Neutrophil extracellular traps induced by cigarette smoke activate plasmacytoid dendritic cells

BackgroundNeutrophil extracellular traps (NETs) represent a distinct strategy by which neutrophils trap, confine and eliminate invading microorganisms. Emerging evidence suggests that NETs exert a deleterious effect to the host in the absence of microbial stimuli. However, the role of NETs in smokin...

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Veröffentlicht in:Thorax 2017-12, Vol.72 (12), p.1084-1093
Hauptverfasser: Qiu, Shi-Lin, Zhang, Hui, Tang, Qi-ya, Bai, Jing, He, Zhi-Yi, Zhang, Jian-Quan, Li, Mei-Hua, Deng, Jing-Min, Liu, Guang-Nan, Zhong, Xiao-Ning
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container_end_page 1093
container_issue 12
container_start_page 1084
container_title Thorax
container_volume 72
creator Qiu, Shi-Lin
Zhang, Hui
Tang, Qi-ya
Bai, Jing
He, Zhi-Yi
Zhang, Jian-Quan
Li, Mei-Hua
Deng, Jing-Min
Liu, Guang-Nan
Zhong, Xiao-Ning
description BackgroundNeutrophil extracellular traps (NETs) represent a distinct strategy by which neutrophils trap, confine and eliminate invading microorganisms. Emerging evidence suggests that NETs exert a deleterious effect to the host in the absence of microbial stimuli. However, the role of NETs in smoking-related lung diseases remains to be elucidated.ObjectivesTo evaluate the formation of NETs in the context of chronic inflammation induced by cigarette smoking and explore its potential role in an experimental mouse model of emphysema.MethodsThe formation and degradation of NETs in cigarette smoke exposed mice was assessed with a fluorescence microscope. The potential influences of NETs on plasmacytoiddendritic cells were also investigated.ResultsNETs were more prone to formation by polymorphonuclearneutrophils but defective in degradation in cigarette smoke exposed mice. Cigarette smoke extract (CSE) served as an important facilitator that triggered neutrophils to undergo NETosis in vitro. Furthermore, CSE-induced NETs were capable of driving plasmacytoiddendritic cell maturation and activation, thereby initiating a T-cell-mediated immune response.ConclusionsNETs may represent a critical connection between innate and adaptive immune responses under conditions of chronic inflammation induced by cigarette smoke exposure.
doi_str_mv 10.1136/thoraxjnl-2016-209887
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Emerging evidence suggests that NETs exert a deleterious effect to the host in the absence of microbial stimuli. However, the role of NETs in smoking-related lung diseases remains to be elucidated.ObjectivesTo evaluate the formation of NETs in the context of chronic inflammation induced by cigarette smoking and explore its potential role in an experimental mouse model of emphysema.MethodsThe formation and degradation of NETs in cigarette smoke exposed mice was assessed with a fluorescence microscope. The potential influences of NETs on plasmacytoiddendritic cells were also investigated.ResultsNETs were more prone to formation by polymorphonuclearneutrophils but defective in degradation in cigarette smoke exposed mice. Cigarette smoke extract (CSE) served as an important facilitator that triggered neutrophils to undergo NETosis in vitro. Furthermore, CSE-induced NETs were capable of driving plasmacytoiddendritic cell maturation and activation, thereby initiating a T-cell-mediated immune response.ConclusionsNETs may represent a critical connection between innate and adaptive immune responses under conditions of chronic inflammation induced by cigarette smoke exposure.