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The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation

Pasteurella multocida is a zoonotic pathogen causing respiratory infection in different animal species such as cattle, sheep, pigs, chickens and humans. Inflammasome is a complex assembled by multiple proteins in the cytoplasm and plays an important role in the host defense against microbial infecti...

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Autores principales: Wang, Yu, Zeng, Zheng, Ran, Jinrong, Peng, Lianci, Wu, Xingping, Ye, Chao, Dong, Chunxia, Peng, Yuanyi, Fang, Rendong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957907/
https://www.ncbi.nlm.nih.gov/pubmed/35350616
http://dx.doi.org/10.3389/fmicb.2022.849482
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author Wang, Yu
Zeng, Zheng
Ran, Jinrong
Peng, Lianci
Wu, Xingping
Ye, Chao
Dong, Chunxia
Peng, Yuanyi
Fang, Rendong
author_facet Wang, Yu
Zeng, Zheng
Ran, Jinrong
Peng, Lianci
Wu, Xingping
Ye, Chao
Dong, Chunxia
Peng, Yuanyi
Fang, Rendong
author_sort Wang, Yu
collection PubMed
description Pasteurella multocida is a zoonotic pathogen causing respiratory infection in different animal species such as cattle, sheep, pigs, chickens and humans. Inflammasome is a complex assembled by multiple proteins in the cytoplasm and plays an important role in the host defense against microbial infection. Bovine Pasteurella multocida type A (PmCQ2) infection induces NLRP3 inflammasome activation and IL-1β secretion, but the mechanism of PmCQ2-induced activation of NLRP3 inflammasome is still unknown. Therefore, the underlying mechanism was investigated in this study. The results showed that potassium efflux mediated PmCQ2-induced IL-1β secretion and blocking potassium efflux attenuated PmCQ2-induced caspase-1 activation and ASC oligomerization. Furthermore, NIMA-related kinase 7 (Nek7) was also involved in PmCQ2-induced caspase-1 activation and IL-1β secretion. In addition, PmCQ2 infection promoted Nek7-NLRP3 interaction, which is dependent on potassium efflux. In conclusion, our results indicate the critical role of potassium efflux and Nek7 in Pasteurella multocida-induced NLRP3 inflammasome activation, which provides useful information about Pasteurella multocida-induced host immune response.
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spelling pubmed-89579072022-03-28 The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation Wang, Yu Zeng, Zheng Ran, Jinrong Peng, Lianci Wu, Xingping Ye, Chao Dong, Chunxia Peng, Yuanyi Fang, Rendong Front Microbiol Microbiology Pasteurella multocida is a zoonotic pathogen causing respiratory infection in different animal species such as cattle, sheep, pigs, chickens and humans. Inflammasome is a complex assembled by multiple proteins in the cytoplasm and plays an important role in the host defense against microbial infection. Bovine Pasteurella multocida type A (PmCQ2) infection induces NLRP3 inflammasome activation and IL-1β secretion, but the mechanism of PmCQ2-induced activation of NLRP3 inflammasome is still unknown. Therefore, the underlying mechanism was investigated in this study. The results showed that potassium efflux mediated PmCQ2-induced IL-1β secretion and blocking potassium efflux attenuated PmCQ2-induced caspase-1 activation and ASC oligomerization. Furthermore, NIMA-related kinase 7 (Nek7) was also involved in PmCQ2-induced caspase-1 activation and IL-1β secretion. In addition, PmCQ2 infection promoted Nek7-NLRP3 interaction, which is dependent on potassium efflux. In conclusion, our results indicate the critical role of potassium efflux and Nek7 in Pasteurella multocida-induced NLRP3 inflammasome activation, which provides useful information about Pasteurella multocida-induced host immune response. Frontiers Media S.A. 2022-03-08 /pmc/articles/PMC8957907/ /pubmed/35350616 http://dx.doi.org/10.3389/fmicb.2022.849482 Text en Copyright © 2022 Wang, Zeng, Ran, Peng, Wu, Ye, Dong, Peng and Fang. 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 Microbiology
Wang, Yu
Zeng, Zheng
Ran, Jinrong
Peng, Lianci
Wu, Xingping
Ye, Chao
Dong, Chunxia
Peng, Yuanyi
Fang, Rendong
The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation
title The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation
title_full The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation
title_fullStr The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation
title_full_unstemmed The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation
title_short The Critical Role of Potassium Efflux and Nek7 in Pasteurella multocida-Induced NLRP3 Inflammasome Activation
title_sort critical role of potassium efflux and nek7 in pasteurella multocida-induced nlrp3 inflammasome activation
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957907/
https://www.ncbi.nlm.nih.gov/pubmed/35350616
http://dx.doi.org/10.3389/fmicb.2022.849482
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