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Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression
BACKGROUND: We previously reported that tacrolimus (Tac) does not decrease T helper 17 cells (Th17) response in kidney transplantation. In this study, we evaluated whether Resveratrol (Resv) has immunosuppressive effects by decreasing Th17 responses in Tac-based immunosuppression. METHODS: We invest...
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/PMC6399827/ https://www.ncbi.nlm.nih.gov/pubmed/30832648 http://dx.doi.org/10.1186/s12906-019-2464-1 |
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author | Doh, Kyoung Chan Kim, Bo-Mi Kim, Kyoung Woon Chung, Byung Ha Yang, Chul Woo |
author_facet | Doh, Kyoung Chan Kim, Bo-Mi Kim, Kyoung Woon Chung, Byung Ha Yang, Chul Woo |
author_sort | Doh, Kyoung Chan |
collection | PubMed |
description | BACKGROUND: We previously reported that tacrolimus (Tac) does not decrease T helper 17 cells (Th17) response in kidney transplantation. In this study, we evaluated whether Resveratrol (Resv) has immunosuppressive effects by decreasing Th17 responses in Tac-based immunosuppression. METHODS: We investigated the effects of Resv under Tac-treatment conditions, on CD4(+) T cell differentiation to Th17 cells in peripheral blood mononuclear cells (PBMCs), and proliferation of CD4(+) T cells co-cultured with human renal proximal tubular epithelial cells (HRPTEpiCs). The effects of Resv on Th17 cells were tested in the murine skin transplant model. RESULTS: In PBMCs, Tac did not but combination of Tac and Resv further suppressed Th17 immune response. In the co-culture study, combination of Resv to Tac significantly decreased HRPTEpiC-induced T cell proliferation compared to Tac alone. Resv treatment in the Jurkat cell induced the expression of AMP-activated protein kinase and suppressed the expression of mammalian target of rapamycin (mTOR), suggesting blocking Th17 pathway by Resv. In the murine skin transplant model, combination of Resv to Tac significantly prolonged skin graft survival accompanied by the suppression of Th17 cells, compared to either the Tac-alone or control groups. CONCLUSION: The results of our study suggest that Resv provides additional immunosuppressive effects to Tac by suppressing effector CD4(+) T cells, especially Th17 cells, in the transplantation setting. |
format | Online Article Text |
id | pubmed-6399827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63998272019-03-13 Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression Doh, Kyoung Chan Kim, Bo-Mi Kim, Kyoung Woon Chung, Byung Ha Yang, Chul Woo BMC Complement Altern Med Research Article BACKGROUND: We previously reported that tacrolimus (Tac) does not decrease T helper 17 cells (Th17) response in kidney transplantation. In this study, we evaluated whether Resveratrol (Resv) has immunosuppressive effects by decreasing Th17 responses in Tac-based immunosuppression. METHODS: We investigated the effects of Resv under Tac-treatment conditions, on CD4(+) T cell differentiation to Th17 cells in peripheral blood mononuclear cells (PBMCs), and proliferation of CD4(+) T cells co-cultured with human renal proximal tubular epithelial cells (HRPTEpiCs). The effects of Resv on Th17 cells were tested in the murine skin transplant model. RESULTS: In PBMCs, Tac did not but combination of Tac and Resv further suppressed Th17 immune response. In the co-culture study, combination of Resv to Tac significantly decreased HRPTEpiC-induced T cell proliferation compared to Tac alone. Resv treatment in the Jurkat cell induced the expression of AMP-activated protein kinase and suppressed the expression of mammalian target of rapamycin (mTOR), suggesting blocking Th17 pathway by Resv. In the murine skin transplant model, combination of Resv to Tac significantly prolonged skin graft survival accompanied by the suppression of Th17 cells, compared to either the Tac-alone or control groups. CONCLUSION: The results of our study suggest that Resv provides additional immunosuppressive effects to Tac by suppressing effector CD4(+) T cells, especially Th17 cells, in the transplantation setting. BioMed Central 2019-03-04 /pmc/articles/PMC6399827/ /pubmed/30832648 http://dx.doi.org/10.1186/s12906-019-2464-1 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 Doh, Kyoung Chan Kim, Bo-Mi Kim, Kyoung Woon Chung, Byung Ha Yang, Chul Woo Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression |
title | Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression |
title_full | Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression |
title_fullStr | Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression |
title_full_unstemmed | Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression |
title_short | Effects of resveratrol on Th17 cell-related immune responses under tacrolimus-based immunosuppression |
title_sort | effects of resveratrol on th17 cell-related immune responses under tacrolimus-based immunosuppression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399827/ https://www.ncbi.nlm.nih.gov/pubmed/30832648 http://dx.doi.org/10.1186/s12906-019-2464-1 |
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