Cathelicidin Antimicrobial Peptides Block Dendritic Cell TLR4 Activation and Allergic Contact Sensitization
Cathelicidins are antimicrobial peptides of the innate immune system that establish an antimicrobial barrier at epithelial interfaces and have been proposed to have a proinflammatory function. We studied the role of cathelicidin in allergic contact dermatitis, a model requiring dendritic cells of th...
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Veröffentlicht in: | Journal of Immunology 2007-02, Vol.178 (3), p.1829-1834 |
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creator | Di Nardo, Anna Braff, Marissa H Taylor, Kristen R Na, ChangRim Granstein, Richard D McInturff, Jamie E Krutzik, Stephan Modlin, Robert L Gallo, Richard L |
description | Cathelicidins are antimicrobial peptides of the innate immune system that establish an antimicrobial barrier at epithelial interfaces and have been proposed to have a proinflammatory function. We studied the role of cathelicidin in allergic contact dermatitis, a model requiring dendritic cells of the innate immune response and T cells of the adaptive immune response. Deletion of the murine cathelicidin gene Cnlp enhanced an allergic contact response, whereas local administration of cathelicidin before sensitization inhibited the allergic response. Cathelicidins inhibited TLR4 but not TLR2 mediated induction of dendritic cell maturation and cytokine release, and this inhibition was associated with an alteration of cell membrane function and structure. Further analysis in vivo connected these observations because inhibition of sensitization by exogenous cathelicidin was dependent on the presence of functional TLR4. These observations provide evidence that cathelicidin antimicrobial peptides mediate an anti-inflammatory response in part by their activity at the membrane. |
doi_str_mv | 10.4049/jimmunol.178.3.1829 |
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We studied the role of cathelicidin in allergic contact dermatitis, a model requiring dendritic cells of the innate immune response and T cells of the adaptive immune response. Deletion of the murine cathelicidin gene Cnlp enhanced an allergic contact response, whereas local administration of cathelicidin before sensitization inhibited the allergic response. Cathelicidins inhibited TLR4 but not TLR2 mediated induction of dendritic cell maturation and cytokine release, and this inhibition was associated with an alteration of cell membrane function and structure. Further analysis in vivo connected these observations because inhibition of sensitization by exogenous cathelicidin was dependent on the presence of functional TLR4. These observations provide evidence that cathelicidin antimicrobial peptides mediate an anti-inflammatory response in part by their activity at the membrane.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>EISSN: 1365-2567</identifier><identifier>DOI: 10.4049/jimmunol.178.3.1829</identifier><identifier>PMID: 17237433</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Anti-Inflammatory Agents ; Antimicrobial Cationic Peptides - pharmacology ; Cytokines ; Dendritic Cells - drug effects ; Dendritic Cells - immunology ; Dermatitis, Allergic Contact - drug therapy ; Dermatitis, Allergic Contact - etiology ; Dermatitis, Allergic Contact - prevention & control ; Humans ; Immunity ; Mice ; Mice, Knockout ; T-Lymphocytes - immunology ; Toll-Like Receptor 4 - immunology ; Toll-Like Receptor 4 - metabolism</subject><ispartof>Journal of Immunology, 2007-02, Vol.178 (3), p.1829-1834</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-ba8a60f9026b643d160a5bdc44ae57db90627f656fc421ff3e9f3c98ed319cd93</citedby><cites>FETCH-LOGICAL-c432t-ba8a60f9026b643d160a5bdc44ae57db90627f656fc421ff3e9f3c98ed319cd93</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/17237433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Di Nardo, Anna</creatorcontrib><creatorcontrib>Braff, Marissa H</creatorcontrib><creatorcontrib>Taylor, Kristen R</creatorcontrib><creatorcontrib>Na, ChangRim</creatorcontrib><creatorcontrib>Granstein, Richard D</creatorcontrib><creatorcontrib>McInturff, Jamie E</creatorcontrib><creatorcontrib>Krutzik, Stephan</creatorcontrib><creatorcontrib>Modlin, Robert L</creatorcontrib><creatorcontrib>Gallo, Richard L</creatorcontrib><title>Cathelicidin Antimicrobial Peptides Block Dendritic Cell TLR4 Activation and Allergic Contact Sensitization</title><title>Journal of