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

  • Tomoki Maekawa
  • , Kavita Hosur
  • , Toshiharu Abe
  • , Alpdogan Kantarci
  • , Athanasios Ziogas
  • , Baomei Wang
  • , Thomas E. Van Dyke
  • , Triantafyllos Chavakis
  • , George Hajishengallis

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish (US)
Article number8272
JournalNature communications
Volume6
DOIs
StatePublished - Sep 16 2015
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2015 Macmillan Publishers Limited. All rights reserved.

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