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IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration

Monocytes are actively recruited at sites of chronic inflammation. However, molecular factors involved in this process are not fully elucidated. Here, we show that cytokine IL-4 which is implicated in the development of chronic inflammatory disease atopic dermatitis (AD) induces expression of transc...

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Autores principales: Ovsiy, Ilja, Riabov, Vladimir, Manousaridis, Ioannis, Michel, Julia, Moganti, Kondaiah, Yin, Shuiping, Liu, Tengfei, Sticht, Carsten, Kremmer, Elisabeth, Harmsen, Martin C., Goerdt, Sergij, Gratchev, Alexei, Kzhyshkowska, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715145/
https://www.ncbi.nlm.nih.gov/pubmed/29203829
http://dx.doi.org/10.1038/s41598-017-17307-z
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author Ovsiy, Ilja
Riabov, Vladimir
Manousaridis, Ioannis
Michel, Julia
Moganti, Kondaiah
Yin, Shuiping
Liu, Tengfei
Sticht, Carsten
Kremmer, Elisabeth
Harmsen, Martin C.
Goerdt, Sergij
Gratchev, Alexei
Kzhyshkowska, Julia
author_facet Ovsiy, Ilja
Riabov, Vladimir
Manousaridis, Ioannis
Michel, Julia
Moganti, Kondaiah
Yin, Shuiping
Liu, Tengfei
Sticht, Carsten
Kremmer, Elisabeth
Harmsen, Martin C.
Goerdt, Sergij
Gratchev, Alexei
Kzhyshkowska, Julia
author_sort Ovsiy, Ilja
collection PubMed
description Monocytes are actively recruited at sites of chronic inflammation. However, molecular factors involved in this process are not fully elucidated. Here, we show that cytokine IL-4 which is implicated in the development of chronic inflammatory disease atopic dermatitis (AD) induces expression of transcription factor FoxQ1 in human monocytes and macrophages. FoxQ1 mRNA levels were elevated in monocytes of AD patients compared to healthy donors. Overexpression of FoxQ1 in RAW 264.7 monocytic cells facilitated their migration towards MCP-1 and was associated with decreased expression of migration-regulating genes (claudin 11 and plexin C1). Furthermore, FoxQ1 overexpression in RAW cells accelerated TNFα secretion after LPS challenge. Overall, our results indicate that FoxQ1 stimulates monocyte motility, increases pro-inflammatory potential, and directs monocyte migration towards MCP-1 that is crucial for monocyte influx into inflammatory sites. This mechanism could contribute to the pathogenesis of chronic inflammatory disorders such as AD.
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spelling pubmed-57151452017-12-08 IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration Ovsiy, Ilja Riabov, Vladimir Manousaridis, Ioannis Michel, Julia Moganti, Kondaiah Yin, Shuiping Liu, Tengfei Sticht, Carsten Kremmer, Elisabeth Harmsen, Martin C. Goerdt, Sergij Gratchev, Alexei Kzhyshkowska, Julia Sci Rep Article Monocytes are actively recruited at sites of chronic inflammation. However, molecular factors involved in this process are not fully elucidated. Here, we show that cytokine IL-4 which is implicated in the development of chronic inflammatory disease atopic dermatitis (AD) induces expression of transcription factor FoxQ1 in human monocytes and macrophages. FoxQ1 mRNA levels were elevated in monocytes of AD patients compared to healthy donors. Overexpression of FoxQ1 in RAW 264.7 monocytic cells facilitated their migration towards MCP-1 and was associated with decreased expression of migration-regulating genes (claudin 11 and plexin C1). Furthermore, FoxQ1 overexpression in RAW cells accelerated TNFα secretion after LPS challenge. Overall, our results indicate that FoxQ1 stimulates monocyte motility, increases pro-inflammatory potential, and directs monocyte migration towards MCP-1 that is crucial for monocyte influx into inflammatory sites. This mechanism could contribute to the pathogenesis of chronic inflammatory disorders such as AD. Nature Publishing Group UK 2017-12-04 /pmc/articles/PMC5715145/ /pubmed/29203829 http://dx.doi.org/10.1038/s41598-017-17307-z Text en © The Author(s) 2017 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
Ovsiy, Ilja
Riabov, Vladimir
Manousaridis, Ioannis
Michel, Julia
Moganti, Kondaiah
Yin, Shuiping
Liu, Tengfei
Sticht, Carsten
Kremmer, Elisabeth
Harmsen, Martin C.
Goerdt, Sergij
Gratchev, Alexei
Kzhyshkowska, Julia
IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
title IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
title_full IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
title_fullStr IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
title_full_unstemmed IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
title_short IL-4 driven transcription factor FoxQ1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
title_sort il-4 driven transcription factor foxq1 is expressed by monocytes in atopic dermatitis and stimulates monocyte migration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715145/
https://www.ncbi.nlm.nih.gov/pubmed/29203829
http://dx.doi.org/10.1038/s41598-017-17307-z
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