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Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway

Del-1 is an endothelial cell-secreted anti-inflammatory protein. In humans and mice, Del-1 expression is inversely related to that of IL-17, which inhibits Del-1 through hitherto unidentified mechanism(s). Here we show that IL-17 downregulates human endothelial cell expression of Del-1 by targeting...

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Autores principales: Maekawa, Tomoki, Hosur, Kavita, Abe, Toshiharu, Kantarci, Alpdogan, Ziogas, Athanasios, Wang, Baomei, Van Dyke, Thomas E., Chavakis, Triantafyllos, Hajishengallis, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573473/
https://www.ncbi.nlm.nih.gov/pubmed/26374165
http://dx.doi.org/10.1038/ncomms9272
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author Maekawa, Tomoki
Hosur, Kavita
Abe, Toshiharu
Kantarci, Alpdogan
Ziogas, Athanasios
Wang, Baomei
Van Dyke, Thomas E.
Chavakis, Triantafyllos
Hajishengallis, George
author_facet Maekawa, Tomoki
Hosur, Kavita
Abe, Toshiharu
Kantarci, Alpdogan
Ziogas, Athanasios
Wang, Baomei
Van Dyke, Thomas E.
Chavakis, Triantafyllos
Hajishengallis, George
author_sort Maekawa, Tomoki
collection PubMed
description Del-1 is an endothelial cell-secreted anti-inflammatory protein. In humans and mice, Del-1 expression is inversely related to that of IL-17, which inhibits Del-1 through hitherto unidentified mechanism(s). Here we show that IL-17 downregulates human endothelial cell expression of Del-1 by targeting a critical transcription factor, C/EBPβ. Specifically, IL-17 causes GSK-3β-dependent phosphorylation of C/EBPβ, which is associated with diminished C/EBPβ binding to the Del-1 promoter and suppressed Del-1 expression. This inhibitory action of IL-17 can be reversed at the GSK-3β level by PI3K/Akt signalling induced by D-resolvins. The biological relevance of this regulatory network is confirmed in a mouse model of inflammatory periodontitis. Intriguingly, resolvin-D1 (RvD1) confers protection against IL-17-driven periodontal bone loss in a Del-1-dependent manner, indicating an RvD1-Del-1 axis against IL-17-induced pathological inflammation. The dissection of signalling pathways regulating Del-1 expression provides potential targets to treat inflammatory diseases associated with diminished Del-1 expression, such as periodontitis and multiple sclerosis.
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spelling pubmed-45734732015-10-21 Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway Maekawa, Tomoki Hosur, Kavita Abe, Toshiharu Kantarci, Alpdogan Ziogas, Athanasios Wang, Baomei Van Dyke, Thomas E. Chavakis, Triantafyllos Hajishengallis, George Nat Commun Article Del-1 is an endothelial cell-secreted anti-inflammatory protein. In humans and mice, Del-1 expression is inversely related to that of IL-17, which inhibits Del-1 through hitherto unidentified mechanism(s). Here we show that IL-17 downregulates human endothelial cell expression of Del-1 by targeting a critical transcription factor, C/EBPβ. Specifically, IL-17 causes GSK-3β-dependent phosphorylation of C/EBPβ, which is associated with diminished C/EBPβ binding to the Del-1 promoter and suppressed Del-1 expression. This inhibitory action of IL-17 can be reversed at the GSK-3β level by PI3K/Akt signalling induced by D-resolvins. The biological relevance of this regulatory network is confirmed in a mouse model of inflammatory periodontitis. Intriguingly, resolvin-D1 (RvD1) confers protection against IL-17-driven periodontal bone loss in a Del-1-dependent manner, indicating an RvD1-Del-1 axis against IL-17-induced pathological inflammation. The dissection of signalling pathways regulating Del-1 expression provides potential targets to treat inflammatory diseases associated with diminished Del-1 expression, such as periodontitis and multiple sclerosis. Nature Pub. Group 2015-09-16 /pmc/articles/PMC4573473/ /pubmed/26374165 http://dx.doi.org/10.1038/ncomms9272 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Maekawa, Tomoki
Hosur, Kavita
Abe, Toshiharu
Kantarci, Alpdogan
Ziogas, Athanasios
Wang, Baomei
Van Dyke, Thomas E.
Chavakis, Triantafyllos
Hajishengallis, George
Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
title Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
title_full Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
title_fullStr Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
title_full_unstemmed Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
title_short Antagonistic effects of IL-17 and D-resolvins on endothelial Del-1 expression through a GSK-3β-C/EBPβ pathway
title_sort antagonistic effects of il-17 and d-resolvins on endothelial del-1 expression through a gsk-3β-c/ebpβ pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573473/
https://www.ncbi.nlm.nih.gov/pubmed/26374165
http://dx.doi.org/10.1038/ncomms9272
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