IL-6 EXPRESSION BY ORAL FIBROBLASTS IS REGULATED BY ANDROGEN
Interleukin 6 (IL-6) is a multi-functional cytokine which has a major role in tissue damage. It is secreted by many types of cell, including oral fibroblasts, and has been implicated in the pathogenesis of periodontal diseases particularly those associated with sex hormones. In the present study we...
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Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 1998-08, Vol.10 (8), p.613-619 |
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description | Interleukin 6 (IL-6) is a multi-functional cytokine which has a major role in tissue damage. It is secreted by many types of cell, including oral fibroblasts, and has been implicated in the pathogenesis of periodontal diseases particularly those associated with sex hormones. In the present study we investigate whether the androgen dihydrotestosterone (DHT) affects the expression and regulation of IL-6 in gingival fibroblasts. Using a ‘capture’ ELISA assay, it was found that decreasing DHT concentrations progressively reduced IL-6 production by gingival cells from normal individuals and from patients with gingival inflammation and gingival hyperplasia. In contrast, cells from periodontal ligament tissue produced only barely detectable levels of IL-6. The anti-androgen cyproterone acetate acted as an androgen analogue in the gingival fibroblast, potently inhibiting IL-6 production, and did not reverse the DHT-mediated downregulation of the cytokine. Flutamide also failed to abrogate DHT inhibition of IL-6 production, and it had no effect on IL-6 production in the absence of DHT. Moveover, semi-quantitative RT-PCR showed that DHT acted at the level of transcription of the IL-6 gene, causing a marked reduction in the relative level of IL-6 mRNA in gingival cells. |
doi_str_mv | 10.1006/cyto.1998.0336 |
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It is secreted by many types of cell, including oral fibroblasts, and has been implicated in the pathogenesis of periodontal diseases particularly those associated with sex hormones. In the present study we investigate whether the androgen dihydrotestosterone (DHT) affects the expression and regulation of IL-6 in gingival fibroblasts. Using a ‘capture’ ELISA assay, it was found that decreasing DHT concentrations progressively reduced IL-6 production by gingival cells from normal individuals and from patients with gingival inflammation and gingival hyperplasia. In contrast, cells from periodontal ligament tissue produced only barely detectable levels of IL-6. The anti-androgen cyproterone acetate acted as an androgen analogue in the gingival fibroblast, potently inhibiting IL-6 production, and did not reverse the DHT-mediated downregulation of the cytokine. Flutamide also failed to abrogate DHT inhibition of IL-6 production, and it had no effect on IL-6 production in the absence of DHT. Moveover, semi-quantitative RT-PCR showed that DHT acted at the level of transcription of the IL-6 gene, causing a marked reduction in the relative level of IL-6 mRNA in gingival cells.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1006/cyto.1998.0336</identifier><identifier>PMID: 9722934</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>androgen ; Androgen Antagonists - pharmacology ; Cells, Cultured ; Cyproterone Acetate - pharmacology ; Dihydrotestosterone - metabolism ; Dihydrotestosterone - pharmacology ; fibroblasts ; Fibroblasts - cytology ; Fibroblasts - drug effects ; Fibroblasts - metabolism ; Flutamide - pharmacology ; Gene Expression Regulation ; Gingiva - cytology ; Gingiva - metabolism ; Humans ; IL-6 ; Interleukin-6 - biosynthesis ; oral ; regulation</subject><ispartof>Cytokine (Philadelphia, Pa.), 1998-08, Vol.10 (8), p.613-619</ispartof><rights>1998 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-e3c7bbab00bdd41fc2fa2a85ea6be831722388c262a4c440f091399c53adabbc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/cyto.1998.0336$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9722934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parkar, Mohamed</creatorcontrib><creatorcontrib>Tabona, Peter</creatorcontrib><creatorcontrib>Newman, Hubert</creatorcontrib><creatorcontrib>Olsen, Irwin</creatorcontrib><title>IL-6 EXPRESSION BY ORAL FIBROBLASTS IS REGULATED BY ANDROGEN</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>Interleukin 6 (IL-6) is a multi-functional cytokine which has a major role in tissue damage. It is secreted by many types of cell, including oral fibroblasts, and has been implicated in the pathogenesis of periodontal diseases particularly those associated with sex hormones. In the present study we investigate whether the androgen dihydrotestosterone (DHT) affects the expression and regulation of IL-6 in gingival fibroblasts. Using a ‘capture’ ELISA assay, it was found that decreasing DHT concentrations progressively reduced IL-6 production by gingival cells from normal individuals and from patients with gingival inflammation and gingival hyperplasia. In contrast, cells from periodontal ligament tissue produced only barely detectable levels of IL-6. The anti-androgen cyproterone acetate acted as an androgen analogue in the gingival fibroblast, potently inhibiting IL-6 production, and did not reverse the DHT-mediated downregulation of the cytokine. Flutamide also failed to abrogate DHT inhibition of IL-6 production, and it had no effect on IL-6 production in the absence of DHT. Moveover, semi-quantitative RT-PCR showed that DHT acted at the level of transcription of the IL-6 gene, causing a marked reduction in the relative level of IL-6 mRNA in gingival cells.