</description><identifier>ISSN: 0040-6376</identifier><identifier>EISSN: 1468-3296</identifier><identifier>DOI: 10.1136/thoraxjnl-2016-209887</identifier><identifier>PMID: 28720648</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Adaptive Immunity ; Animals ; CD4-Positive T-Lymphocytes - immunology ; Cell Communication - immunology ; Cell Differentiation - immunology ; Chronic obstructive pulmonary disease ; Cigarettes ; Coculture Techniques ; Cytokines ; Dendritic cells ; Dendritic Cells - immunology ; Deoxyribonucleic acid ; DNA ; Emphysema ; Extracellular Traps - immunology ; Flow cytometry ; Immunity, Innate ; Inflammation ; Inflammation - immunology ; Laboratory animals ; Lung diseases ; Lupus ; Lymphocytes ; Male ; Mice, Inbred BALB C ; Neutrophils ; Neutrophils - immunology ; Pathogenesis ; Pulmonary Emphysema - etiology ; Pulmonary Emphysema - immunology ; Smoking ; Studies ; Th1 Cells - immunology ; Th17 Cells - immunology ; Tobacco smoke ; Tobacco Smoke Pollution - adverse effects</subject><ispartof>Thorax, 2017-12, Vol.72 (12), p.1084-1093</ispartof><rights>Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.</rights><rights>Copyright: 2017 © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b425t-6c07beb1eac8cd50c5cbd5bb8f20013e43ce7642d35bbe0ed28adde6cd198dd13</citedby><cites>FETCH-LOGICAL-b425t-6c07beb1eac8cd50c5cbd5bb8f20013e43ce7642d35bbe0ed28adde6cd198dd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28720648$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qiu, Shi-Lin</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Tang, Qi-ya</creatorcontrib><creatorcontrib>Bai, Jing</creatorcontrib><creatorcontrib>He, Zhi-Yi</creatorcontrib><creatorcontrib>Zhang, Jian-Quan</creatorcontrib><creatorcontrib>Li, Mei-Hua</creatorcontrib><creatorcontrib>Deng, Jing-Min</creatorcontrib><creatorcontrib>Liu, Guang-Nan</creatorcontrib><creatorcontrib>Zhong, Xiao-Ning</creatorcontrib><title>Neutrophil extracellular traps induced by cigarette smoke activate plasmacytoid dendritic cells</title><title>Thorax</title><addtitle>Thorax</addtitle><description>BackgroundNeutrophil extracellular traps (NETs) represent a distinct strategy by which neutrophils trap, confine and eliminate invading microorganisms. Emerging evidence suggests that NETs exert a deleterious effect to the host in the absence of microbial stimuli. However, the role of NETs in smoking-related lung diseases remains to be elucidated.ObjectivesTo evaluate the formation of NETs in the context of chronic inflammation induced by cigarette smoking and explore its potential role in an experimental mouse model of emphysema.MethodsThe formation and degradation of NETs in cigarette smoke exposed mice was assessed with a fluorescence microscope. The potential influences of NETs on plasmacytoiddendritic cells were also investigated.ResultsNETs were more prone to formation by polymorphonuclearneutrophils but defective in degradation in cigarette smoke exposed mice. Cigarette smoke extract (CSE) served as an important facilitator that triggered neutrophils to undergo NETosis in vitro. Furthermore, CSE-induced NETs were capable of driving plasmacytoiddendritic cell maturation and activation, thereby initiating a T-cell-mediated immune response.ConclusionsNETs may represent a critical connection between innate and adaptive immune responses under conditions of chronic inflammation induced by cigarette smoke exposure.</description><subject>Adaptive Immunity</subject><subject>Animals</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>Cell Communication - immunology</subject><subject>Cell Differentiation - immunology</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Cigarettes</subject><subject>Coculture Techniques</subject><subject>Cytokines</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - immunology</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Emphysema</subject><subject>Extracellular Traps - immunology</subject><subject>Flow cytometry</subject><subject>Immunity, Innate</subject><subject>Inflammation</subject><subject>Inflammation - immunology</subject><subject>Laboratory animals</subject><subject>Lung