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Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels
Loureirin B (LrB) is a constituent extracted from traditional Chinese medicine Resina Draconis. It has broad biological functions and an impressive immunosuppressive effect that has been supported by numerous studies. However, the molecular mechanisms underlying Loureirin B-induced immune suppressio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268022/ https://www.ncbi.nlm.nih.gov/pubmed/34248635 http://dx.doi.org/10.3389/fphar.2021.685092 |
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author | Shi, Shujuan Zhao, Qianru Ke, Caihua Long, Siru Zhang, Feng Zhang, Xu Li, Yi Liu, Xinqiao Hu, Hongzhen Yin, Shijin |
author_facet | Shi, Shujuan Zhao, Qianru Ke, Caihua Long, Siru Zhang, Feng Zhang, Xu Li, Yi Liu, Xinqiao Hu, Hongzhen Yin, Shijin |
author_sort | Shi, Shujuan |
collection | PubMed |
description | Loureirin B (LrB) is a constituent extracted from traditional Chinese medicine Resina Draconis. It has broad biological functions and an impressive immunosuppressive effect that has been supported by numerous studies. However, the molecular mechanisms underlying Loureirin B-induced immune suppression are not fully understood. We previously reported that Loureirin B inhibited K(V)1.3 channel, calcium ion (Ca(2+)) influx, and interleukin-2 (IL-2) secretion in Jurkat T cells. In this study, we applied CRISPR/Cas9 to edit K(V)1.3 coding gene KCNA3 and successfully generated a K(V)1.3 knockout (KO) cell model to determine whether K(V)1.3 KO was sufficient to block the Loureirin B-induced immunosuppressive effect. Surprisingly, we showed that Loureirin B could still inhibit Ca(2+) influx and IL-2 secretion in the Jurkat T cells in the absence of K(V)1.3 although KO K(V)1.3 reduced about 50% of Ca(2+) influx and 90% IL-2 secretion compared with that in the wild type cells. Further experiments showed that Loureirin B directly inhibited STIM1/Orai1 channel in a dose-dependent manner. Our results suggest that Loureirin B inhibits Ca(2+) influx and IL-2 secretion in Jurkat T cells by inhibiting both K(V)1.3 and STIM1/Orai1 channels. These studies also revealed an additional molecular target for Loureirin B-induced immunosuppressive effect, which makes it a promising leading compound for treating autoimmune diseases. |
format | Online Article Text |
id | pubmed-8268022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82680222021-07-10 Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels Shi, Shujuan Zhao, Qianru Ke, Caihua Long, Siru Zhang, Feng Zhang, Xu Li, Yi Liu, Xinqiao Hu, Hongzhen Yin, Shijin Front Pharmacol Pharmacology Loureirin B (LrB) is a constituent extracted from traditional Chinese medicine Resina Draconis. It has broad biological functions and an impressive immunosuppressive effect that has been supported by numerous studies. However, the molecular mechanisms underlying Loureirin B-induced immune suppression are not fully understood. We previously reported that Loureirin B inhibited K(V)1.3 channel, calcium ion (Ca(2+)) influx, and interleukin-2 (IL-2) secretion in Jurkat T cells. In this study, we applied CRISPR/Cas9 to edit K(V)1.3 coding gene KCNA3 and successfully generated a K(V)1.3 knockout (KO) cell model to determine whether K(V)1.3 KO was sufficient to block the Loureirin B-induced immunosuppressive effect. Surprisingly, we showed that Loureirin B could still inhibit Ca(2+) influx and IL-2 secretion in the Jurkat T cells in the absence of K(V)1.3 although KO K(V)1.3 reduced about 50% of Ca(2+) influx and 90% IL-2 secretion compared with that in the wild type cells. Further experiments showed that Loureirin B directly inhibited STIM1/Orai1 channel in a dose-dependent manner. Our results suggest that Loureirin B inhibits Ca(2+) influx and IL-2 secretion in Jurkat T cells by inhibiting both K(V)1.3 and STIM1/Orai1 channels. These studies also revealed an additional molecular target for Loureirin B-induced immunosuppressive effect, which makes it a promising leading compound for treating autoimmune diseases. Frontiers Media S.A. 2021-06-25 /pmc/articles/PMC8268022/ /pubmed/34248635 http://dx.doi.org/10.3389/fphar.2021.685092 Text en Copyright © 2021 Shi, Zhao, Ke, Long, Zhang, Zhang, Li, Liu, Hu and Yin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Shi, Shujuan Zhao, Qianru Ke, Caihua Long, Siru Zhang, Feng Zhang, Xu Li, Yi Liu, Xinqiao Hu, Hongzhen Yin, Shijin Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels |
title | Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels |
title_full | Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels |
title_fullStr | Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels |
title_full_unstemmed | Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels |
title_short | Loureirin B Exerts its Immunosuppressive Effects by Inhibiting STIM1/Orai1 and K(V)1.3 Channels |
title_sort | loureirin b exerts its immunosuppressive effects by inhibiting stim1/orai1 and k(v)1.3 channels |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268022/ https://www.ncbi.nlm.nih.gov/pubmed/34248635 http://dx.doi.org/10.3389/fphar.2021.685092 |
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