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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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.
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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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