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Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity

Interleukin (IL)-17A, a pro-inflammatory cytokine, is a fundamental function in the onset and advancement of multiple immune diseases. To uncover the primary compounds with IL-17A inhibitory activity, a large-scale screening of the library of traditional Chinese medicine constituents and microbial s...

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Autores principales: Tang, Xin, Wang, Chuanxi, Wang, Lei, Ren, Feifei, Kuang, Runqiao, Li, Zhenhua, Han, Xue, Chen, Yiming, Chen, Guodong, Wu, Xiuqing, Liu, Jie, Yang, Hengwen, Liu, Xingzhong, Wang, Chen, Gao, Hao, Yin, Zhinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501871/
https://www.ncbi.nlm.nih.gov/pubmed/37719372
http://dx.doi.org/10.1016/j.apsb.2023.03.017
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author Tang, Xin
Wang, Chuanxi
Wang, Lei
Ren, Feifei
Kuang, Runqiao
Li, Zhenhua
Han, Xue
Chen, Yiming
Chen, Guodong
Wu, Xiuqing
Liu, Jie
Yang, Hengwen
Liu, Xingzhong
Wang, Chen
Gao, Hao
Yin, Zhinan
author_facet Tang, Xin
Wang, Chuanxi
Wang, Lei
Ren, Feifei
Kuang, Runqiao
Li, Zhenhua
Han, Xue
Chen, Yiming
Chen, Guodong
Wu, Xiuqing
Liu, Jie
Yang, Hengwen
Liu, Xingzhong
Wang, Chen
Gao, Hao
Yin, Zhinan
author_sort Tang, Xin
collection PubMed
description Interleukin (IL)-17A, a pro-inflammatory cytokine, is a fundamental function in the onset and advancement of multiple immune diseases. To uncover the primary compounds with IL-17A inhibitory activity, a large-scale screening of the library of traditional Chinese medicine constituents and microbial secondary metabolites was conducted using splenic cells from IL-17A-GFP reporter mice cultured under Th17-priming conditions. Our results indicated that some aureane-type sesquiterpene tetraketides isolated from a wetland mud-derived fungus, Myrothecium gramineum, showed remarkable IL-17A inhibitory activity. Nine new aureane-type sesquiterpene tetraketides, myrogramins A–I (1, 4–11), and two known ones (2 and 3) were isolated and identified from the strain. Compounds 1, 3, 4, 10, and 11 exhibited significant IL-17A inhibitory activity. Among them, compound 3, with a high fermentation yield dose-dependently inhibited the generation of IL-17A and suppressed glycolysis in splenic cells under Th17-priming conditions. Strikingly, compound 3 suppressed immunopathology in both IL-17A-mediated animal models of experimental autoimmune encephalomyelitis and pulmonary hypertension. Our results revealed that aureane-type sesquiterpene tetraketides are a novel class of immunomodulators with IL-17A inhibitory activity, and hold great promise applications in treating IL-17A-mediated immune diseases.
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spelling pubmed-105018712023-09-16 Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity Tang, Xin Wang, Chuanxi Wang, Lei Ren, Feifei Kuang, Runqiao Li, Zhenhua Han, Xue Chen, Yiming Chen, Guodong Wu, Xiuqing Liu, Jie Yang, Hengwen Liu, Xingzhong Wang, Chen Gao, Hao Yin, Zhinan Acta Pharm Sin B Original Article Interleukin (IL)-17A, a pro-inflammatory cytokine, is a fundamental function in the onset and advancement of multiple immune diseases. To uncover the primary compounds with IL-17A inhibitory activity, a large-scale screening of the library of traditional Chinese medicine constituents and microbial secondary metabolites was conducted using splenic cells from IL-17A-GFP reporter mice cultured under Th17-priming conditions. Our results indicated that some aureane-type sesquiterpene tetraketides isolated from a wetland mud-derived fungus, Myrothecium gramineum, showed remarkable IL-17A inhibitory activity. Nine new aureane-type sesquiterpene tetraketides, myrogramins A–I (1, 4–11), and two known ones (2 and 3) were isolated and identified from the strain. Compounds 1, 3, 4, 10, and 11 exhibited significant IL-17A inhibitory activity. Among them, compound 3, with a high fermentation yield dose-dependently inhibited the generation of IL-17A and suppressed glycolysis in splenic cells under Th17-priming conditions. Strikingly, compound 3 suppressed immunopathology in both IL-17A-mediated animal models of experimental autoimmune encephalomyelitis and pulmonary hypertension. Our results revealed that aureane-type sesquiterpene tetraketides are a novel class of immunomodulators with IL-17A inhibitory activity, and hold great promise applications in treating IL-17A-mediated immune diseases. Elsevier 2023-09 2023-03-21 /pmc/articles/PMC10501871/ /pubmed/37719372 http://dx.doi.org/10.1016/j.apsb.2023.03.017 Text en © 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://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 Original Article
Tang, Xin
Wang, Chuanxi
Wang, Lei
Ren, Feifei
Kuang, Runqiao
Li, Zhenhua
Han, Xue
Chen, Yiming
Chen, Guodong
Wu, Xiuqing
Liu, Jie
Yang, Hengwen
Liu, Xingzhong
Wang, Chen
Gao, Hao
Yin, Zhinan
Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
title Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
title_full Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
title_fullStr Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
title_full_unstemmed Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
title_short Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
title_sort aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17a inhibitory activity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501871/
https://www.ncbi.nlm.nih.gov/pubmed/37719372
http://dx.doi.org/10.1016/j.apsb.2023.03.017
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