</description><subject>androgen</subject><subject>Androgen Antagonists - pharmacology</subject><subject>Cells, Cultured</subject><subject>Cyproterone Acetate - pharmacology</subject><subject>Dihydrotestosterone - metabolism</subject><subject>Dihydrotestosterone - pharmacology</subject><subject>fibroblasts</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - metabolism</subject><subject>Flutamide - pharmacology</subject><subject>Gene Expression Regulation</subject><subject>Gingiva - cytology</subject><subject>Gingiva - metabolism</subject><subject>Humans</subject><subject>IL-6</subject><subject>Interleukin-6 - biosynthesis</subject><subject>oral</subject><subject>regulation</subject><issn>1043-4666</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFLwzAUh4Moc06v3oSevLW-NF2agJdu62ahrNJuoKeQpClUtnU2m7D_3pYNb57eg_e9H-99CD1i8DAAfdGnQ-NhzpkHhNArNMTAqQvgk-u-D4gbUEpv0Z21XwDASRgO0ICHvs9JMESvSepSJ_54z-OiSLKlM_l0sjxKnXkyybNJGhWrwkkKJ48X6zRaxbMeiJazPFvEy3t0U8mNNQ-XOkLrebyavrlptkimUepqQvjBNUSHSkkFoMoywJX2K-lLNjaSKsMI7m4hjGmf-jLQQQAVcEw412MiS6mUJiP0fM7dt8330diD2NZWm81G7kxztCIkbMxpyDrQO4O6baxtTSX2bb2V7UlgEL0u0esSvS7R6-oWni7JR7U15R9-8dPN2Xluuvd-atMKq2uz06asW6MPomzq_6J_Aapxc6c</recordid><startdate>19980801</startdate><enddate>19980801</enddate><creator>Parkar, Mohamed</creator><creator>Tabona, Peter</creator><creator>Newman, Hubert</creator><creator>Olsen, Irwin</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>19980801</creationdate><title>IL-6 EXPRESSION BY ORAL FIBROBLASTS IS REGULATED BY ANDROGEN</title><author>Parkar, Mohamed ; Tabona, Peter ; Newman, Hubert ; Olsen, Irwin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-e3c7bbab00bdd41fc2fa2a85ea6be831722388c262a4c440f091399c53adabbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>androgen</topic><topic>Androgen Antagonists - pharmacology</topic><topic>Cells, Cultured</topic><topic>Cyproterone Acetate - pharmacology</topic><topic>Dihydrotestosterone - metabolism</topic><topic>Dihydrotestosterone - pharmacology</topic><topic>fibroblasts</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - metabolism</topic><topic>Flutamide - pharmacology</topic><topic>Gene Expression Regulation</topic><topic>Gingiva - cytology</topic><topic>Gingiva - metabolism</topic><topic>Humans</topic><topic>IL-6</topic><topic>Interleukin-6 - biosynthesis</topic><topic>oral</topic><topic>regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parkar, Mohamed</creatorcontrib><creatorcontrib>Tabona, Peter</creatorcontrib><creatorcontrib>Newman, Hubert</creatorcontrib><creatorcontrib>Olsen, Irwin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parkar, Mohamed</au><au>Tabona, Peter</au><au>Newman, Hubert</au><au>Olsen, Irwin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IL-6 EXPRESSION BY ORAL FIBROBLASTS IS REGULATED BY ANDROGEN</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>1998-08-01</date><risdate>1998</risdate><volume>10</volume><issue>8</issue><spage>613</spage><epage>619</epage><pages>613-619</pages><issn>1043-4666</issn><eissn>1096-0023</eissn><abstract>Interleukin 6 (IL-6) is a multi-functional cytokine which has a major role in tissue damage. It is secreted by many types of cell, including oral fibroblasts, and has been implicated in the pathogenesis of periodontal diseases particularly those associated with sex hormones. In the present study we investigate whether the androgen dihydrotestosterone (DHT) affects the expression and regulation of IL-6 in gingival fibroblasts. Using a ‘capture’ ELISA assay, it was found that decreasing DHT concentrations progressively reduced IL-6 production by gingival cells from normal individuals and from patients with gingival inflammation and gingival hyperplasia. In contrast, cells from periodontal ligament tissue produced only barely detectable levels of IL-6. The anti-androgen cyproterone acetate acted as an androgen analogue in the gingival fibroblast, potently inhibiting IL-6 production, and did not reverse the DHT-mediated downregulation of the cytokine. Flutamide also failed to abrogate DHT inhibition of IL-6 production, and it had no effect on IL-6 production in the absence of DHT. Moveover, semi-quantitative RT-PCR showed that DHT acted at the level of transcription of the IL-6 gene, causing a marked reduction in the relative level of IL-6 mRNA in gingival cells.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>9722934</pmid><doi>10.1006/cyto.1998.0336</doi><tpages>7</tpages></addata></record> |
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subjects | androgen Androgen Antagonists - pharmacology Cells, Cultured Cyproterone Acetate - pharmacology Dihydrotestosterone - metabolism Dihydrotestosterone - pharmacology fibroblasts Fibroblasts - cytology Fibroblasts - drug effects Fibroblasts - metabolism Flutamide - pharmacology Gene Expression Regulation Gingiva - cytology Gingiva - metabolism Humans IL-6 Interleukin-6 - biosynthesis oral regulation |
title | IL-6 EXPRESSION BY ORAL FIBROBLASTS IS REGULATED BY ANDROGEN |
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