Differential Roles of Interleukin-17A and -17F in Host Defense against Mucoepithelial Bacterial Infection and Allergic Responses
Interleukin-17A (IL-17A) is a cytokine produced by T helper 17 (Th17) cells and plays important roles in the development of inflammatory diseases. Although IL-17F is highly homologous to IL-17A and binds the same receptor, the functional roles of this molecule remain largely unknown. Here, we demons...
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creator | Ishigame, Harumichi Kakuta, Shigeru Nagai, Takeshi Kadoki, Motohiko Nambu, Aya Komiyama, Yutaka Fujikado, Noriyuki Tanahashi, Yuko Akitsu, Aoi Kotaki, Hayato Sudo, Katsuko Nakae, Susumu Sasakawa, Chihiro Iwakura, Yoichiro |
description | Interleukin-17A (IL-17A) is a cytokine produced by T helper 17 (Th17) cells and plays important roles in the development of inflammatory diseases. Although IL-17F is highly homologous to IL-17A and binds the same receptor, the functional roles of this molecule remain largely unknown. Here, we demonstrated with
Il17a
−/−
,
Il17f
−/−, and
Il17a
−/−Il17f
−/− mice that IL-17F played only marginal roles, if at all, in the development of delayed-type and contact hypersensitivities, autoimmune encephalomyelitis, collagen-induced arthritis, and arthritis in
Il1rn
−/− mice. In contrast, both IL-17F and IL-17A were involved in host defense against mucoepithelial infection by
Staphylococcus aureus and
Citrobacter rodentium. IL-17A was produced mainly in T cells, whereas IL-17F was produced in T cells, innate immune cells, and epithelial cells. Although only IL-17A efficiently induced cytokines in macrophages, both cytokines activated epithelial innate immune responses. These observations indicate that IL-17A and IL-17F have overlapping yet distinct roles in host immune and defense mechanisms. |
doi_str_mv | 10.1016/j.immuni.2008.11.009 |
format | Article |
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Il17a
−/−
,
Il17f
−/−, and
Il17a
−/−Il17f
−/− mice that IL-17F played only marginal roles, if at all, in the development of delayed-type and contact hypersensitivities, autoimmune encephalomyelitis, collagen-induced arthritis, and arthritis in
Il1rn
−/− mice. In contrast, both IL-17F and IL-17A were involved in host defense against mucoepithelial infection by
Staphylococcus aureus and
Citrobacter rodentium. IL-17A was produced mainly in T cells, whereas IL-17F was produced in T cells, innate immune cells, and epithelial cells. Although only IL-17A efficiently induced cytokines in macrophages, both cytokines activated epithelial innate immune responses. These observations indicate that IL-17A and IL-17F have overlapping yet distinct roles in host immune and defense mechanisms.</description><identifier>ISSN: 1074-7613</identifier><identifier>EISSN: 1097-4180</identifier><identifier>DOI: 10.1016/j.immuni.2008.11.009</identifier><identifier>PMID: 19144317</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Arthritis ; Arthritis - genetics ; Arthritis - immunology ; Bacterial infections ; Bacterial Infections - immunology ; Bacterial Infections - prevention & control ; CELLIMMUNO ; Cells, Cultured ; Citrobacter rodentium ; Cytokines ; Cytokines - metabolism ; Flow Cytometry ; Hypersensitivity - immunology ; Immune system ; Interleukin-17 - classification ; Interleukin-17 - genetics ; Interleukin-17 - physiology ; Mice ; Mice, Knockout ; MOLIMMUNO ; Rodents ; Science ; Staphylococcus aureus ; Technological change</subject><ispartof>Immunity (Cambridge, Mass.), 2009-01, Vol.30 (1), p.108-119</ispartof><rights>2009 Elsevier Inc.</rights><rights>Copyright Elsevier Limited Jan 16, 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c582t-dce708eb6a70354319b00a787ad854a973b7b7c3c8c925d6c649d9822cc22eaf3</citedby><cites>FETCH-LOGICAL-c582t-dce708eb6a70354319b00a787ad854a973b7b7c3c8c925d6c649d9822cc22eaf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.immuni.2008.11.009$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19144317$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishigame, Harumichi</creatorcontrib><creatorcontrib>Kakuta, Shigeru</creatorcontrib><creatorcontrib>Nagai, Takeshi</creatorcontrib><creatorcontrib>Kadoki, Motohiko</creatorcontrib><creatorcontrib>Nambu, Aya</creatorcontrib><creatorcontrib>Komiyama, Yutaka</creatorcontrib><creatorcontrib>Fujikado, Noriyuki</creatorcontrib><creatorcontrib>Tanahashi, Yuko</creatorcontrib><creatorcontrib>Akitsu, Aoi</creatorcontrib><creatorcontrib>Kotaki, Hayato</creatorcontrib><creatorcontrib>Sudo, Katsuko</creatorcontrib><creatorcontrib>Nakae, Susumu</creatorcontrib><creatorcontrib>Sasakawa, Chihiro</creatorcontrib><creatorcontrib>Iwakura, Yoichiro</creatorcontrib><title>Differential Roles of Interleukin-17A and -17F in Host Defense against Mucoepithelial Bacterial Infection and Allergic Responses</title><title>Immunity (Cambridge, Mass.)