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Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice

BACKGROUND: Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is increasing worldwide. Although there is currently no completely curative treatment, helminthic therapy shows certain therapeutic potential for UC. Many studies have found that Trichinella spi...

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Autores principales: Ma, Zhen-Rong, Li, Zhuo-Lin, Zhang, Ni, Lu, Bin, Li, Xuan-Wu, Huang, Ye-Hong, Nouhoum, Dibo, Liu, Xian-Shu, Xiao, Ke-Chun, Cai, Li-Ting, Xu, Shao-Rui, Yang, Xue-Xian O., Huang, Shuai-Qin, Wu, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424392/
https://www.ncbi.nlm.nih.gov/pubmed/37580819
http://dx.doi.org/10.1186/s13071-023-05857-3
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author Ma, Zhen-Rong
Li, Zhuo-Lin
Zhang, Ni
Lu, Bin
Li, Xuan-Wu
Huang, Ye-Hong
Nouhoum, Dibo
Liu, Xian-Shu
Xiao, Ke-Chun
Cai, Li-Ting
Xu, Shao-Rui
Yang, Xue-Xian O.
Huang, Shuai-Qin
Wu, Xiang
author_facet Ma, Zhen-Rong
Li, Zhuo-Lin
Zhang, Ni
Lu, Bin
Li, Xuan-Wu
Huang, Ye-Hong
Nouhoum, Dibo
Liu, Xian-Shu
Xiao, Ke-Chun
Cai, Li-Ting
Xu, Shao-Rui
Yang, Xue-Xian O.
Huang, Shuai-Qin
Wu, Xiang
author_sort Ma, Zhen-Rong
collection PubMed
description BACKGROUND: Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is increasing worldwide. Although there is currently no completely curative treatment, helminthic therapy shows certain therapeutic potential for UC. Many studies have found that Trichinella spiralis (T.s) has a protective effect on UC, but the specific mechanism is still unclear. METHODS: Balb/c mice drank dextran sulfate sodium (DSS) to induce acute colitis and then were treated with T.s. In vitro experiments, the LPS combination with ATP was used to induce the pyroptosis model, followed by intervention with crude protein from T.s (T.s cp). Additionally, the pyroptosis agonist of NSC or the pyroptosis inhibitor vx-765 was added to intervene to explore the role of pyroptosis in DSS-induced acute colitis. The degree of pyroptosis was evaluated by western blot, qPCR and IHC, etc., in vivo and in vitro. RESULTS: T.s intervention significantly inhibited NLRP3 inflammasome activation and GSDMD-mediated pyroptosis by downregulating the expression of pyroptosis-related signatures in vitro (cellular inflammatory model) and in vivo (DSS-induced UC mice model). Furthermore, blockade of GSDMD-mediated pyroptosis by the caspase-1 inhibitor vx-765 has a similar therapeutic effect on DSS-induced UC mice with T.s intervention, thus indicating that T.s intervention alleviated DSS-induced UC in mice by inhibiting GSDMD-mediated pyroptosis. CONCLUSION: This study showed that T.s could alleviate the pathological severity UC via GSDMD-mediated pyroptosis, and it provides new insight into the mechanistic study and application of helminths in treating colitis. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-023-05857-3.
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spelling pubmed-104243922023-08-15 Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice Ma, Zhen-Rong Li, Zhuo-Lin Zhang, Ni Lu, Bin Li, Xuan-Wu Huang, Ye-Hong Nouhoum, Dibo Liu, Xian-Shu Xiao, Ke-Chun Cai, Li-Ting Xu, Shao-Rui Yang, Xue-Xian O. Huang, Shuai-Qin Wu, Xiang Parasit Vectors Research BACKGROUND: Inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC), is increasing worldwide. Although there is currently no completely curative treatment, helminthic therapy shows certain therapeutic potential for UC. Many studies have found that Trichinella spiralis (T.s) has a protective effect on UC, but the specific mechanism is still unclear. METHODS: Balb/c mice drank dextran sulfate sodium (DSS) to induce acute colitis and then were treated with T.s. In vitro experiments, the LPS combination with ATP was used to induce the pyroptosis model, followed by intervention with crude protein from T.s (T.s cp). Additionally, the pyroptosis agonist of NSC or the pyroptosis inhibitor vx-765 was added to intervene to explore the role of pyroptosis in DSS-induced acute colitis. The degree of pyroptosis was evaluated by western blot, qPCR and IHC, etc., in vivo and in vitro. RESULTS: T.s intervention significantly inhibited NLRP3 inflammasome activation and GSDMD-mediated pyroptosis by downregulating the expression of pyroptosis-related signatures in vitro (cellular inflammatory model) and in vivo (DSS-induced UC mice model). Furthermore, blockade of GSDMD-mediated pyroptosis by the caspase-1 inhibitor vx-765 has a similar therapeutic effect on DSS-induced UC mice with T.s intervention, thus indicating that T.s intervention alleviated DSS-induced UC in mice by inhibiting GSDMD-mediated pyroptosis. CONCLUSION: This study showed that T.s could alleviate the pathological severity UC via GSDMD-mediated pyroptosis, and it provides new insight into the mechanistic study and application of helminths in treating colitis. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-023-05857-3. BioMed Central 2023-08-14 /pmc/articles/PMC10424392/ /pubmed/37580819 http://dx.doi.org/10.1186/s13071-023-05857-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ma, Zhen-Rong
Li, Zhuo-Lin
Zhang, Ni
Lu, Bin
Li, Xuan-Wu
Huang, Ye-Hong
Nouhoum, Dibo
Liu, Xian-Shu
Xiao, Ke-Chun
Cai, Li-Ting
Xu, Shao-Rui
Yang, Xue-Xian O.
Huang, Shuai-Qin
Wu, Xiang
Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice
title Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice
title_full Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice
title_fullStr Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice
title_full_unstemmed Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice
title_short Inhibition of GSDMD-mediated pyroptosis triggered by Trichinella spiralis intervention contributes to the alleviation of DSS-induced ulcerative colitis in mice
title_sort inhibition of gsdmd-mediated pyroptosis triggered by trichinella spiralis intervention contributes to the alleviation of dss-induced ulcerative colitis in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424392/
https://www.ncbi.nlm.nih.gov/pubmed/37580819
http://dx.doi.org/10.1186/s13071-023-05857-3
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