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Generation of functional ciliated cholangiocytes from human pluripotent stem cells
The derivation of mature functional cholangiocytes from human pluripotent stem cells (hPSCs) provides a model for studying the pathogenesis of cholangiopathies and for developing therapies to treat them. Current differentiation protocols are not efficient and give rise to cholangiocytes that are not...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586142/ https://www.ncbi.nlm.nih.gov/pubmed/34764255 http://dx.doi.org/10.1038/s41467-021-26764-0 |
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author | Ogawa, Mina Jiang, Jia-Xin Xia, Sunny Yang, Donghe Ding, Avrilynn Laselva, Onofrio Hernandez, Marcela Cui, Changyi Higuchi, Yuichiro Suemizu, Hiroshi Dorrell, Craig Grompe, Markus Bear, Christine E. Ogawa, Shinichiro |
author_facet | Ogawa, Mina Jiang, Jia-Xin Xia, Sunny Yang, Donghe Ding, Avrilynn Laselva, Onofrio Hernandez, Marcela Cui, Changyi Higuchi, Yuichiro Suemizu, Hiroshi Dorrell, Craig Grompe, Markus Bear, Christine E. Ogawa, Shinichiro |
author_sort | Ogawa, Mina |
collection | PubMed |
description | The derivation of mature functional cholangiocytes from human pluripotent stem cells (hPSCs) provides a model for studying the pathogenesis of cholangiopathies and for developing therapies to treat them. Current differentiation protocols are not efficient and give rise to cholangiocytes that are not fully mature, limiting their therapeutic applications. Here, we generate functional hPSC-derived cholangiocytes that display many characteristics of mature bile duct cells including high levels of cystic fibrosis transmembrane conductance regulator (CFTR) and the presence of primary cilia capable of sensing flow. With this level of maturation, these cholangiocytes are amenable for testing the efficacy of cystic fibrosis drugs and for studying the role of cilia in cholangiocyte development and function. Transplantation studies show that the mature cholangiocytes generate ductal structures in the liver of immunocompromised mice indicating that it may be possible to develop cell-based therapies to restore bile duct function in patients with biliary disease. |
format | Online Article Text |
id | pubmed-8586142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85861422021-11-15 Generation of functional ciliated cholangiocytes from human pluripotent stem cells Ogawa, Mina Jiang, Jia-Xin Xia, Sunny Yang, Donghe Ding, Avrilynn Laselva, Onofrio Hernandez, Marcela Cui, Changyi Higuchi, Yuichiro Suemizu, Hiroshi Dorrell, Craig Grompe, Markus Bear, Christine E. Ogawa, Shinichiro Nat Commun Article The derivation of mature functional cholangiocytes from human pluripotent stem cells (hPSCs) provides a model for studying the pathogenesis of cholangiopathies and for developing therapies to treat them. Current differentiation protocols are not efficient and give rise to cholangiocytes that are not fully mature, limiting their therapeutic applications. Here, we generate functional hPSC-derived cholangiocytes that display many characteristics of mature bile duct cells including high levels of cystic fibrosis transmembrane conductance regulator (CFTR) and the presence of primary cilia capable of sensing flow. With this level of maturation, these cholangiocytes are amenable for testing the efficacy of cystic fibrosis drugs and for studying the role of cilia in cholangiocyte development and function. Transplantation studies show that the mature cholangiocytes generate ductal structures in the liver of immunocompromised mice indicating that it may be possible to develop cell-based therapies to restore bile duct function in patients with biliary disease. Nature Publishing Group UK 2021-11-11 /pmc/articles/PMC8586142/ /pubmed/34764255 http://dx.doi.org/10.1038/s41467-021-26764-0 Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ogawa, Mina Jiang, Jia-Xin Xia, Sunny Yang, Donghe Ding, Avrilynn Laselva, Onofrio Hernandez, Marcela Cui, Changyi Higuchi, Yuichiro Suemizu, Hiroshi Dorrell, Craig Grompe, Markus Bear, Christine E. Ogawa, Shinichiro Generation of functional ciliated cholangiocytes from human pluripotent stem cells |
title | Generation of functional ciliated cholangiocytes from human pluripotent stem cells |
title_full | Generation of functional ciliated cholangiocytes from human pluripotent stem cells |
title_fullStr | Generation of functional ciliated cholangiocytes from human pluripotent stem cells |
title_full_unstemmed | Generation of functional ciliated cholangiocytes from human pluripotent stem cells |
title_short | Generation of functional ciliated cholangiocytes from human pluripotent stem cells |
title_sort | generation of functional ciliated cholangiocytes from human pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586142/ https://www.ncbi.nlm.nih.gov/pubmed/34764255 http://dx.doi.org/10.1038/s41467-021-26764-0 |
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