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HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6

NF-κB signalling is crucial for cellular responses to inflammation but is also associated with the hypoxia response. NF-κB and hypoxia inducible factor (HIF) transcription factors possess an intense molecular crosstalk. Although it is known that HIF-1α modulates NF-κB transcriptional response, very...

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Detalles Bibliográficos
Autores principales: D’Ignazio, Laura, Shakir, Dilem, Batie, Michael, Muller, H. Arno, Rocha, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216149/
https://www.ncbi.nlm.nih.gov/pubmed/32344511
http://dx.doi.org/10.3390/ijms21083000
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author D’Ignazio, Laura
Shakir, Dilem
Batie, Michael
Muller, H. Arno
Rocha, Sonia
author_facet D’Ignazio, Laura
Shakir, Dilem
Batie, Michael
Muller, H. Arno
Rocha, Sonia
author_sort D’Ignazio, Laura
collection PubMed
description NF-κB signalling is crucial for cellular responses to inflammation but is also associated with the hypoxia response. NF-κB and hypoxia inducible factor (HIF) transcription factors possess an intense molecular crosstalk. Although it is known that HIF-1α modulates NF-κB transcriptional response, very little is understood regarding how HIF-1β contributes to NF-κB signalling. Here, we demonstrate that HIF-1β is required for full NF-κB activation in cells following canonical and non-canonical stimuli. We found that HIF-1β specifically controls TRAF6 expression in human cells but also in Drosophila melanogaster. HIF-1β binds to the TRAF6 gene and controls its expression independently of HIF-1α. Furthermore, exogenous TRAF6 expression is able to rescue all of the cellular phenotypes observed in the absence of HIF-1β. These results indicate that HIF-1β is an important regulator of NF-κB with consequences for homeostasis and human disease.
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spelling pubmed-72161492020-05-22 HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6 D’Ignazio, Laura Shakir, Dilem Batie, Michael Muller, H. Arno Rocha, Sonia Int J Mol Sci Article NF-κB signalling is crucial for cellular responses to inflammation but is also associated with the hypoxia response. NF-κB and hypoxia inducible factor (HIF) transcription factors possess an intense molecular crosstalk. Although it is known that HIF-1α modulates NF-κB transcriptional response, very little is understood regarding how HIF-1β contributes to NF-κB signalling. Here, we demonstrate that HIF-1β is required for full NF-κB activation in cells following canonical and non-canonical stimuli. We found that HIF-1β specifically controls TRAF6 expression in human cells but also in Drosophila melanogaster. HIF-1β binds to the TRAF6 gene and controls its expression independently of HIF-1α. Furthermore, exogenous TRAF6 expression is able to rescue all of the cellular phenotypes observed in the absence of HIF-1β. These results indicate that HIF-1β is an important regulator of NF-κB with consequences for homeostasis and human disease. MDPI 2020-04-24 /pmc/articles/PMC7216149/ /pubmed/32344511 http://dx.doi.org/10.3390/ijms21083000 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
D’Ignazio, Laura
Shakir, Dilem
Batie, Michael
Muller, H. Arno
Rocha, Sonia
HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6
title HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6
title_full HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6
title_fullStr HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6
title_full_unstemmed HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6
title_short HIF-1β Positively Regulates NF-κB Activity via Direct Control of TRAF6
title_sort hif-1β positively regulates nf-κb activity via direct control of traf6
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216149/
https://www.ncbi.nlm.nih.gov/pubmed/32344511
http://dx.doi.org/10.3390/ijms21083000
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