wynn, Thomas A. Vallier, Ludovic PLoS One Research Article Induced pluripotent stem cell derived hepatocytes (IPSC-Heps) have the potential to reduce the demand for a dwindling number of primary cells used in applications ranging from therapeutic cell infusions to in vitro toxicology studies. However, current differentiation protocols and culture methods produce cells with reduced functionality and fetal-like properties compared to adult hepatocytes. We report a culture method for the maturation of IPSC-Heps using 3-Dimensional (3D) collagen matrices compatible with high throughput screening. This culture method significantly increases functional maturation of IPSC-Heps towards an adult phenotype when compared to conventional 2D systems. Additionally, this approach spontaneously results in the presence of polarized structures necessary for drug metabolism and improves functional longevity to over 75 days. Overall, this research reveals a method to shift the phenotype of existing IPSC-Heps towards primary adult hepatocytes allowing such cells to be a more relevant replacement for the current primary standard. Public Library of Science 2014-01-22 /pmc/articles/PMC3899231/ /pubmed/24466060 http://dx.doi.org/10.1371/journal.pone.0086372 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Gieseck III, Richard L. Hannan, Nicholas R. F. Bort, Roque Hanley, Neil A. Drake, Rosemary A. L. Cameron, Grant W. W. Wynn, Thomas A. Vallier, Ludovic Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture |
title | Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture |
title_full | Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture |
title_fullStr | Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture |
title_full_unstemmed | Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture |
title_short | Maturation of Induced Pluripotent Stem Cell Derived Hepatocytes by 3D-Culture |
title_sort | maturation of induced pluripotent stem cell derived hepatocytes by 3d-culture |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899231/ https://www.ncbi.nlm.nih.gov/pubmed/24466060 http://dx.doi.org/10.1371/journal.pone.0086372 |
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