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A platform to reproducibly evaluate human colon permeability and damage
The intestinal epithelium comprises diverse cell types and executes many specialized functions as the primary interface between luminal contents and internal organs. A key function provided by the epithelium is maintenance of a barrier that protects the individual from pathogens, irritating luminal...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235044/ https://www.ncbi.nlm.nih.gov/pubmed/37264117 http://dx.doi.org/10.1038/s41598-023-36020-8 |
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author | Marr, Elizabeth E. Mulhern, Thomas J. Welch, Michaela Keegan, Philip Caballero-Franco, Celia Johnson, Bryce G. Kasaian, Marion Azizgolshani, Hesham Petrie, Timothy Charest, Joseph Wiellette, Elizabeth |
author_facet | Marr, Elizabeth E. Mulhern, Thomas J. Welch, Michaela Keegan, Philip Caballero-Franco, Celia Johnson, Bryce G. Kasaian, Marion Azizgolshani, Hesham Petrie, Timothy Charest, Joseph Wiellette, Elizabeth |
author_sort | Marr, Elizabeth E. |
collection | PubMed |
description | The intestinal epithelium comprises diverse cell types and executes many specialized functions as the primary interface between luminal contents and internal organs. A key function provided by the epithelium is maintenance of a barrier that protects the individual from pathogens, irritating luminal contents, and the microbiota. Disruption of this barrier can lead to inflammatory disease within the intestinal mucosa, and, in more severe cases, to sepsis. Animal models to study intestinal permeability are costly and not entirely predictive of human biology. Here we present a model of human colon barrier function that integrates primary human colon stem cells into Draper’s PREDICT96 microfluidic organ-on-chip platform to yield a high-throughput system appropriate to predict damage and healing of the human colon epithelial barrier. We have demonstrated pharmacologically induced barrier damage measured by both a high throughput molecular permeability assay and transepithelial resistance. Using these assays, we developed an Inflammatory Bowel Disease-relevant model through cytokine induced damage that can support studies of disease mechanisms and putative therapeutics. |
format | Online Article Text |
id | pubmed-10235044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102350442023-06-03 A platform to reproducibly evaluate human colon permeability and damage Marr, Elizabeth E. Mulhern, Thomas J. Welch, Michaela Keegan, Philip Caballero-Franco, Celia Johnson, Bryce G. Kasaian, Marion Azizgolshani, Hesham Petrie, Timothy Charest, Joseph Wiellette, Elizabeth Sci Rep Article The intestinal epithelium comprises diverse cell types and executes many specialized functions as the primary interface between luminal contents and internal organs. A key function provided by the epithelium is maintenance of a barrier that protects the individual from pathogens, irritating luminal contents, and the microbiota. Disruption of this barrier can lead to inflammatory disease within the intestinal mucosa, and, in more severe cases, to sepsis. Animal models to study intestinal permeability are costly and not entirely predictive of human biology. Here we present a model of human colon barrier function that integrates primary human colon stem cells into Draper’s PREDICT96 microfluidic organ-on-chip platform to yield a high-throughput system appropriate to predict damage and healing of the human colon epithelial barrier. We have demonstrated pharmacologically induced barrier damage measured by both a high throughput molecular permeability assay and transepithelial resistance. Using these assays, we developed an Inflammatory Bowel Disease-relevant model through cytokine induced damage that can support studies of disease mechanisms and putative therapeutics. Nature Publishing Group UK 2023-06-01 /pmc/articles/PMC10235044/ /pubmed/37264117 http://dx.doi.org/10.1038/s41598-023-36020-8 Text en © The Author(s) 2023 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 Marr, Elizabeth E. Mulhern, Thomas J. Welch, Michaela Keegan, Philip Caballero-Franco, Celia Johnson, Bryce G. Kasaian, Marion Azizgolshani, Hesham Petrie, Timothy Charest, Joseph Wiellette, Elizabeth A platform to reproducibly evaluate human colon permeability and damage |
title | A platform to reproducibly evaluate human colon permeability and damage |
title_full | A platform to reproducibly evaluate human colon permeability and damage |
title_fullStr | A platform to reproducibly evaluate human colon permeability and damage |
title_full_unstemmed | A platform to reproducibly evaluate human colon permeability and damage |
title_short | A platform to reproducibly evaluate human colon permeability and damage |
title_sort | platform to reproducibly evaluate human colon permeability and damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235044/ https://www.ncbi.nlm.nih.gov/pubmed/37264117 http://dx.doi.org/10.1038/s41598-023-36020-8 |
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