Lung natural killer cells in mice: phenotype and response to respiratory infection

Summary Natural killer (NK) cells have a specialized function in peripheral organs, which is determined by the organ‐specific niches. We have attempted to explore whether lung NK cells display a particular phenotype according to their function in the unique pulmonary environment in health or during...

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Veröffentlicht in:Immunology 2012-09, Vol.137 (1), p.37-47
Hauptverfasser: Wang, Jian, Li, Fengqi, Zheng, Meijuan, Sun, Rui, Wei, Haiming, Tian, Zhigang
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container_issue 1
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container_title Immunology
container_volume 137
creator Wang, Jian
Li, Fengqi
Zheng, Meijuan
Sun, Rui
Wei, Haiming
Tian, Zhigang
description Summary Natural killer (NK) cells have a specialized function in peripheral organs, which is determined by the organ‐specific niches. We have attempted to explore whether lung NK cells display a particular phenotype according to their function in the unique pulmonary environment in health or during respiratory infection in mice. In healthy mice, higher frequencies of NK cells among lymphocytes were detected in the lung than in other tissues (lymph node, bone marrow, spleen, blood and liver), and lung NK cells maintained a more mature phenotype, implying that lung NK cells were critical for the pulmonary immune response. However, lung NK cells expressed higher levels of inhibitory receptors and lower levels of activating receptors, migration/adhesion‐associated molecules and co‐stimulatory molecules than splenic NK cells, implying that lung NK cells were quiescent, and the activation of lung NK cells was tightly regulated by the pulmonary environment in health. During respiratory infection, lung NK cells could be activated and express functional molecules (CD107a and interferon‐γ) to take part in the response to infection quickly. These results suggested that the unique pulmonary environment promotes the development of NK cells with a lung‐specific phenotype.
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We have attempted to explore whether lung NK cells display a particular phenotype according to their function in the unique pulmonary environment in health or during respiratory infection in mice. In healthy mice, higher frequencies of NK cells among lymphocytes were detected in the lung than in other tissues (lymph node, bone marrow, spleen, blood and liver), and lung NK cells maintained a more mature phenotype, implying that lung NK cells were critical for the pulmonary immune response. However, lung NK cells expressed higher levels of inhibitory receptors and lower levels of activating receptors, migration/adhesion‐associated molecules and co‐stimulatory molecules than splenic NK cells, implying that lung NK cells were quiescent, and the activation of lung NK cells was tightly regulated by the pulmonary environment in health. During respiratory infection, lung NK cells could be activated and express functional molecules (CD107a and interferon‐γ) to take part in the response to infection quickly. These results suggested that the unique pulmonary environment promotes the development of NK cells with a lung‐specific phenotype.</description><identifier>ISSN: 0019-2805</identifier><identifier>EISSN: 1365-2567</identifier><identifier>DOI: 10.1111/j.1365-2567.2012.03607.x</identifier><identifier>PMID: 22612500</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Animals ; function ; Genotype &amp; phenotype ; Infections ; Influenza A Virus, H1N1 Subtype - immunology ; Interferon-gamma ; Killer Cells, Natural - immunology ; Klebsiella Infections - immunology ; Klebsiella pneumoniae - immunology ; Klebsiella pneumoniae - pathogenicity ; lung ; Lung - immunology ; Lymphocyte Activation - immunology ; Lymphocyte Count ; Lymphocyte receptors ; Lysosomal-Associated Membrane Protein 1 ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Miscarriage ; natural killer cells ; Original ; Orthomyxoviridae Infections - immunology ; Orthomyxoviridae Infections - virology ; Phenotype ; Respiratory Tract Infections - immunology ; Staphylococcal Infections - immunology ; Staphylococcus aureus - immunology ; Staphylococcus aureus - pathogenicity</subject><ispartof>Immunology, 2012-09, Vol.137 (1), p.37-47</ispartof><rights>2012 The Authors. 