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Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells

d-Glucosamine (GlcNH(2)) and several of its derivatives are known to possess immunosuppressive activities in various immune cell lines. The novel GlcNH(2)-containing oligosaccharide Galα1-6GlcNH(2) (designated melibiosamine; MelNH(2)) is expected to be immunosuppressive also. In Jurkat cells (immort...

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Autores principales: Fujita, Kazuki, Tanaka, Susumu, Iizumi, Kyoichi, Akiyama, Shuri, Uchida, Kaoru, Ogata, Makoto, Aoki, Daichi, Hosomi, Osamu, Kubohara, Yuzuru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580327/
https://www.ncbi.nlm.nih.gov/pubmed/31431927
http://dx.doi.org/10.1016/j.bbrep.2019.100658
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author Fujita, Kazuki
Tanaka, Susumu
Iizumi, Kyoichi
Akiyama, Shuri
Uchida, Kaoru
Ogata, Makoto
Aoki, Daichi
Hosomi, Osamu
Kubohara, Yuzuru
author_facet Fujita, Kazuki
Tanaka, Susumu
Iizumi, Kyoichi
Akiyama, Shuri
Uchida, Kaoru
Ogata, Makoto
Aoki, Daichi
Hosomi, Osamu
Kubohara, Yuzuru
author_sort Fujita, Kazuki
collection PubMed
description d-Glucosamine (GlcNH(2)) and several of its derivatives are known to possess immunosuppressive activities in various immune cell lines. The novel GlcNH(2)-containing oligosaccharide Galα1-6GlcNH(2) (designated melibiosamine; MelNH(2)) is expected to be immunosuppressive also. In Jurkat cells (immortalized human T lymphocytes), interleukin 2 (IL-2) production (an index of the T-cell immune response) can be induced by stimulation with a mitogen, such as concanavalin A. Here, we compared the effects of GlcNH(2) and MelNH(2) on concanavalin A-induced IL-2 production (CIIP) in Jurkat cells and found that GlcNH(2) and MelNH(2) at millimolar levels both significantly suppressed CIIP without affecting cell viability. When we examined the effects of GlcNH(2) and MelNH(2) on the activation of the three transcription factors required for CIIP—NFAT (nuclear factor of activated T-cells), NFκB (nuclear factor kappa-light-chain-enhancer of activated B cells), and AP-1 (activator protein 1)—we found that GlcNH(2) and MelNH(2) both suppressed CIIP by inhibiting the activation of NFAT and NFκB, but, unlike GlcNH(2), MelNH(2) also promoted the activation of AP-1. These results suggest that MelNH(2) may be a potentially useful lead compound for development as an immunosuppressive or anti-inflammatory drug.
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spelling pubmed-65803272019-08-20 Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells Fujita, Kazuki Tanaka, Susumu Iizumi, Kyoichi Akiyama, Shuri Uchida, Kaoru Ogata, Makoto Aoki, Daichi Hosomi, Osamu Kubohara, Yuzuru Biochem Biophys Rep Research Article d-Glucosamine (GlcNH(2)) and several of its derivatives are known to possess immunosuppressive activities in various immune cell lines. The novel GlcNH(2)-containing oligosaccharide Galα1-6GlcNH(2) (designated melibiosamine; MelNH(2)) is expected to be immunosuppressive also. In Jurkat cells (immortalized human T lymphocytes), interleukin 2 (IL-2) production (an index of the T-cell immune response) can be induced by stimulation with a mitogen, such as concanavalin A. Here, we compared the effects of GlcNH(2) and MelNH(2) on concanavalin A-induced IL-2 production (CIIP) in Jurkat cells and found that GlcNH(2) and MelNH(2) at millimolar levels both significantly suppressed CIIP without affecting cell viability. When we examined the effects of GlcNH(2) and MelNH(2) on the activation of the three transcription factors required for CIIP—NFAT (nuclear factor of activated T-cells), NFκB (nuclear factor kappa-light-chain-enhancer of activated B cells), and AP-1 (activator protein 1)—we found that GlcNH(2) and MelNH(2) both suppressed CIIP by inhibiting the activation of NFAT and NFκB, but, unlike GlcNH(2), MelNH(2) also promoted the activation of AP-1. These results suggest that MelNH(2) may be a potentially useful lead compound for development as an immunosuppressive or anti-inflammatory drug. Elsevier 2019-06-14 /pmc/articles/PMC6580327/ /pubmed/31431927 http://dx.doi.org/10.1016/j.bbrep.2019.100658 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Fujita, Kazuki
Tanaka, Susumu
Iizumi, Kyoichi
Akiyama, Shuri
Uchida, Kaoru
Ogata, Makoto
Aoki, Daichi
Hosomi, Osamu
Kubohara, Yuzuru
Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells
title Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells
title_full Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells
title_fullStr Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells
title_full_unstemmed Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells
title_short Melibiosamine, a novel oligosaccharide, suppresses mitogen-induced IL-2 production via inactivation of NFAT and NFκB in Jurkat cells
title_sort melibiosamine, a novel oligosaccharide, suppresses mitogen-induced il-2 production via inactivation of nfat and nfκb in jurkat cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580327/
https://www.ncbi.nlm.nih.gov/pubmed/31431927
http://dx.doi.org/10.1016/j.bbrep.2019.100658
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