Cargando…

Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages

The nucleotide-binding domain, leucine-rich-repeat containing family, pyrin domain-containing 3 (NLRP3) inflammasome is essential in inflammation and inflammatory disorders. Phosphorylation at various sites on NLRP3 differentially regulates inflammasome activation. The Ser725 phosphorylation site on...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhu, Kaixiang, Jin, Xuexiao, Chi, Zhexu, Chen, Sheng, Wu, Songquan, Sloan, Richard D., Lin, Xuai, Neculai, Dante, Wang, Di, Hu, Hu, Lu, Linrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414466/
https://www.ncbi.nlm.nih.gov/pubmed/34480147
http://dx.doi.org/10.1038/s41423-021-00761-1
_version_ 1783747787179950080
author Zhu, Kaixiang
Jin, Xuexiao
Chi, Zhexu
Chen, Sheng
Wu, Songquan
Sloan, Richard D.
Lin, Xuai
Neculai, Dante
Wang, Di
Hu, Hu
Lu, Linrong
author_facet Zhu, Kaixiang
Jin, Xuexiao
Chi, Zhexu
Chen, Sheng
Wu, Songquan
Sloan, Richard D.
Lin, Xuai
Neculai, Dante
Wang, Di
Hu, Hu
Lu, Linrong
author_sort Zhu, Kaixiang
collection PubMed
description The nucleotide-binding domain, leucine-rich-repeat containing family, pyrin domain-containing 3 (NLRP3) inflammasome is essential in inflammation and inflammatory disorders. Phosphorylation at various sites on NLRP3 differentially regulates inflammasome activation. The Ser725 phosphorylation site on NLRP3 is depicted in multiple inflammasome activation scenarios, but the importance and regulation of this site has not been clarified. The present study revealed that the phosphorylation of Ser725 was an essential step for the priming of the NLRP3 inflammasome in macrophages. We also showed that Ser725 was directly phosphorylated by misshapen (Msn)/NIK-related kinase 1 (MINK1), depending on the direct interaction between MINK1 and the NLRP3 LRR domain. MINK1 deficiency reduced NLRP3 activation and suppressed inflammatory responses in mouse models of acute sepsis and peritonitis. Reactive oxygen species (ROS) upregulated the kinase activity of MINK1 and subsequently promoted inflammasome priming via NLRP3 Ser725 phosphorylation. Eliminating ROS suppressed NLRP3 activation and reduced sepsis and peritonitis symptoms in a MINK1-dependent manner. Altogether, our study reveals a direct regulation of the NLRP3 inflammasome by Msn family kinase MINK1 and suggests that modulation of MINK1 activity is a potential intervention strategy for inflammasome-related diseases.
format Online
Article
Text
id pubmed-8414466
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-84144662021-09-03 Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages Zhu, Kaixiang Jin, Xuexiao Chi, Zhexu Chen, Sheng Wu, Songquan Sloan, Richard D. Lin, Xuai Neculai, Dante Wang, Di Hu, Hu Lu, Linrong Cell Mol Immunol Article The nucleotide-binding domain, leucine-rich-repeat containing family, pyrin domain-containing 3 (NLRP3) inflammasome is essential in inflammation and inflammatory disorders. Phosphorylation at various sites on NLRP3 differentially regulates inflammasome activation. The Ser725 phosphorylation site on NLRP3 is depicted in multiple inflammasome activation scenarios, but the importance and regulation of this site has not been clarified. The present study revealed that the phosphorylation of Ser725 was an essential step for the priming of the NLRP3 inflammasome in macrophages. We also showed that Ser725 was directly phosphorylated by misshapen (Msn)/NIK-related kinase 1 (MINK1), depending on the direct interaction between MINK1 and the NLRP3 LRR domain. MINK1 deficiency reduced NLRP3 activation and suppressed inflammatory responses in mouse models of acute sepsis and peritonitis. Reactive oxygen species (ROS) upregulated the kinase activity of MINK1 and subsequently promoted inflammasome priming via NLRP3 Ser725 phosphorylation. Eliminating ROS suppressed NLRP3 activation and reduced sepsis and peritonitis symptoms in a MINK1-dependent manner. Altogether, our study reveals a direct regulation of the NLRP3 inflammasome by Msn family kinase MINK1 and suggests that modulation of MINK1 activity is a potential intervention strategy for inflammasome-related diseases. Nature Publishing Group UK 2021-09-03 2021-10 /pmc/articles/PMC8414466/ /pubmed/34480147 http://dx.doi.org/10.1038/s41423-021-00761-1 Text en © The Author(s), under exclusive licence to CSI and USTC 2021
spellingShingle Article
Zhu, Kaixiang
Jin, Xuexiao
Chi, Zhexu
Chen, Sheng
Wu, Songquan
Sloan, Richard D.
Lin, Xuai
Neculai, Dante
Wang, Di
Hu, Hu
Lu, Linrong
Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages
title Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages
title_full Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages
title_fullStr Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages
title_full_unstemmed Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages
title_short Priming of NLRP3 inflammasome activation by Msn kinase MINK1 in macrophages
title_sort priming of nlrp3 inflammasome activation by msn kinase mink1 in macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414466/
https://www.ncbi.nlm.nih.gov/pubmed/34480147
http://dx.doi.org/10.1038/s41423-021-00761-1
work_keys_str_mv AT zhukaixiang primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT jinxuexiao primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT chizhexu primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT chensheng primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT wusongquan primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT sloanrichardd primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT linxuai primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT neculaidante primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT wangdi primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT huhu primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages
AT lulinrong primingofnlrp3inflammasomeactivationbymsnkinasemink1inmacrophages