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Functional characterization of IL-17F as a selective neutrophil attractant in psoriasis

  • Hideaki Watanabe
  • , Mio Kawaguchi
  • , Sawa Fujishima
  • , Miyoko Ogura
  • , Satoshi Matsukura
  • , Hiroko Takeuchi
  • , Motoi Ohba
  • , Hirohiko Sueki
  • , Fumio Kokubu
  • , Nobuyuki Hizawa
  • , Mitsuru Adachi
  • , Shau Ku Huang
  • , Masafumi Iijima

Research output: Contribution to journalArticlepeer-review

Abstract

IL-17F is known to be involved in many inflammatory diseases, but its role in skin diseases has not been fully examined. Because IL-8 is involved in many skin diseases such as psoriasis, we investigated the production of IL-8 in normal human epidermal keratinocytes (NHEKs) stimulated by IL-17F, tumor necrosis factor-α (TNF-α), IL-17A, and control using real-time PCR and ELISA. The results showed that IL-17F induced production of IL-8 in NHEKs in a time-dependent manner. Interestingly, the amounts of IL-8 stimulated by IL-17F were much higher than those stimulated by TNF-α or IL-17A. Next, we confirmed that selective mitogen-activated protein kinase kinase inhibitors significantly inhibited IL-17F-induced IL-8 production. Moreover, mouse skin intradermally injected with IL-17F expressed high level of IL-8 mRNA and induced ERK1/2 phosphorylation. Histological examination of mouse skin that was injected with IL-17F revealed marked neutrophilia in dermis and the infiltration was significantly inhibited by anti-IL-8 antibody. Finally, IL-17F expression in skin biopsy samples from psoriasis patients were examined by western blotting and ELISA. IL-17F was upregulated in lesional psoriatic skin compared with nonlesional skin. These results indicate that IL-17F may be involved in psoriasis via, in part, the activation of ERK1/2 and the induction of IL-8 in keratinocytes.

Original languageEnglish
Pages (from-to)650-656
Number of pages7
JournalJournal of Investigative Dermatology
Volume129
Issue number3
DOIs
Publication statusPublished - Mar 2009

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Dermatology
  • Cell Biology

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