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Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis

Liver cirrhosis represents a type of end-stage liver disease with few effective therapies, which was characterized by damaged functional liver tissue due to long-term inflammation. Gasdermin D (GSDMD)-executed programmed necrosis is reported to be involved in inflammation. However, the role of GSDMD...

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Autores principales: Chen, Peng, Zhou, Yi-kun, Han, Chun-shan, Chen, Liu-jing, Wang, Yi-ming, Zhuang, Zi-meng, Lin, Shuai, Zhou, Yan-heng, Jiang, Jiu-hui, Yang, Rui-li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133376/
https://www.ncbi.nlm.nih.gov/pubmed/35634294
http://dx.doi.org/10.3389/fimmu.2022.860225
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author Chen, Peng
Zhou, Yi-kun
Han, Chun-shan
Chen, Liu-jing
Wang, Yi-ming
Zhuang, Zi-meng
Lin, Shuai
Zhou, Yan-heng
Jiang, Jiu-hui
Yang, Rui-li
author_facet Chen, Peng
Zhou, Yi-kun
Han, Chun-shan
Chen, Liu-jing
Wang, Yi-ming
Zhuang, Zi-meng
Lin, Shuai
Zhou, Yan-heng
Jiang, Jiu-hui
Yang, Rui-li
author_sort Chen, Peng
collection PubMed
description Liver cirrhosis represents a type of end-stage liver disease with few effective therapies, which was characterized by damaged functional liver tissue due to long-term inflammation. Gasdermin D (GSDMD)-executed programmed necrosis is reported to be involved in inflammation. However, the role of GSDMD in liver cirrhosis remains unclear. In this study, we used a CCl(4)-induced cirrhosis model and found stem cells from human exfoliated deciduous teeth (SHED) infusion showed profound therapeutic effects for liver cirrhosis. Mechanistically, NLRP3 inflammasome-activated GSDMD and its pyroptosis were upregulated in liver cirrhosis, while SHED infusion could suppress the expression of GSDMD and Caspase-1, resulting in reduced hepatocyte pyroptosis and inflammatory cytokine IL-1β release. Consistently, SHED could inhibit the elevated expression of NLRP3, GSDMD and Caspase-1 induced by CCl(4) treatment in vitro co-culture system, which was mediated by decreasing reactive oxygen species (ROS) generation. Moreover, the pyroptosis inhibitor disulfiram showed similar therapeutic effects for liver cirrhosis as SHED. In conclusion, SHED alleviates CCl(4)-induced liver cirrhosis via inhibition of hepatocytes pyroptosis. Our findings could provide a potential treatment strategy and novel target for liver cirrhosis.
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spelling pubmed-91333762022-05-27 Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis Chen, Peng Zhou, Yi-kun Han, Chun-shan Chen, Liu-jing Wang, Yi-ming Zhuang, Zi-meng Lin, Shuai Zhou, Yan-heng Jiang, Jiu-hui Yang, Rui-li Front Immunol Immunology Liver cirrhosis represents a type of end-stage liver disease with few effective therapies, which was characterized by damaged functional liver tissue due to long-term inflammation. Gasdermin D (GSDMD)-executed programmed necrosis is reported to be involved in inflammation. However, the role of GSDMD in liver cirrhosis remains unclear. In this study, we used a CCl(4)-induced cirrhosis model and found stem cells from human exfoliated deciduous teeth (SHED) infusion showed profound therapeutic effects for liver cirrhosis. Mechanistically, NLRP3 inflammasome-activated GSDMD and its pyroptosis were upregulated in liver cirrhosis, while SHED infusion could suppress the expression of GSDMD and Caspase-1, resulting in reduced hepatocyte pyroptosis and inflammatory cytokine IL-1β release. Consistently, SHED could inhibit the elevated expression of NLRP3, GSDMD and Caspase-1 induced by CCl(4) treatment in vitro co-culture system, which was mediated by decreasing reactive oxygen species (ROS) generation. Moreover, the pyroptosis inhibitor disulfiram showed similar therapeutic effects for liver cirrhosis as SHED. In conclusion, SHED alleviates CCl(4)-induced liver cirrhosis via inhibition of hepatocytes pyroptosis. Our findings could provide a potential treatment strategy and novel target for liver cirrhosis. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9133376/ /pubmed/35634294 http://dx.doi.org/10.3389/fimmu.2022.860225 Text en Copyright © 2022 Chen, Zhou, Han, Chen, Wang, Zhuang, Lin, Zhou, Jiang and Yang 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 Immunology
Chen, Peng
Zhou, Yi-kun
Han, Chun-shan
Chen, Liu-jing
Wang, Yi-ming
Zhuang, Zi-meng
Lin, Shuai
Zhou, Yan-heng
Jiang, Jiu-hui
Yang, Rui-li
Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis
title Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis
title_full Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis
title_fullStr Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis
title_full_unstemmed Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis
title_short Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis via Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis
title_sort stem cells from human exfoliated deciduous teeth alleviate liver cirrhosis via inhibition of gasdermin d-executed hepatocyte pyroptosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133376/
https://www.ncbi.nlm.nih.gov/pubmed/35634294
http://dx.doi.org/10.3389/fimmu.2022.860225
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