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Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells

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 differ...

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Autores principales: Okada, Kosuke, Fujimura, Takeki, Kikuchi, Takeshi, Aino, Makoto, Kamiya, Yosuke, Izawa, Ario, Iwamura, Yuki, Goto, Hisashi, Okabe, Iichiro, Miyake, Eriko, Hasegawa, Yoshiaki, Mogi, Makio, Mitani, Akio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314955/
https://www.ncbi.nlm.nih.gov/pubmed/28229025
http://dx.doi.org/10.7717/peerj.2999
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author Okada, Kosuke
Fujimura, Takeki
Kikuchi, Takeshi
Aino, Makoto
Kamiya, Yosuke
Izawa, Ario
Iwamura, Yuki
Goto, Hisashi
Okabe, Iichiro
Miyake, Eriko
Hasegawa, Yoshiaki
Mogi, Makio
Mitani, Akio
author_facet Okada, Kosuke
Fujimura, Takeki
Kikuchi, Takeshi
Aino, Makoto
Kamiya, Yosuke
Izawa, Ario
Iwamura, Yuki
Goto, Hisashi
Okabe, Iichiro
Miyake, Eriko
Hasegawa, Yoshiaki
Mogi, Makio
Mitani, Akio
author_sort Okada, Kosuke
collection PubMed
description 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 RORγt (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-1β, 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 RORCmRNA 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 RORα and RORγt inhibition and might play an important role in inflammatory diseases such as periodontitis.
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spelling pubmed-53149552017-02-22 Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells Okada, Kosuke Fujimura, Takeki Kikuchi, Takeshi Aino, Makoto Kamiya, Yosuke Izawa, Ario Iwamura, Yuki Goto, Hisashi Okabe, Iichiro Miyake, Eriko Hasegawa, Yoshiaki Mogi, Makio Mitani, Akio PeerJ Dentistry 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 RORγt (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-1β, 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 RORCmRNA 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 RORα and RORγt inhibition and might play an important role in inflammatory diseases such as periodontitis. PeerJ Inc. 2017-02-15 /pmc/articles/PMC5314955/ /pubmed/28229025 http://dx.doi.org/10.7717/peerj.2999 Text en ©2017 Okada et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Dentistry
Okada, Kosuke
Fujimura, Takeki
Kikuchi, Takeshi
Aino, Makoto
Kamiya, Yosuke
Izawa, Ario
Iwamura, Yuki
Goto, Hisashi
Okabe, Iichiro
Miyake, Eriko
Hasegawa, Yoshiaki
Mogi, Makio
Mitani, Akio
Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells
title Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells
title_full Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells
title_fullStr Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells
title_full_unstemmed Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells
title_short Effect of interleukin (IL)-35 on IL-17 expression and production by human CD4(+) T cells
title_sort effect of interleukin (il)-35 on il-17 expression and production by human cd4(+) t cells
topic Dentistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314955/
https://www.ncbi.nlm.nih.gov/pubmed/28229025
http://dx.doi.org/10.7717/peerj.2999
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