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Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4

The potD gene, belonging to the well-conserved ABC (ATP-binding cassette) transport system potABCD, encodes the bacterial substrate-binding subunit of the polyamine transport system. In this study, we found PotD in Haemophilus (Glaesserella) parasuis could actively stimulate both humoral immune and...

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Autores principales: Dai, Ke, Ma, Xiaoyu, Yang, Zhen, Chang, Yung-Fu, Cao, Sanjie, Zhao, Qin, Huang, Xiaobo, Wu, Rui, Huang, Yong, Yan, Qigui, Han, Xinfeng, Ma, Xiaoping, Wen, Xintian, Wen, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963478/
https://www.ncbi.nlm.nih.gov/pubmed/31847381
http://dx.doi.org/10.3390/vaccines7040216
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author Dai, Ke
Ma, Xiaoyu
Yang, Zhen
Chang, Yung-Fu
Cao, Sanjie
Zhao, Qin
Huang, Xiaobo
Wu, Rui
Huang, Yong
Yan, Qigui
Han, Xinfeng
Ma, Xiaoping
Wen, Xintian
Wen, Yiping
author_facet Dai, Ke
Ma, Xiaoyu
Yang, Zhen
Chang, Yung-Fu
Cao, Sanjie
Zhao, Qin
Huang, Xiaobo
Wu, Rui
Huang, Yong
Yan, Qigui
Han, Xinfeng
Ma, Xiaoping
Wen, Xintian
Wen, Yiping
author_sort Dai, Ke
collection PubMed
description The potD gene, belonging to the well-conserved ABC (ATP-binding cassette) transport system potABCD, encodes the bacterial substrate-binding subunit of the polyamine transport system. In this study, we found PotD in Haemophilus (Glaesserella) parasuis could actively stimulate both humoral immune and cellular immune responses and elevate lymphocyte proliferation, thus eliciting a Th1-type immune response in a murine immunity and infection model. Stimulation of Raw 264.7 macrophages with PotD validated that Toll-like receptor 4, rather than 2, participated in the positive transcription and expression of pro-inflammatory cytokines IL–1β, IL–6, and TNF–α using qPCR and ELISA. Blocking signal-regulated JNK–MAPK and RelA(p65) pathways significantly decreased PotD-induced pro-inflammatory cytokine production. Overall, we conclude that vaccination of PotD could induce both humoral and cellular immune responses and provide immunoprotection against H. parasuis challenge. The data also suggest that Glaesserella PotD is a novel pro-inflammatory mediator and induces TLR4-dependent pro-inflammatory activity in Raw 264.7 macrophages through JNK–MAPK and RelA(p65) pathways.
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spelling pubmed-69634782020-01-30 Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4 Dai, Ke Ma, Xiaoyu Yang, Zhen Chang, Yung-Fu Cao, Sanjie Zhao, Qin Huang, Xiaobo Wu, Rui Huang, Yong Yan, Qigui Han, Xinfeng Ma, Xiaoping Wen, Xintian Wen, Yiping Vaccines (Basel) Article The potD gene, belonging to the well-conserved ABC (ATP-binding cassette) transport system potABCD, encodes the bacterial substrate-binding subunit of the polyamine transport system. In this study, we found PotD in Haemophilus (Glaesserella) parasuis could actively stimulate both humoral immune and cellular immune responses and elevate lymphocyte proliferation, thus eliciting a Th1-type immune response in a murine immunity and infection model. Stimulation of Raw 264.7 macrophages with PotD validated that Toll-like receptor 4, rather than 2, participated in the positive transcription and expression of pro-inflammatory cytokines IL–1β, IL–6, and TNF–α using qPCR and ELISA. Blocking signal-regulated JNK–MAPK and RelA(p65) pathways significantly decreased PotD-induced pro-inflammatory cytokine production. Overall, we conclude that vaccination of PotD could induce both humoral and cellular immune responses and provide immunoprotection against H. parasuis challenge. The data also suggest that Glaesserella PotD is a novel pro-inflammatory mediator and induces TLR4-dependent pro-inflammatory activity in Raw 264.7 macrophages through JNK–MAPK and RelA(p65) pathways. MDPI 2019-12-14 /pmc/articles/PMC6963478/ /pubmed/31847381 http://dx.doi.org/10.3390/vaccines7040216 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dai, Ke
Ma, Xiaoyu
Yang, Zhen
Chang, Yung-Fu
Cao, Sanjie
Zhao, Qin
Huang, Xiaobo
Wu, Rui
Huang, Yong
Yan, Qigui
Han, Xinfeng
Ma, Xiaoping
Wen, Xintian
Wen, Yiping
Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4
title Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4
title_full Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4
title_fullStr Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4
title_full_unstemmed Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4
title_short Polyamine Transport Protein PotD Protects Mice against Haemophilus parasuis and Elevates the Secretion of Pro-Inflammatory Cytokines of Macrophage via JNK–MAPK and NF–κB Signal Pathways through TLR4
title_sort polyamine transport protein potd protects mice against haemophilus parasuis and elevates the secretion of pro-inflammatory cytokines of macrophage via jnk–mapk and nf–κb signal pathways through tlr4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963478/
https://www.ncbi.nlm.nih.gov/pubmed/31847381
http://dx.doi.org/10.3390/vaccines7040216
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