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SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy

Cardiopulmonary complications are major drivers of mortality caused by the SARS-CoV-2 virus. Interleukin-18, an inflammasome-induced cytokine, has emerged as a novel mediator of cardiopulmonary pathologies but its regulation via SARS-CoV-2 signaling remains unknown. Based on a screening panel, IL-18...

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Autores principales: Liang, Shuxin, Bao, Changlei, Yang, Zi, Liu, Shiyun, Sun, Yanan, Cao, Weitao, Wang, Ting, Schwantes-An, Tae-Hwi, Choy, John S., Naidu, Samisubbu, Luo, Ang, Yin, Wenguang, Black, Stephen M., Wang, Jian, Ran, Pixin, Desai, Ankit A., Tang, Haiyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998025/
https://www.ncbi.nlm.nih.gov/pubmed/36894537
http://dx.doi.org/10.1038/s41392-023-01368-w
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author Liang, Shuxin
Bao, Changlei
Yang, Zi
Liu, Shiyun
Sun, Yanan
Cao, Weitao
Wang, Ting
Schwantes-An, Tae-Hwi
Choy, John S.
Naidu, Samisubbu
Luo, Ang
Yin, Wenguang
Black, Stephen M.
Wang, Jian
Ran, Pixin
Desai, Ankit A.
Tang, Haiyang
author_facet Liang, Shuxin
Bao, Changlei
Yang, Zi
Liu, Shiyun
Sun, Yanan
Cao, Weitao
Wang, Ting
Schwantes-An, Tae-Hwi
Choy, John S.
Naidu, Samisubbu
Luo, Ang
Yin, Wenguang
Black, Stephen M.
Wang, Jian
Ran, Pixin
Desai, Ankit A.
Tang, Haiyang
author_sort Liang, Shuxin
collection PubMed
description Cardiopulmonary complications are major drivers of mortality caused by the SARS-CoV-2 virus. Interleukin-18, an inflammasome-induced cytokine, has emerged as a novel mediator of cardiopulmonary pathologies but its regulation via SARS-CoV-2 signaling remains unknown. Based on a screening panel, IL-18 was identified amongst 19 cytokines to stratify mortality and hospitalization burden in patients hospitalized with COVID-19. Supporting clinical data, administration of SARS-CoV-2 Spike 1 (S1) glycoprotein or receptor-binding domain (RBD) proteins into human angiotensin-converting enzyme 2 (hACE2) transgenic mice induced cardiac fibrosis and dysfunction associated with higher NF-κB phosphorylation (pNF-κB) and cardiopulmonary-derived IL-18 and NLRP3 expression. IL-18 inhibition via IL-18BP resulted in decreased cardiac pNF-κB and improved cardiac fibrosis and dysfunction in S1- or RBD-exposed hACE2 mice. Through in vivo and in vitro work, both S1 and RBD proteins induced NLRP3 inflammasome and IL-18 expression by inhibiting mitophagy and increasing mitochondrial reactive oxygenation species. Enhancing mitophagy prevented Spike protein-mediated IL-18 expression. Moreover, IL-18 inhibition reduced Spike protein-mediated pNF-κB and EC permeability. Overall, the link between reduced mitophagy and inflammasome activation represents a novel mechanism during COVID-19 pathogenesis and suggests IL-18 and mitophagy as potential therapeutic targets.
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spelling pubmed-99980252023-03-10 SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy Liang, Shuxin Bao, Changlei Yang, Zi Liu, Shiyun Sun, Yanan Cao, Weitao Wang, Ting Schwantes-An, Tae-Hwi Choy, John S. Naidu, Samisubbu Luo, Ang Yin, Wenguang Black, Stephen M. Wang, Jian Ran, Pixin Desai, Ankit A. Tang, Haiyang Signal Transduct Target Ther Article Cardiopulmonary complications are major drivers of mortality caused by the SARS-CoV-2 virus. Interleukin-18, an inflammasome-induced cytokine, has emerged as a novel mediator of cardiopulmonary pathologies but its regulation via SARS-CoV-2 signaling remains unknown. Based on a screening panel, IL-18 was identified amongst 19 cytokines to stratify mortality and hospitalization burden in patients hospitalized with COVID-19. Supporting clinical data, administration of SARS-CoV-2 Spike 1 (S1) glycoprotein or receptor-binding domain (RBD) proteins into human angiotensin-converting enzyme 2 (hACE2) transgenic mice induced cardiac fibrosis and dysfunction associated with higher NF-κB phosphorylation (pNF-κB) and cardiopulmonary-derived IL-18 and NLRP3 expression. IL-18 inhibition via IL-18BP resulted in decreased cardiac pNF-κB and improved cardiac fibrosis and dysfunction in S1- or RBD-exposed hACE2 mice. Through in vivo and in vitro work, both S1 and RBD proteins induced NLRP3 inflammasome and IL-18 expression by inhibiting mitophagy and increasing mitochondrial reactive oxygenation species. Enhancing mitophagy prevented Spike protein-mediated IL-18 expression. Moreover, IL-18 inhibition reduced Spike protein-mediated pNF-κB and EC permeability. Overall, the link between reduced mitophagy and inflammasome activation represents a novel mechanism during COVID-19 pathogenesis and suggests IL-18 and mitophagy as potential therapeutic targets. Nature Publishing Group UK 2023-03-09 /pmc/articles/PMC9998025/ /pubmed/36894537 http://dx.doi.org/10.1038/s41392-023-01368-w 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liang, Shuxin
Bao, Changlei
Yang, Zi
Liu, Shiyun
Sun, Yanan
Cao, Weitao
Wang, Ting
Schwantes-An, Tae-Hwi
Choy, John S.
Naidu, Samisubbu
Luo, Ang
Yin, Wenguang
Black, Stephen M.
Wang, Jian
Ran, Pixin
Desai, Ankit A.
Tang, Haiyang
SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy
title SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy
title_full SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy
title_fullStr SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy
title_full_unstemmed SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy
title_short SARS-CoV-2 spike protein induces IL-18-mediated cardiopulmonary inflammation via reduced mitophagy
title_sort sars-cov-2 spike protein induces il-18-mediated cardiopulmonary inflammation via reduced mitophagy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998025/
https://www.ncbi.nlm.nih.gov/pubmed/36894537
http://dx.doi.org/10.1038/s41392-023-01368-w
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