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Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids
Human pluripotent stem cell (hPSC)-derived intestinal organoids (hIOs) form 3D structures organized into crypt and villus domains, making them an excellent in vitro model system for studying human intestinal development and disease. However, hPSC-derived hIOs still require in vivo maturation to full...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072745/ https://www.ncbi.nlm.nih.gov/pubmed/30072687 http://dx.doi.org/10.1038/s41467-018-05450-8 |
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author | Jung, Kwang Bo Lee, Hana Son, Ye Seul Lee, Mi-Ok Kim, Young-Dae Oh, Soo Jin Kwon, Ohman Cho, Sunwha Cho, Hyun-Soo Kim, Dae-Soo Oh, Jung-Hwa Zilbauer, Matthias Min, Jeong-Ki Jung, Cho-Rok Kim, Janghwan Son, Mi-Young |
author_facet | Jung, Kwang Bo Lee, Hana Son, Ye Seul Lee, Mi-Ok Kim, Young-Dae Oh, Soo Jin Kwon, Ohman Cho, Sunwha Cho, Hyun-Soo Kim, Dae-Soo Oh, Jung-Hwa Zilbauer, Matthias Min, Jeong-Ki Jung, Cho-Rok Kim, Janghwan Son, Mi-Young |
author_sort | Jung, Kwang Bo |
collection | PubMed |
description | Human pluripotent stem cell (hPSC)-derived intestinal organoids (hIOs) form 3D structures organized into crypt and villus domains, making them an excellent in vitro model system for studying human intestinal development and disease. However, hPSC-derived hIOs still require in vivo maturation to fully recapitulate adult intestine, with the mechanism of maturation remaining elusive. Here, we show that the co-culture with human T lymphocytes induce the in vitro maturation of hIOs, and identify STAT3-activating interleukin-2 (IL-2) as the major factor inducing maturation. hIOs exposed to IL-2 closely mimic the adult intestinal epithelium and have comparable expression levels of mature intestinal markers, as well as increased intestine-specific functional activities. Even after in vivo engraftment, in vitro-matured hIOs retain their maturation status. The results of our study demonstrate that STAT3 signaling can induce the maturation of hIOs in vitro, thereby circumventing the need for animal models and in vivo maturation. |
format | Online Article Text |
id | pubmed-6072745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60727452018-08-06 Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids Jung, Kwang Bo Lee, Hana Son, Ye Seul Lee, Mi-Ok Kim, Young-Dae Oh, Soo Jin Kwon, Ohman Cho, Sunwha Cho, Hyun-Soo Kim, Dae-Soo Oh, Jung-Hwa Zilbauer, Matthias Min, Jeong-Ki Jung, Cho-Rok Kim, Janghwan Son, Mi-Young Nat Commun Article Human pluripotent stem cell (hPSC)-derived intestinal organoids (hIOs) form 3D structures organized into crypt and villus domains, making them an excellent in vitro model system for studying human intestinal development and disease. However, hPSC-derived hIOs still require in vivo maturation to fully recapitulate adult intestine, with the mechanism of maturation remaining elusive. Here, we show that the co-culture with human T lymphocytes induce the in vitro maturation of hIOs, and identify STAT3-activating interleukin-2 (IL-2) as the major factor inducing maturation. hIOs exposed to IL-2 closely mimic the adult intestinal epithelium and have comparable expression levels of mature intestinal markers, as well as increased intestine-specific functional activities. Even after in vivo engraftment, in vitro-matured hIOs retain their maturation status. The results of our study demonstrate that STAT3 signaling can induce the maturation of hIOs in vitro, thereby circumventing the need for animal models and in vivo maturation. Nature Publishing Group UK 2018-08-02 /pmc/articles/PMC6072745/ /pubmed/30072687 http://dx.doi.org/10.1038/s41467-018-05450-8 Text en © The Author(s) 2018 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 Jung, Kwang Bo Lee, Hana Son, Ye Seul Lee, Mi-Ok Kim, Young-Dae Oh, Soo Jin Kwon, Ohman Cho, Sunwha Cho, Hyun-Soo Kim, Dae-Soo Oh, Jung-Hwa Zilbauer, Matthias Min, Jeong-Ki Jung, Cho-Rok Kim, Janghwan Son, Mi-Young Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
title | Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
title_full | Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
title_fullStr | Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
title_full_unstemmed | Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
title_short | Interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
title_sort | interleukin-2 induces the in vitro maturation of human pluripotent stem cell-derived intestinal organoids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072745/ https://www.ncbi.nlm.nih.gov/pubmed/30072687 http://dx.doi.org/10.1038/s41467-018-05450-8 |
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