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Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4+ T cells
Author(s) -
Kosuke Okada,
Takeki Fujimura,
Takeshi Kikuchi,
Makoto Aino,
Yosuke Kamiya,
Ario Izawa,
Yuki Iwamura,
Hisashi Goto,
Iichiro Okabe,
Eriko Miyake,
Yoshiaki Hasegawa,
Makio Mogi,
Akio Mitani
Publication year - 2017
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.2999
Subject(s) - rar related orphan receptor gamma , interleukin 17 , peripheral blood mononuclear cell , orphan receptor , foxp3 , retinoic acid , cytokine , flow cytometry , interleukin , population , immunology , t helper cell , biology , chemistry , microbiology and biotechnology , t cell , medicine , cell culture , immune system , in vitro , biochemistry , transcription factor , genetics , environmental health , gene
Background Interleukin (IL)-17 produced by mainly T helper 17 (Th17) cells may play an important destructive role in chronic periodontitis (CP). Thus, anti-inflammatory cytokines, such as IL-35, might have a beneficial effect in periodontitis by inhibiting differentiation of Th17 cells. Th17 differentiation is regulated by the retinoic acid receptor-related orphan receptor (ROR) α (encoded by RORA ) and ROR γ t (encoded by RORC ). However, the role of IL-35 in periodontitis is not clear and the effect of IL-35 on the function of Th17 cells is still incompletely understood. Therefore, we investigated the effects of IL-35 on Th17 cells. Methods Peripheral blood mononuclear cells (PBMCs) were sampled from three healthy volunteers and three CP patients and were analyzed by flow cytometry for T cell population. Th17 cells differentiated by a cytokine cocktail (recombinant transforming growth factor- β , rIL-6, rIL-1 β , anti-interferon (IFN)- γ , anti-IL-2 and anti-IL-4) from PBMCs were cultured with or without rIL-35. IL17A (which usually refers to IL-17), RORA and RORC mRNA expression was analyzed by quantitative polymerase chain reaction, and IL-17A production was determined by enzyme-linked immunosorbent assay. Results The proportion of IL-17A + CD4 + slightly increased in CP patients compared with healthy controls, however, there were no significant differences in the percentage of IL-17A + CD4 + as well as IFN- γ + CD4 + and Foxp3 + CD4 + T cells between healthy controls and CP patients. IL17A , RORA and RORC mRNA expression was significantly increased in Th17 cells induced by the cytokine cocktail, and the induction was significantly inhibited by addition of rIL-35 (1 ng/mL). IL-17A production in Th17 cells was significantly inhibited by rIL-35 addition (1 ng/mL). Discussion The present study suggests that IL-35 could directly suppress IL-17 expression via ROR α and ROR γ t inhibition and might play an important role in inflammatory diseases such as periodontitis.

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