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SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses
BACKGROUND: T lymphocytes play an important role in contact hypersensitivity. This study aims to explore the immunosuppressive activity of SBF-1, an analog of saponin OSW-1, against T lymphocytes in vitro and in vivo. METHODS: Proliferation of T lymphocytes from lymph nodes of mice was determined by...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925477/ https://www.ncbi.nlm.nih.gov/pubmed/31864413 http://dx.doi.org/10.1186/s40360-019-0377-8 |
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author | Chen, Wei Fang, Xianying Gao, Yuan Shi, Ke Sun, Lijun Yu, Biao Luo, Qiong Xu, Qiang |
author_facet | Chen, Wei Fang, Xianying Gao, Yuan Shi, Ke Sun, Lijun Yu, Biao Luo, Qiong Xu, Qiang |
author_sort | Chen, Wei |
collection | PubMed |
description | BACKGROUND: T lymphocytes play an important role in contact hypersensitivity. This study aims to explore the immunosuppressive activity of SBF-1, an analog of saponin OSW-1, against T lymphocytes in vitro and in vivo. METHODS: Proliferation of T lymphocytes from lymph nodes of mice was determined by MTT assay. Flow cytometry analysis was performed to assess T cell activation and apoptosis. Levels of cytokines were determined by PCR and ELISA. BALB/c mice were sensitized and challenged with picryl chloride and thickness of left and right ears were measured. RESULTS: SBF-1 effectively inhibited T lymphocytes proliferation induced by concanavalin A (Con A) or anti-CD3 plus anti-CD28 at a very low dose (10 nM) but exhibited little toxicity in non-activated T lymphocytes at concentrations up to 10 μM. In addition, SBF-1 inhibited the expression of CD25 and CD69, as well as he phosphorylation of AKT in Con A-activated T cells. SBF-1 also induced apoptosis of activated T cells. In addition, SBF-1 also downregulated the induction of the T cell cytokines, IL-2 and IFN-γ in a dose-dependent manner. Furthermore, SBF-1 significantly suppressed ear swelling and inflammation in a mouse model of picryl chloride-induced contact hypersensitivity. CONCLUSIONS: Our findings suggest that SBF-1 has an unique immunosuppressive activity both in vitro and in vivo mainly through inhibiting T cell proliferation and activation. Its mechanism appears to be related to the blockage of AKT signaling pathway. |
format | Online Article Text |
id | pubmed-6925477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69254772019-12-30 SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses Chen, Wei Fang, Xianying Gao, Yuan Shi, Ke Sun, Lijun Yu, Biao Luo, Qiong Xu, Qiang BMC Pharmacol Toxicol Research Article BACKGROUND: T lymphocytes play an important role in contact hypersensitivity. This study aims to explore the immunosuppressive activity of SBF-1, an analog of saponin OSW-1, against T lymphocytes in vitro and in vivo. METHODS: Proliferation of T lymphocytes from lymph nodes of mice was determined by MTT assay. Flow cytometry analysis was performed to assess T cell activation and apoptosis. Levels of cytokines were determined by PCR and ELISA. BALB/c mice were sensitized and challenged with picryl chloride and thickness of left and right ears were measured. RESULTS: SBF-1 effectively inhibited T lymphocytes proliferation induced by concanavalin A (Con A) or anti-CD3 plus anti-CD28 at a very low dose (10 nM) but exhibited little toxicity in non-activated T lymphocytes at concentrations up to 10 μM. In addition, SBF-1 inhibited the expression of CD25 and CD69, as well as he phosphorylation of AKT in Con A-activated T cells. SBF-1 also induced apoptosis of activated T cells. In addition, SBF-1 also downregulated the induction of the T cell cytokines, IL-2 and IFN-γ in a dose-dependent manner. Furthermore, SBF-1 significantly suppressed ear swelling and inflammation in a mouse model of picryl chloride-induced contact hypersensitivity. CONCLUSIONS: Our findings suggest that SBF-1 has an unique immunosuppressive activity both in vitro and in vivo mainly through inhibiting T cell proliferation and activation. Its mechanism appears to be related to the blockage of AKT signaling pathway. BioMed Central 2019-12-21 /pmc/articles/PMC6925477/ /pubmed/31864413 http://dx.doi.org/10.1186/s40360-019-0377-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chen, Wei Fang, Xianying Gao, Yuan Shi, Ke Sun, Lijun Yu, Biao Luo, Qiong Xu, Qiang SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses |
title | SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses |
title_full | SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses |
title_fullStr | SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses |
title_full_unstemmed | SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses |
title_short | SBF-1 inhibits contact hypersensitivity in mice through down-regulation of T-cell-mediated responses |
title_sort | sbf-1 inhibits contact hypersensitivity in mice through down-regulation of t-cell-mediated responses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925477/ https://www.ncbi.nlm.nih.gov/pubmed/31864413 http://dx.doi.org/10.1186/s40360-019-0377-8 |
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