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In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions
Hepatocyte-like cells derived from human pluripotent stem cells (hPSC-HLCs) offer an alternative to primary hepatocytes commonly used for drug screenings and toxicological tests. However, these cells do not have hepatic functions comparable to those of hepatocytes in vivo due to insufficient hepatic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956733/ https://www.ncbi.nlm.nih.gov/pubmed/35338220 http://dx.doi.org/10.1038/s41598-022-09119-7 |
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author | Imamura, Satoshi Yoshimoto, Koki Terada, Shiho Takamuro, Kaho Kamei, Ken-ichiro |
author_facet | Imamura, Satoshi Yoshimoto, Koki Terada, Shiho Takamuro, Kaho Kamei, Ken-ichiro |
author_sort | Imamura, Satoshi |
collection | PubMed |
description | Hepatocyte-like cells derived from human pluripotent stem cells (hPSC-HLCs) offer an alternative to primary hepatocytes commonly used for drug screenings and toxicological tests. However, these cells do not have hepatic functions comparable to those of hepatocytes in vivo due to insufficient hepatic differentiation. Here we showed that the hepatic functions of hPSC-HLCs were facilitated by applying physiological liver temperatures during hepatic differentiation. We identified the optimal temperature by treating HLCs derived from H9 human embryonic stem cells (hESC-HLCs) at 39 °C; the 42 °C treatment caused significantly greater cell death than the 39 °C treatment. We confirmed the improvement of hepatic functions, such as albumin secretion, cytochrome P450 3A activity, and collagen production, without severe cell damage. In combination with existing hepatic differentiation protocols, the method proposed here may further improve hepatic functions for hPSCs and lead to the realization of drug discovery efforts and drug toxicological tests. |
format | Online Article Text |
id | pubmed-8956733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89567332022-03-30 In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions Imamura, Satoshi Yoshimoto, Koki Terada, Shiho Takamuro, Kaho Kamei, Ken-ichiro Sci Rep Article Hepatocyte-like cells derived from human pluripotent stem cells (hPSC-HLCs) offer an alternative to primary hepatocytes commonly used for drug screenings and toxicological tests. However, these cells do not have hepatic functions comparable to those of hepatocytes in vivo due to insufficient hepatic differentiation. Here we showed that the hepatic functions of hPSC-HLCs were facilitated by applying physiological liver temperatures during hepatic differentiation. We identified the optimal temperature by treating HLCs derived from H9 human embryonic stem cells (hESC-HLCs) at 39 °C; the 42 °C treatment caused significantly greater cell death than the 39 °C treatment. We confirmed the improvement of hepatic functions, such as albumin secretion, cytochrome P450 3A activity, and collagen production, without severe cell damage. In combination with existing hepatic differentiation protocols, the method proposed here may further improve hepatic functions for hPSCs and lead to the realization of drug discovery efforts and drug toxicological tests. Nature Publishing Group UK 2022-03-25 /pmc/articles/PMC8956733/ /pubmed/35338220 http://dx.doi.org/10.1038/s41598-022-09119-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Imamura, Satoshi Yoshimoto, Koki Terada, Shiho Takamuro, Kaho Kamei, Ken-ichiro In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions |
title | In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions |
title_full | In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions |
title_fullStr | In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions |
title_full_unstemmed | In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions |
title_short | In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions |
title_sort | in vitro culture at 39 °c during hepatic maturation of human es cells facilitates hepatocyte-like cell functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956733/ https://www.ncbi.nlm.nih.gov/pubmed/35338220 http://dx.doi.org/10.1038/s41598-022-09119-7 |
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