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Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip
Studies on human intestinal injury induced by acute exposure to γ-radiation commonly rely on use of animal models because culture systems do not faithfully mimic human intestinal physiology. Here we used a human Gut-on-a-Chip (Gut Chip) microfluidic device lined by human intestinal epithelial cells...
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/PMC5833800/ https://www.ncbi.nlm.nih.gov/pubmed/29445080 http://dx.doi.org/10.1038/s41419-018-0304-8 |
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author | Jalili-Firoozinezhad, Sasan Prantil-Baun, Rachelle Jiang, Amanda Potla, Ratnakar Mammoto, Tadanori Weaver, James C. Ferrante, Thomas C. Kim, Hyun Jung Cabral, Joaquim M. S. Levy, Oren Ingber, Donald E. |
author_facet | Jalili-Firoozinezhad, Sasan Prantil-Baun, Rachelle Jiang, Amanda Potla, Ratnakar Mammoto, Tadanori Weaver, James C. Ferrante, Thomas C. Kim, Hyun Jung Cabral, Joaquim M. S. Levy, Oren Ingber, Donald E. |
author_sort | Jalili-Firoozinezhad, Sasan |
collection | PubMed |
description | Studies on human intestinal injury induced by acute exposure to γ-radiation commonly rely on use of animal models because culture systems do not faithfully mimic human intestinal physiology. Here we used a human Gut-on-a-Chip (Gut Chip) microfluidic device lined by human intestinal epithelial cells and vascular endothelial cells to model radiation injury and assess the efficacy of radiation countermeasure drugs in vitro. Exposure of the Gut Chip to γ-radiation resulted in increased generation of reactive oxygen species, cytotoxicity, apoptosis, and DNA fragmentation, as well as villus blunting, disruption of tight junctions, and compromise of intestinal barrier integrity. In contrast, pre-treatment with a potential prophylactic radiation countermeasure drug, dimethyloxaloylglycine (DMOG), significantly suppressed all of these injury responses. Thus, the human Gut Chip may serve as an in vitro platform for studying radiation-induced cell death and associate gastrointestinal acute syndrome, in addition to screening of novel radio-protective medical countermeasure drugs. |
format | Online Article Text |
id | pubmed-5833800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58338002018-03-06 Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip Jalili-Firoozinezhad, Sasan Prantil-Baun, Rachelle Jiang, Amanda Potla, Ratnakar Mammoto, Tadanori Weaver, James C. Ferrante, Thomas C. Kim, Hyun Jung Cabral, Joaquim M. S. Levy, Oren Ingber, Donald E. Cell Death Dis Article Studies on human intestinal injury induced by acute exposure to γ-radiation commonly rely on use of animal models because culture systems do not faithfully mimic human intestinal physiology. Here we used a human Gut-on-a-Chip (Gut Chip) microfluidic device lined by human intestinal epithelial cells and vascular endothelial cells to model radiation injury and assess the efficacy of radiation countermeasure drugs in vitro. Exposure of the Gut Chip to γ-radiation resulted in increased generation of reactive oxygen species, cytotoxicity, apoptosis, and DNA fragmentation, as well as villus blunting, disruption of tight junctions, and compromise of intestinal barrier integrity. In contrast, pre-treatment with a potential prophylactic radiation countermeasure drug, dimethyloxaloylglycine (DMOG), significantly suppressed all of these injury responses. Thus, the human Gut Chip may serve as an in vitro platform for studying radiation-induced cell death and associate gastrointestinal acute syndrome, in addition to screening of novel radio-protective medical countermeasure drugs. Nature Publishing Group UK 2018-02-14 /pmc/articles/PMC5833800/ /pubmed/29445080 http://dx.doi.org/10.1038/s41419-018-0304-8 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 Jalili-Firoozinezhad, Sasan Prantil-Baun, Rachelle Jiang, Amanda Potla, Ratnakar Mammoto, Tadanori Weaver, James C. Ferrante, Thomas C. Kim, Hyun Jung Cabral, Joaquim M. S. Levy, Oren Ingber, Donald E. Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip |
title | Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip |
title_full | Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip |
title_fullStr | Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip |
title_full_unstemmed | Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip |
title_short | Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip |
title_sort | modeling radiation injury-induced cell death and countermeasure drug responses in a human gut-on-a-chip |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833800/ https://www.ncbi.nlm.nih.gov/pubmed/29445080 http://dx.doi.org/10.1038/s41419-018-0304-8 |
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