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Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling

Indoleamine 2,3-dioxygenase 2 (Ido2) is a recently identified catalytic enzyme in the tryptophan-kynurenine pathway that is expressed primarily in monocytes and dendritic cells. To elucidate the biological role of Ido2 in immune function, we introduced lipopolysaccharide (LPS) endotoxin shock to Ido...

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Autores principales: Yamamoto, Yasuko, Yamasuge, Wakana, Imai, Shinjiro, Kunisawa, Kazuo, Hoshi, Masato, Fujigaki, Hidetsugu, Mouri, Akihiro, Nabeshima, Toshitaka, Saito, Kuniaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206095/
https://www.ncbi.nlm.nih.gov/pubmed/30374077
http://dx.doi.org/10.1038/s41598-018-34166-4
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author Yamamoto, Yasuko
Yamasuge, Wakana
Imai, Shinjiro
Kunisawa, Kazuo
Hoshi, Masato
Fujigaki, Hidetsugu
Mouri, Akihiro
Nabeshima, Toshitaka
Saito, Kuniaki
author_facet Yamamoto, Yasuko
Yamasuge, Wakana
Imai, Shinjiro
Kunisawa, Kazuo
Hoshi, Masato
Fujigaki, Hidetsugu
Mouri, Akihiro
Nabeshima, Toshitaka
Saito, Kuniaki
author_sort Yamamoto, Yasuko
collection PubMed
description Indoleamine 2,3-dioxygenase 2 (Ido2) is a recently identified catalytic enzyme in the tryptophan-kynurenine pathway that is expressed primarily in monocytes and dendritic cells. To elucidate the biological role of Ido2 in immune function, we introduced lipopolysaccharide (LPS) endotoxin shock to Ido2 knockout (Ido2 KO) mice, which led to higher mortality than that in the wild type (WT) mice. LPS-treated Ido2 KO mice had increased production of inflammatory cytokines (including interleukin-6; IL-6) in serum and signal transducer and activator of transcription 3 (stat3) phosphorylation in the spleen. Moreover, the peritoneal macrophages of LPS-treated Ido2 KO mice produced more cytokines than did the WT mice. By contrast, the overexpression of Ido2 in the murine macrophage cell line (RAW) suppressed cytokine production and decreased stat3 expression. Finally, RAW cells overexpressing Ido2 did not alter nuclear factor κB (NF-κB) or stat1 expression, but IL-6 and stat3 expression decreased relative to the control cell line. These results reveal that Ido2 modulates IL-6/stat3 signalling and is induced by LPS, providing novel options for the treatment of immune disorders.
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spelling pubmed-62060952018-11-01 Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling Yamamoto, Yasuko Yamasuge, Wakana Imai, Shinjiro Kunisawa, Kazuo Hoshi, Masato Fujigaki, Hidetsugu Mouri, Akihiro Nabeshima, Toshitaka Saito, Kuniaki Sci Rep Article Indoleamine 2,3-dioxygenase 2 (Ido2) is a recently identified catalytic enzyme in the tryptophan-kynurenine pathway that is expressed primarily in monocytes and dendritic cells. To elucidate the biological role of Ido2 in immune function, we introduced lipopolysaccharide (LPS) endotoxin shock to Ido2 knockout (Ido2 KO) mice, which led to higher mortality than that in the wild type (WT) mice. LPS-treated Ido2 KO mice had increased production of inflammatory cytokines (including interleukin-6; IL-6) in serum and signal transducer and activator of transcription 3 (stat3) phosphorylation in the spleen. Moreover, the peritoneal macrophages of LPS-treated Ido2 KO mice produced more cytokines than did the WT mice. By contrast, the overexpression of Ido2 in the murine macrophage cell line (RAW) suppressed cytokine production and decreased stat3 expression. Finally, RAW cells overexpressing Ido2 did not alter nuclear factor κB (NF-κB) or stat1 expression, but IL-6 and stat3 expression decreased relative to the control cell line. These results reveal that Ido2 modulates IL-6/stat3 signalling and is induced by LPS, providing novel options for the treatment of immune disorders. Nature Publishing Group UK 2018-10-29 /pmc/articles/PMC6206095/ /pubmed/30374077 http://dx.doi.org/10.1038/s41598-018-34166-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yamamoto, Yasuko
Yamasuge, Wakana
Imai, Shinjiro
Kunisawa, Kazuo
Hoshi, Masato
Fujigaki, Hidetsugu
Mouri, Akihiro
Nabeshima, Toshitaka
Saito, Kuniaki
Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling
title Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling
title_full Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling
title_fullStr Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling
title_full_unstemmed Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling
title_short Lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of IL-6/stat3 signalling
title_sort lipopolysaccharide shock reveals the immune function of indoleamine 2,3-dioxygenase 2 through the regulation of il-6/stat3 signalling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206095/
https://www.ncbi.nlm.nih.gov/pubmed/30374077
http://dx.doi.org/10.1038/s41598-018-34166-4
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