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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...

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Autores principales: Minshawi, Faisal, White, Mike R. H., Muller, Werner, Humphreys, Neil, Jackson, Dean, Campbell, Barry J., Adamson, Antony, Papoutsopoulou, Stamatia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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