Immunology</title><addtitle>J Immunol</addtitle><description>Cathelicidins are antimicrobial peptides of the innate immune system that establish an antimicrobial barrier at epithelial interfaces and have been proposed to have a proinflammatory function. We studied the role of cathelicidin in allergic contact dermatitis, a model requiring dendritic cells of the innate immune response and T cells of the adaptive immune response. Deletion of the murine cathelicidin gene Cnlp enhanced an allergic contact response, whereas local administration of cathelicidin before sensitization inhibited the allergic response. Cathelicidins inhibited TLR4 but not TLR2 mediated induction of dendritic cell maturation and cytokine release, and this inhibition was associated with an alteration of cell membrane function and structure. Further analysis in vivo connected these observations because inhibition of sensitization by exogenous cathelicidin was dependent on the presence of functional TLR4. These observations provide evidence that cathelicidin antimicrobial peptides mediate an anti-inflammatory response in part by their activity at the membrane.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents</subject><subject>Antimicrobial Cationic Peptides - pharmacology</subject><subject>Cytokines</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - immunology</subject><subject>Dermatitis, Allergic Contact - drug therapy</subject><subject>Dermatitis, Allergic Contact - etiology</subject><subject>Dermatitis, Allergic Contact - prevention & control</subject><subject>Humans</subject><subject>Immunity</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>T-Lymphocytes - immunology</subject><subject>Toll-Like Receptor 4 - immunology</subject><subject>Toll-Like Receptor 4 - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><issn>1365-2567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkclOwzAURS0EgjJ8ARLyClYpnuLEy1JGqRKIYW05tkMNjlNilwq-npQWwY7V25x79XQPAIcYDRli4vTFNc08tH6Ii3JIh7gkYgMMcJ6jjHPEN8EAIUIyXPBiB-zG-IIQ4oiwbbCDC0ILRukAvI5VmlrvtDMuwFFIrnG6ayunPLyzs-SMjfDMt_oVnttgOpechmPrPXyc3DM40sm9q-TaAFUwcOS97Z6XRBuS0gk-2BD7yOc3sg-2auWjPVjfPfB0efE4vs4mt1c349Ek04ySlFWqVBzVAhFecUYN5kjlldGMKZsXphKIk6LmOa81I7iuqRU11aK0hmKhjaB74HjVO-vat7mNSTYu6v5nFWw7j5KXgpZlwf8FschJTkXeg3QF9tPE2NlazjrXqO5DYiSXMuSPDNnLkFQuZfSpo3X9vGqs-c2s1--BkxUwdc_TheusjI3yvsexXCwWf6q-AG1Nlp0</recordid><startdate>20070201</startdate><enddate>20070201</enddate><creator>Di Nardo, Anna</creator><creator>Braff, Marissa H</creator><creator>Taylor, Kristen R</creator><creator>Na, ChangRim</creator><creator>Granstein, Richard D</creator><creator>McInturff, Jamie E</creator><creator>Krutzik, Stephan</creator><creator>Modlin, Robert L</creator><creator>Gallo, Richard L</creator><general>Am Assoc Immnol</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>7T5</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070201</creationdate><title>Cathelicidin Antimicrobial Peptides Block Dendritic Cell TLR4 Activation and Allergic Contact Sensitization</title><author>Di Nardo, Anna ; 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We studied the role of cathelicidin in allergic contact dermatitis, a model requiring dendritic cells of the innate immune response and T cells of the adaptive immune response. Deletion of the murine cathelicidin gene Cnlp enhanced an allergic contact response, whereas local administration of cathelicidin before sensitization inhibited the allergic response. Cathelicidins inhibited TLR4 but not TLR2 mediated induction of dendritic cell maturation and cytokine release, and this inhibition was associated with an alteration of cell membrane function and structure. Further analysis in vivo connected these observations because inhibition of sensitization by exogenous cathelicidin was dependent on the presence of functional TLR4. 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subjects | Animals Anti-Inflammatory Agents Antimicrobial Cationic Peptides - pharmacology Cytokines Dendritic Cells - drug effects Dendritic Cells - immunology Dermatitis, Allergic Contact - drug therapy Dermatitis, Allergic Contact - etiology Dermatitis, Allergic Contact - prevention & control Humans Immunity Mice Mice, Knockout T-Lymphocytes - immunology Toll-Like Receptor 4 - immunology Toll-Like Receptor 4 - metabolism |
title | Cathelicidin Antimicrobial Peptides Block Dendritic Cell TLR4 Activation and Allergic Contact Sensitization |
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