diseases</subject><subject>Lupus</subject><subject>Lymphocytes</subject><subject>Male</subject><subject>Mice, Inbred BALB C</subject><subject>Neutrophils</subject><subject>Neutrophils - immunology</subject><subject>Pathogenesis</subject><subject>Pulmonary Emphysema - etiology</subject><subject>Pulmonary Emphysema - immunology</subject><subject>Smoking</subject><subject>Studies</subject><subject>Th1 Cells - immunology</subject><subject>Th17 Cells - immunology</subject><subject>Tobacco smoke</subject><subject>Tobacco Smoke Pollution - adverse effects</subject><issn>0040-6376</issn><issn>1468-3296</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkMtOwzAQRS0EoqXwCSBLrANjJ3GcJap4SQg2sLb8mNKUpAm2g9q_J1FL12zmpXvvSIeQSwY3jKXiNi5brzerdZ1wYGIopZTFEZmyTMgk5aU4JlOADBKRFmJCzkJYAYBkrDglEy4LDiKTU6JesY--7ZZVTXETvbZY132tPR3mLtBq7XqLjpottdWn9hgj0tC0X0i1jdWPHtau1qHRdhvbylGHa-erWFk6JoVzcrLQdcCLfZ-Rj4f79_lT8vL2-Dy_e0lMxvOYCAuFQcNQW2ldDja3xuXGyAUHYClmqcVCZNylwxEBHZfaORTWsVI6x9IZud7ldr797jFEtWp7vx5eKlYWUPLRPajyncr6NgSPC9X5qtF-qxioEas6YFUjVrXDOviu9um9adAdXH8cBwHsBKZZ_TPzFwRziVM</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Qiu, Shi-Lin</creator><creator>Zhang, Hui</creator><creator>Tang, Qi-ya</creator><creator>Bai, Jing</creator><creator>He, Zhi-Yi</creator><creator>Zhang, Jian-Quan</creator><creator>Li, Mei-Hua</creator><creator>Deng, Jing-Min</creator><creator>Liu, Guang-Nan</creator><creator>Zhong, Xiao-Ning</creator><general>BMJ Publishing Group LTD</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201712</creationdate><title>Neutrophil extracellular traps induced by cigarette smoke activate plasmacytoid dendritic cells</title><author>Qiu, Shi-Lin ; 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Emerging evidence suggests that NETs exert a deleterious effect to the host in the absence of microbial stimuli. However, the role of NETs in smoking-related lung diseases remains to be elucidated.ObjectivesTo evaluate the formation of NETs in the context of chronic inflammation induced by cigarette smoking and explore its potential role in an experimental mouse model of emphysema.MethodsThe formation and degradation of NETs in cigarette smoke exposed mice was assessed with a fluorescence microscope. The potential influences of NETs on plasmacytoiddendritic cells were also investigated.ResultsNETs were more prone to formation by polymorphonuclearneutrophils but defective in degradation in cigarette smoke exposed mice. Cigarette smoke extract (CSE) served as an important facilitator that triggered neutrophils to undergo NETosis in vitro. Furthermore, CSE-induced NETs were capable of driving plasmacytoiddendritic cell maturation and activation, thereby initiating a T-cell-mediated immune response.ConclusionsNETs may represent a critical connection between innate and adaptive immune responses under conditions of chronic inflammation induced by cigarette smoke exposure.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>28720648</pmid><doi>10.1136/thoraxjnl-2016-209887</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Adaptive Immunity
Animals
CD4-Positive T-Lymphocytes - immunology
Cell Communication - immunology
Cell Differentiation - immunology
Chronic obstructive pulmonary disease
Cigarettes
Coculture Techniques
Cytokines
Dendritic cells
Dendritic Cells - immunology
Deoxyribonucleic acid
DNA
Emphysema
Extracellular Traps - immunology
Flow cytometry
Immunity, Innate
Inflammation
Inflammation - immunology
Laboratory animals
Lung diseases
Lupus
Lymphocytes
Male
Mice, Inbred BALB C
Neutrophils
Neutrophils - immunology
Pathogenesis
Pulmonary Emphysema - etiology
Pulmonary Emphysema - immunology
Smoking
Studies
Th1 Cells - immunology
Th17 Cells - immunology
Tobacco smoke
Tobacco Smoke Pollution - adverse effects
title Neutrophil extracellular traps induced by cigarette smoke activate plasmacytoid dendritic cells
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