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Stem cell-derived polarized hepatocytes
Human stem cell-derived hepatocyte-like cells (HLCs) offer an attractive platform to study liver biology. Despite their numerous advantages, HLCs lack critical in vivo characteristics, including cell polarity. Here, we report a stem cell differentiation protocol that uses transwell filters to genera...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125181/ https://www.ncbi.nlm.nih.gov/pubmed/32245952 http://dx.doi.org/10.1038/s41467-020-15337-2 |
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author | Dao Thi, Viet Loan Wu, Xianfang Belote, Rachel L. Andreo, Ursula Takacs, Constantin N. Fernandez, Joseph P. Vale-Silva, Luis Andre Prallet, Sarah Decker, Charlotte C. Fu, Rebecca M. Qu, Bingqian Uryu, Kunihiro Molina, Henrik Saeed, Mohsan Steinmann, Eike Urban, Stephan Singaraja, Roshni R. Schneider, William M. Simon, Sanford M. Rice, Charles M. |
author_facet | Dao Thi, Viet Loan Wu, Xianfang Belote, Rachel L. Andreo, Ursula Takacs, Constantin N. Fernandez, Joseph P. Vale-Silva, Luis Andre Prallet, Sarah Decker, Charlotte C. Fu, Rebecca M. Qu, Bingqian Uryu, Kunihiro Molina, Henrik Saeed, Mohsan Steinmann, Eike Urban, Stephan Singaraja, Roshni R. Schneider, William M. Simon, Sanford M. Rice, Charles M. |
author_sort | Dao Thi, Viet Loan |
collection | PubMed |
description | Human stem cell-derived hepatocyte-like cells (HLCs) offer an attractive platform to study liver biology. Despite their numerous advantages, HLCs lack critical in vivo characteristics, including cell polarity. Here, we report a stem cell differentiation protocol that uses transwell filters to generate columnar polarized HLCs with clearly defined basolateral and apical membranes separated by tight junctions. We show that polarized HLCs secrete cargo directionally: Albumin, urea, and lipoproteins are secreted basolaterally, whereas bile acids are secreted apically. Further, we show that enterically transmitted hepatitis E virus (HEV) progeny particles are secreted basolaterally as quasi-enveloped particles and apically as naked virions, recapitulating essential steps of the natural infectious cycle in vivo. We also provide proof-of-concept that polarized HLCs can be used for pharmacokinetic and drug-drug interaction studies. This novel system provides a powerful tool to study hepatocyte biology, disease mechanisms, genetic variation, and drug metabolism in a more physiologically relevant setting. |
format | Online Article Text |
id | pubmed-7125181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71251812020-04-06 Stem cell-derived polarized hepatocytes Dao Thi, Viet Loan Wu, Xianfang Belote, Rachel L. Andreo, Ursula Takacs, Constantin N. Fernandez, Joseph P. Vale-Silva, Luis Andre Prallet, Sarah Decker, Charlotte C. Fu, Rebecca M. Qu, Bingqian Uryu, Kunihiro Molina, Henrik Saeed, Mohsan Steinmann, Eike Urban, Stephan Singaraja, Roshni R. Schneider, William M. Simon, Sanford M. Rice, Charles M. Nat Commun Article Human stem cell-derived hepatocyte-like cells (HLCs) offer an attractive platform to study liver biology. Despite their numerous advantages, HLCs lack critical in vivo characteristics, including cell polarity. Here, we report a stem cell differentiation protocol that uses transwell filters to generate columnar polarized HLCs with clearly defined basolateral and apical membranes separated by tight junctions. We show that polarized HLCs secrete cargo directionally: Albumin, urea, and lipoproteins are secreted basolaterally, whereas bile acids are secreted apically. Further, we show that enterically transmitted hepatitis E virus (HEV) progeny particles are secreted basolaterally as quasi-enveloped particles and apically as naked virions, recapitulating essential steps of the natural infectious cycle in vivo. We also provide proof-of-concept that polarized HLCs can be used for pharmacokinetic and drug-drug interaction studies. This novel system provides a powerful tool to study hepatocyte biology, disease mechanisms, genetic variation, and drug metabolism in a more physiologically relevant setting. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125181/ /pubmed/32245952 http://dx.doi.org/10.1038/s41467-020-15337-2 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dao Thi, Viet Loan Wu, Xianfang Belote, Rachel L. Andreo, Ursula Takacs, Constantin N. Fernandez, Joseph P. Vale-Silva, Luis Andre Prallet, Sarah Decker, Charlotte C. Fu, Rebecca M. Qu, Bingqian Uryu, Kunihiro Molina, Henrik Saeed, Mohsan Steinmann, Eike Urban, Stephan Singaraja, Roshni R. Schneider, William M. Simon, Sanford M. Rice, Charles M. Stem cell-derived polarized hepatocytes |
title | Stem cell-derived polarized hepatocytes |
title_full | Stem cell-derived polarized hepatocytes |
title_fullStr | Stem cell-derived polarized hepatocytes |
title_full_unstemmed | Stem cell-derived polarized hepatocytes |
title_short | Stem cell-derived polarized hepatocytes |
title_sort | stem cell-derived polarized hepatocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125181/ https://www.ncbi.nlm.nih.gov/pubmed/32245952 http://dx.doi.org/10.1038/s41467-020-15337-2 |
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