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Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication
Through pluripotent stem cell (PSC) technology, human intestinal organoids (HIOs) with remarkably similarity to the fetal intestine in cellular composition, architecture, and absorptive/secretory functions have been successfully developed, providing a useful in vitro model system to study the struct...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626734/ https://www.ncbi.nlm.nih.gov/pubmed/28974702 http://dx.doi.org/10.1038/s41598-017-12736-2 |
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author | Zhang, Dongsheng Tan, Ming Zhong, Weiming Xia, Ming Huang, Pengwei Jiang, Xi |
author_facet | Zhang, Dongsheng Tan, Ming Zhong, Weiming Xia, Ming Huang, Pengwei Jiang, Xi |
author_sort | Zhang, Dongsheng |
collection | PubMed |
description | Through pluripotent stem cell (PSC) technology, human intestinal organoids (HIOs) with remarkably similarity to the fetal intestine in cellular composition, architecture, and absorptive/secretory functions have been successfully developed, providing a useful in vitro model system to study the structure and function of human congenital gut and intestinally related diseases. We report here the usefulness of HIOs as a model system to study intestinal carbohydrate expression, virus-host interaction, and replication of human noroviruses (huNoVs). We found that fully developed HIOs express effectively various types 1 and 2 HBGAs, including Lewis, secretor, and nonsecretor antigens, distributing on the glycocalyx. Selected huNoV-like particles (VLPs) bound the glycocalyx of HIOs with matched HBGA phenotypes. Using GII.4 huNoV positive stool filtrates, we demonstrated limited huNoV replication in HIOs with corresponding HBGAs through detection of viral RNAs by RT-PCR and capsid antigens by immunostaining methods. Our data suggested that, after further improvements, HIOs can be a useful model to study intestinal glycan expression, huNoV-intestine interaction, and huNoV infection in the intestine. |
format | Online Article Text |
id | pubmed-5626734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56267342017-10-12 Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication Zhang, Dongsheng Tan, Ming Zhong, Weiming Xia, Ming Huang, Pengwei Jiang, Xi Sci Rep Article Through pluripotent stem cell (PSC) technology, human intestinal organoids (HIOs) with remarkably similarity to the fetal intestine in cellular composition, architecture, and absorptive/secretory functions have been successfully developed, providing a useful in vitro model system to study the structure and function of human congenital gut and intestinally related diseases. We report here the usefulness of HIOs as a model system to study intestinal carbohydrate expression, virus-host interaction, and replication of human noroviruses (huNoVs). We found that fully developed HIOs express effectively various types 1 and 2 HBGAs, including Lewis, secretor, and nonsecretor antigens, distributing on the glycocalyx. Selected huNoV-like particles (VLPs) bound the glycocalyx of HIOs with matched HBGA phenotypes. Using GII.4 huNoV positive stool filtrates, we demonstrated limited huNoV replication in HIOs with corresponding HBGAs through detection of viral RNAs by RT-PCR and capsid antigens by immunostaining methods. Our data suggested that, after further improvements, HIOs can be a useful model to study intestinal glycan expression, huNoV-intestine interaction, and huNoV infection in the intestine. Nature Publishing Group UK 2017-10-03 /pmc/articles/PMC5626734/ /pubmed/28974702 http://dx.doi.org/10.1038/s41598-017-12736-2 Text en © The Author(s) 2017 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 Zhang, Dongsheng Tan, Ming Zhong, Weiming Xia, Ming Huang, Pengwei Jiang, Xi Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication |
title | Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication |
title_full | Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication |
title_fullStr | Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication |
title_full_unstemmed | Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication |
title_short | Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication |
title_sort | human intestinal organoids express histo-blood group antigens, bind norovirus vlps, and support limited norovirus replication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626734/ https://www.ncbi.nlm.nih.gov/pubmed/28974702 http://dx.doi.org/10.1038/s41598-017-12736-2 |
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