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Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses
Tumour necrosis factor (TNF) is a key cytokine during inflammatory responses and its dysregulation is detrimental in many inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease. Here, we used a bacterial artificial chromosome (BAC) construct that expresses luciferase unde...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336827/ https://www.ncbi.nlm.nih.gov/pubmed/30655563 http://dx.doi.org/10.1038/s41598-018-36969-x |
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author | Minshawi, Faisal White, Mike R. H. Muller, Werner Humphreys, Neil Jackson, Dean Campbell, Barry J. Adamson, Antony Papoutsopoulou, Stamatia |
author_facet | Minshawi, Faisal White, Mike R. H. Muller, Werner Humphreys, Neil Jackson, Dean Campbell, Barry J. Adamson, Antony Papoutsopoulou, Stamatia |
author_sort | Minshawi, Faisal |
collection | PubMed |
description | Tumour necrosis factor (TNF) is a key cytokine during inflammatory responses and its dysregulation is detrimental in many inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease. Here, we used a bacterial artificial chromosome (BAC) construct that expresses luciferase under the control of the human TNF locus to generate a novel transgenic mouse, the hTNF.LucBAC strain. In vitro stimulation of hTNF.LucBAC cells of different origin revealed a cell specific response to stimuli demonstrating the integrated construct’s ability as a proxy for inflammatory gene response. Lipopolysaccharide was the most potent luciferase inducer in macrophages, while TNF was a strong activator in intestinal organoids. Lipopolysaccharide-induced luciferase activity in macrophages was downregulated by inhibitors of NF-κB pathway, as well as by Interleukin-10, a known anti-inflammatory cytokine. Moreover, the transgene-dependent luciferase activity showed a positive correlation to the endogenous murine soluble TNF secreted to the culture medium. In conclusion, the hTNF.LucBAC strain is a valuable tool for studying and screening molecules that target TNF synthesis and will allow further functional studies of the regulatory elements of the TNF locus. |
format | Online Article Text |
id | pubmed-6336827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63368272019-01-22 Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses Minshawi, Faisal White, Mike R. H. Muller, Werner Humphreys, Neil Jackson, Dean Campbell, Barry J. Adamson, Antony Papoutsopoulou, Stamatia Sci Rep Article Tumour necrosis factor (TNF) is a key cytokine during inflammatory responses and its dysregulation is detrimental in many inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease. Here, we used a bacterial artificial chromosome (BAC) construct that expresses luciferase under the control of the human TNF locus to generate a novel transgenic mouse, the hTNF.LucBAC strain. In vitro stimulation of hTNF.LucBAC cells of different origin revealed a cell specific response to stimuli demonstrating the integrated construct’s ability as a proxy for inflammatory gene response. Lipopolysaccharide was the most potent luciferase inducer in macrophages, while TNF was a strong activator in intestinal organoids. Lipopolysaccharide-induced luciferase activity in macrophages was downregulated by inhibitors of NF-κB pathway, as well as by Interleukin-10, a known anti-inflammatory cytokine. Moreover, the transgene-dependent luciferase activity showed a positive correlation to the endogenous murine soluble TNF secreted to the culture medium. In conclusion, the hTNF.LucBAC strain is a valuable tool for studying and screening molecules that target TNF synthesis and will allow further functional studies of the regulatory elements of the TNF locus. Nature Publishing Group UK 2019-01-17 /pmc/articles/PMC6336827/ /pubmed/30655563 http://dx.doi.org/10.1038/s41598-018-36969-x Text en © The Author(s) 2019 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 Minshawi, Faisal White, Mike R. H. Muller, Werner Humphreys, Neil Jackson, Dean Campbell, Barry J. Adamson, Antony Papoutsopoulou, Stamatia Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses |
title | Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses |
title_full | Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses |
title_fullStr | Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses |
title_full_unstemmed | Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses |
title_short | Human TNF-Luc reporter mouse: A new model to quantify inflammatory responses |
title_sort | human tnf-luc reporter mouse: a new model to quantify inflammatory responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336827/ https://www.ncbi.nlm.nih.gov/pubmed/30655563 http://dx.doi.org/10.1038/s41598-018-36969-x |
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