</title><addtitle>Immunity</addtitle><description>Interleukin-17A (IL-17A) is a cytokine produced by T helper 17 (Th17) cells and plays important roles in the development of inflammatory diseases. Although IL-17F is highly homologous to IL-17A and binds the same receptor, the functional roles of this molecule remain largely unknown. Here, we demonstrated with
Il17a
−/−
,
Il17f
−/−, and
Il17a
−/−Il17f
−/− mice that IL-17F played only marginal roles, if at all, in the development of delayed-type and contact hypersensitivities, autoimmune encephalomyelitis, collagen-induced arthritis, and arthritis in
Il1rn
−/− mice. In contrast, both IL-17F and IL-17A were involved in host defense against mucoepithelial infection by
Staphylococcus aureus and
Citrobacter rodentium. IL-17A was produced mainly in T cells, whereas IL-17F was produced in T cells, innate immune cells, and epithelial cells. Although only IL-17A efficiently induced cytokines in macrophages, both cytokines activated epithelial innate immune responses. These observations indicate that IL-17A and IL-17F have overlapping yet distinct roles in host immune and defense mechanisms.</description><subject>Animals</subject><subject>Arthritis</subject><subject>Arthritis - genetics</subject><subject>Arthritis - immunology</subject><subject>Bacterial infections</subject><subject>Bacterial Infections - immunology</subject><subject>Bacterial Infections - prevention & control</subject><subject>CELLIMMUNO</subject><subject>Cells, Cultured</subject><subject>Citrobacter rodentium</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Flow Cytometry</subject><subject>Hypersensitivity - immunology</subject><subject>Immune system</subject><subject>Interleukin-17 - classification</subject><subject>Interleukin-17 - genetics</subject><subject>Interleukin-17 - physiology</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>MOLIMMUNO</subject><subject>Rodents</subject><subject>Science</subject><subject>Staphylococcus aureus</subject><subject>Technological change</subject><issn>1074-7613</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd9r1TAUx4sobk7_A5GA4FvrSZvmx4tw3Zy7sDEY-hzS9HTm2ibXpBV8259u6r0g7EGfcgKf88nJ-RbFawoVBcrf7yo3TYt3VQ0gK0orAPWkOKWgRMmohKdrLVgpOG1Oihcp7QAoaxU8L06ooow1VJwWDxduGDCin50ZyV0YMZEwkK2fMY64fHe-pGJDjO9JLi6J8-QqpJlc4IA-ITH3xvl8v1lswL2bv-G4ij4amwVrtfUD2tkF_8exGUeM986SO0z7kAXpZfFsMGPCV8fzrPh6-enL-VV5fft5e765Lm0r67nsLQqQ2HEjoGnz7KoDMEIK08uWGSWaTnTCNlZaVbc9t5ypXsm6trau0QzNWfHu4N3H8GPBNOvJJYvjaDyGJWnOJVXA2v-CNTRctEpl8O0jcBeW6PMnNG2B1TxzPFPsQNkYUoo46H10k4m_NAW9Bql3-hCkXoPUlOocZG57c5Qv3YT936Zjchn4cAAwL-2nw6iTdegt9i7mhes-uH-_8Bumk7BB</recordid><startdate>20090116</startdate><enddate>20090116</enddate><creator>Ishigame, Harumichi</creator><creator>Kakuta, Shigeru</creator><creator>Nagai, Takeshi</creator><creator>Kadoki, Motohiko</creator><creator>Nambu, Aya</creator><creator>Komiyama, Yutaka</creator><creator>Fujikado, Noriyuki</creator><creator>Tanahashi, Yuko</creator><creator>Akitsu, Aoi</creator><creator>Kotaki, Hayato</creator><creator>Sudo, Katsuko</creator><creator>Nakae, Susumu</creator><creator>Sasakawa, Chihiro</creator><creator>Iwakura, Yoichiro</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><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>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20090116</creationdate><title>Differential Roles of Interleukin-17A and -17F in Host Defense against Mucoepithelial Bacterial Infection and Allergic Responses</title><author>Ishigame, Harumichi ; Kakuta, Shigeru ; Nagai, Takeshi ; Kadoki, Motohiko ; Nambu, Aya ; Komiyama, Yutaka ; Fujikado, Noriyuki ; Tanahashi, Yuko ; Akitsu, Aoi ; Kotaki, Hayato ; Sudo, Katsuko ; Nakae, Susumu ; Sasakawa, Chihiro ; Iwakura, Yoichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c582t-dce708eb6a70354319b00a787ad854a973b7b7c3c8c925d6c649d9822cc22eaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Arthritis</topic><topic>Arthritis - genetics</topic><topic>Arthritis - immunology</topic><topic>Bacterial infections</topic><topic>Bacterial Infections - immunology</topic><topic>Bacterial Infections - prevention & control</topic><topic>CELLIMMUNO</topic><topic>Cells, Cultured</topic><topic>Citrobacter rodentium</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>Flow Cytometry</topic><topic>Hypersensitivity - immunology</topic><topic>Immune system</topic><topic>Interleukin-17 - classification</topic><topic>Interleukin-17 - genetics</topic><topic>Interleukin-17 - physiology</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>MOLIMMUNO</topic><topic>Rodents</topic><topic>Science</topic><topic>Staphylococcus aureus</topic><topic>Technological change</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishigame, Harumichi</creatorcontrib><creatorcontrib>Kakuta, Shigeru</creatorcontrib><creatorcontrib>Nagai, Takeshi</creatorcontrib><creatorcontrib>Kadoki, Motohiko</creatorcontrib><creatorcontrib>Nambu, Aya</creatorcontrib><creatorcontrib>Komiyama, Yutaka</creatorcontrib><creatorcontrib>Fujikado, Noriyuki</creatorcontrib><creatorcontrib>Tanahashi, Yuko</creatorcontrib><creatorcontrib>Akitsu, Aoi</creatorcontrib><creatorcontrib>Kotaki, Hayato</creatorcontrib><creatorcontrib>Sudo, Katsuko</creatorcontrib><creatorcontrib>Nakae, Susumu</creatorcontrib><creatorcontrib>Sasakawa, Chihiro</creatorcontrib><creatorcontrib>Iwakura, Yoichiro</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids 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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Immunity (Cambridge, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishigame, Harumichi</au><au>Kakuta, Shigeru</au><au>Nagai, Takeshi</au><au>Kadoki, Motohiko</au><au>Nambu, Aya</au><au>Komiyama, Yutaka</au><au>Fujikado, Noriyuki</au><au>Tanahashi, Yuko</au><au>Akitsu, Aoi</au><au>Kotaki, Hayato</au><au>Sudo, Katsuko</au><au>Nakae, Susumu</au><au>Sasakawa, Chihiro</au><au>Iwakura, Yoichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Roles of Interleukin-17A and -17F in Host Defense against Mucoepithelial Bacterial Infection and Allergic Responses</atitle><jtitle>Immunity (Cambridge, Mass.)</jtitle><addtitle>Immunity</addtitle><date>2009-01-16</date><risdate>2009</risdate><volume>30</volume><issue>1</issue><spage>108</spage><epage>119</epage><pages>108-119</pages><issn>1074-7613</issn><eissn>1097-4180</eissn><abstract>Interleukin-17A (IL-17A) is a cytokine produced by T helper 17 (Th17) cells and plays important roles in the development of inflammatory diseases. Although IL-17F is highly homologous to IL-17A and binds the same receptor, the functional roles of this molecule remain largely unknown. Here, we demonstrated with
Il17a
−/−
,
Il17f
−/−, and
Il17a
−/−Il17f
−/− mice that IL-17F played only marginal roles, if at all, in the development of delayed-type and contact hypersensitivities, autoimmune encephalomyelitis, collagen-induced arthritis, and arthritis in
Il1rn
−/− mice. In contrast, both IL-17F and IL-17A were involved in host defense against mucoepithelial infection by
Staphylococcus aureus and
Citrobacter rodentium. IL-17A was produced mainly in T cells, whereas IL-17F was produced in T cells, innate immune cells, and epithelial cells. Although only IL-17A efficiently induced cytokines in macrophages, both cytokines activated epithelial innate immune responses. These observations indicate that IL-17A and IL-17F have overlapping yet distinct roles in host immune and defense mechanisms.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19144317</pmid><doi>10.1016/j.immuni.2008.11.009</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Cell Press Free Archives; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Arthritis Arthritis - genetics Arthritis - immunology Bacterial infections Bacterial Infections - immunology Bacterial Infections - prevention & control CELLIMMUNO Cells, Cultured Citrobacter rodentium Cytokines Cytokines - metabolism Flow Cytometry Hypersensitivity - immunology Immune system Interleukin-17 - classification Interleukin-17 - genetics Interleukin-17 - physiology Mice Mice, Knockout MOLIMMUNO Rodents Science Staphylococcus aureus Technological change |
title | Differential Roles of Interleukin-17A and -17F in Host Defense against Mucoepithelial Bacterial Infection and Allergic Responses |
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