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Li, Fengqi ; Zheng, Meijuan ; Sun, Rui ; Wei, Haiming ; Tian, Zhigang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6017-d91e57bf81119877bd79c8b50b72d87ba2929c7803bb5933f9bc32139373d87d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>function</topic><topic>Genotype &amp; phenotype</topic><topic>Infections</topic><topic>Influenza A Virus, H1N1 Subtype - immunology</topic><topic>Interferon-gamma</topic><topic>Killer Cells, Natural - immunology</topic><topic>Klebsiella Infections - immunology</topic><topic>Klebsiella pneumoniae - immunology</topic><topic>Klebsiella pneumoniae - pathogenicity</topic><topic>lung</topic><topic>Lung - immunology</topic><topic>Lymphocyte Activation - immunology</topic><topic>Lymphocyte Count</topic><topic>Lymphocyte receptors</topic><topic>Lysosomal-Associated Membrane Protein 1</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Miscarriage</topic><topic>natural killer cells</topic><topic>Original</topic><topic>Orthomyxoviridae Infections - immunology</topic><topic>Orthomyxoviridae Infections - virology</topic><topic>Phenotype</topic><topic>Respiratory Tract Infections - immunology</topic><topic>Staphylococcal Infections - immunology</topic><topic>Staphylococcus aureus - immunology</topic><topic>Staphylococcus aureus - pathogenicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Jian</creatorcontrib><creatorcontrib>Li, Fengqi</creatorcontrib><creatorcontrib>Zheng, Meijuan</creatorcontrib><creatorcontrib>Sun, Rui</creatorcontrib><creatorcontrib>Wei, Haiming</creatorcontrib><creatorcontrib>Tian, Zhigang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Jian</au><au>Li, Fengqi</au><au>Zheng, Meijuan</au><au>Sun, Rui</au><au>Wei, Haiming</au><au>Tian, Zhigang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lung natural killer cells in mice: phenotype and response to respiratory infection</atitle><jtitle>Immunology</jtitle><addtitle>Immunology</addtitle><date>2012-09</date><risdate>2012</risdate><volume>137</volume><issue>1</issue><spage>37</spage><epage>47</epage><pages>37-47</pages><issn>0019-2805</issn><eissn>1365-2567</eissn><abstract>Summary Natural killer (NK) cells have a specialized function in peripheral organs, which is determined by the organ‐specific niches. We have attempted to explore whether lung NK cells display a particular phenotype according to their function in the unique pulmonary environment in health or during respiratory infection in mice. In healthy mice, higher frequencies of NK cells among lymphocytes were detected in the lung than in other tissues (lymph node, bone marrow, spleen, blood and liver), and lung NK cells maintained a more mature phenotype, implying that lung NK cells were critical for the pulmonary immune response. However, lung NK cells expressed higher levels of inhibitory receptors and lower levels of activating receptors, migration/adhesion‐associated molecules and co‐stimulatory molecules than splenic NK cells, implying that lung NK cells were quiescent, and the activation of lung NK cells was tightly regulated by the pulmonary environment in health. 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source MEDLINE; Wiley Online Library Free Content; IngentaConnect Free/Open Access Journals; EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals; PubMed Central
subjects Animals
function
Genotype & phenotype
Infections
Influenza A Virus, H1N1 Subtype - immunology
Interferon-gamma
Killer Cells, Natural - immunology
Klebsiella Infections - immunology
Klebsiella pneumoniae - immunology
Klebsiella pneumoniae - pathogenicity
lung
Lung - immunology
Lymphocyte Activation - immunology
Lymphocyte Count
Lymphocyte receptors
Lysosomal-Associated Membrane Protein 1
Male
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Miscarriage
natural killer cells
Original
Orthomyxoviridae Infections - immunology
Orthomyxoviridae Infections - virology
Phenotype
Respiratory Tract Infections - immunology
Staphylococcal Infections - immunology
Staphylococcus aureus - immunology
Staphylococcus aureus - pathogenicity
title Lung natural killer cells in mice: phenotype and response to respiratory infection
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