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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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. |
doi_str_mv | 10.1111/j.1365-2567.2012.03607.x |
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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.</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 & 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. Immunology © 2012 Blackwell Publishing Ltd</rights><rights>2012 The Authors. Immunology © 2012 Blackwell Publishing Ltd.</rights><rights>Copyright © 2012 Blackwell Publishing Ltd</rights><rights>Copyright © 2012 Blackwell Publishing Ltd 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6017-d91e57bf81119877bd79c8b50b72d87ba2929c7803bb5933f9bc32139373d87d3</citedby><cites>FETCH-LOGICAL-c6017-d91e57bf81119877bd79c8b50b72d87ba2929c7803bb5933f9bc32139373d87d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449245/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449245/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1416,1432,27922,27923,45572,45573,46407,46831,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22612500$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Jian</creatorcontrib><creatorcontrib>Li, Fengqi</creatorcontrib><creatorcontrib>Zheng, Meijuan</creatorcontrib><creatorcontrib>Sun, Rui</creatorcontrib><creatorcontrib>Wei, Haiming</creatorcontrib><creatorcontrib>Tian, Zhigang</creatorcontrib><title>Lung natural killer cells in mice: phenotype and response to respiratory infection</title><title>Immunology</title><addtitle>Immunology</addtitle><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.</description><subject>Animals</subject><subject>function</subject><subject>Genotype & phenotype</subject><subject>Infections</subject><subject>Influenza A Virus, H1N1 Subtype - immunology</subject><subject>Interferon-gamma</subject><subject>Killer Cells, Natural - immunology</subject><subject>Klebsiella Infections - immunology</subject><subject>Klebsiella pneumoniae - immunology</subject><subject>Klebsiella pneumoniae - pathogenicity</subject><subject>lung</subject><subject>Lung - immunology</subject><subject>Lymphocyte Activation - immunology</subject><subject>Lymphocyte Count</subject><subject>Lymphocyte receptors</subject><subject>Lysosomal-Associated Membrane Protein 1</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Miscarriage</subject><subject>natural killer cells</subject><subject>Original</subject><subject>Orthomyxoviridae Infections - immunology</subject><subject>Orthomyxoviridae Infections - virology</subject><subject>Phenotype</subject><subject>Respiratory Tract Infections - immunology</subject><subject>Staphylococcal Infections - immunology</subject><subject>Staphylococcus aureus - immunology</subject><subject>Staphylococcus aureus - pathogenicity</subject><issn>0019-2805</issn><issn>1365-2567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV9rFDEUxYNY7Fr9ChLwxZcZ82cySQQFKVYLWwpFn0OSybRZZ5MxmdHut2-mWxftU_OSG-7vHnLuAQBiVONy3m9qTFtWEdbymiBMakRbxOvbZ2B1aDwHK4SwrIhA7Bi8zHlTnhQx9gIcE9JiwhBagav1HK5h0NOc9AB_-mFwCVo3DBn6ALfeug9wvHEhTrvRQR06mFweY8gOTvG-9klPMe0K3js7-RhegaNeD9m9frhPwI-zL99Pv1Xry6_np5_XlW0R5lUnsWPc9KIYkoJz03FphWHIcNIJbjSRRFouEDWGSUp7aSwlmErKael39AR82uuOs9m6zrowFQ9qTH6r005F7dX_neBv1HX8rWjTSNKwIvDuQSDFX7PLk9r6vHjXwcU5K4yoaJFgmDwFLSstoCzo20foJs4plE0ozFuBSjZNUyixp2yKOSfXH_6NkVoyVhu1RKmWKNWSsbrPWN2W0Tf_-j4M_g21AB_3wB8_uN2ThdX5xcVS0TtkibSg</recordid><startdate>201209</startdate><enddate>201209</enddate><creator>Wang, Jian</creator><creator>Li, Fengqi</creator><creator>Zheng, Meijuan</creator><creator>Sun, Rui</creator><creator>Wei, Haiming</creator><creator>Tian, Zhigang</creator><general>Wiley Subscription Services, Inc</general><general>Blackwell Science Inc</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>7QL</scope><scope>7QR</scope><scope>7T5</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201209</creationdate><title>Lung natural killer cells in mice: phenotype and response to respiratory infection</title><author>Wang, Jian ; 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 & 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. 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.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>22612500</pmid><doi>10.1111/j.1365-2567.2012.03607.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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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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