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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6580327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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