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 |
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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 ; 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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b425t-6c07beb1eac8cd50c5cbd5bb8f20013e43ce7642d35bbe0ed28adde6cd198dd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adaptive Immunity</topic><topic>Animals</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>Cell Communication - immunology</topic><topic>Cell Differentiation - immunology</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Cigarettes</topic><topic>Coculture Techniques</topic><topic>Cytokines</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - immunology</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Emphysema</topic><topic>Extracellular Traps - immunology</topic><topic>Flow cytometry</topic><topic>Immunity, Innate</topic><topic>Inflammation</topic><topic>Inflammation - immunology</topic><topic>Laboratory animals</topic><topic>Lung diseases</topic><topic>Lupus</topic><topic>Lymphocytes</topic><topic>Male</topic><topic>Mice, Inbred BALB C</topic><topic>Neutrophils</topic><topic>Neutrophils - immunology</topic><topic>Pathogenesis</topic><topic>Pulmonary Emphysema - etiology</topic><topic>Pulmonary Emphysema - immunology</topic><topic>Smoking</topic><topic>Studies</topic><topic>Th1 Cells - immunology</topic><topic>Th17 Cells - immunology</topic><topic>Tobacco smoke</topic><topic>Tobacco Smoke Pollution - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Thorax</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qiu, Shi-Lin</au><au>Zhang, Hui</au><au>Tang, Qi-ya</au><au>Bai, Jing</au><au>He, Zhi-Yi</au><au>Zhang, Jian-Quan</au><au>Li, Mei-Hua</au><au>Deng, Jing-Min</au><au>Liu, Guang-Nan</au><au>Zhong, Xiao-Ning</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neutrophil extracellular traps induced by cigarette smoke activate plasmacytoid dendritic cells</atitle><jtitle>Thorax</jtitle><addtitle>Thorax</addtitle><date>2017-12</date><risdate>2017</risdate><volume>72</volume><issue>12</issue><spage>1084</spage><epage>1093</epage><pages>1084-1093</pages><issn>0040-6376</issn><eissn>1468-3296</eissn><abstract>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.</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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