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C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes
Psoriasis is a chronic, relapsing inflammatory skin disease. The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated th...
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Published in: | Scientific reports 2018-06, Vol.8 (1), p.8590-11, Article 8590 |
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description | Psoriasis is a chronic, relapsing inflammatory skin disease. The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated the functional roles of C10orf99 in epidermal proliferation under inflammatory condition. We showed that C10orf99 protein was significantly up-regulated in psoriatic skin samples from patients and the ortholog gene expression levels were up-regulated in imiquimod (IMQ)-induced psoriasis-like skin lesions in mice. Using M5-stimulated HaCaT cell line model of inflammation and a combinational approach of knockdown and overexpression of C10orf99, we demonstrated that C10orf99 could promote keratinocyte proliferation by facilitating the G1/S transition, and the pro-proliferation effect of C10orf99 was associated with the activation of the ERK1/2 and NF-κB but not the AKT pathways. Local depletion of C10orf99 by lentiviral vectors expressing C10orf99 shRNA effectively ameliorated IMQ-induced dermatitis. Taken together, these results indicate that C10orf99 plays a contributive role in psoriasis pathogenesis and may serve as a new target for psoriasis treatment. |
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The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated the functional roles of C10orf99 in epidermal proliferation under inflammatory condition. We showed that C10orf99 protein was significantly up-regulated in psoriatic skin samples from patients and the ortholog gene expression levels were up-regulated in imiquimod (IMQ)-induced psoriasis-like skin lesions in mice. Using M5-stimulated HaCaT cell line model of inflammation and a combinational approach of knockdown and overexpression of C10orf99, we demonstrated that C10orf99 could promote keratinocyte proliferation by facilitating the G1/S transition, and the pro-proliferation effect of C10orf99 was associated with the activation of the ERK1/2 and NF-κB but not the AKT pathways. Local depletion of C10orf99 by lentiviral vectors expressing C10orf99 shRNA effectively ameliorated IMQ-induced dermatitis. Taken together, these results indicate that C10orf99 plays a contributive role in psoriasis pathogenesis and may serve as a new target for psoriasis treatment.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-26996-z</identifier><identifier>PMID: 29872130</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13 ; 13/109 ; 13/2 ; 13/21 ; 13/31 ; 13/51 ; 13/89 ; 13/95 ; 631/250/249/1313/1758 ; 64/60 ; 692/699/4033 ; AKT protein ; Dermatitis ; Gene expression ; Humanities and Social Sciences ; Imiquimod ; Keratinocytes ; multidisciplinary ; NF-κB protein ; Pathogenesis ; Psoriasis ; Science ; Science (multidisciplinary) ; Skin diseases</subject><ispartof>Scientific reports, 2018-06, Vol.8 (1), p.8590-11, Article 8590</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-7c49d67a8d403eaf4d1232aca477a5c93325192f6a212ceea20494f2c5237e7c3</citedby><cites>FETCH-LOGICAL-c540t-7c49d67a8d403eaf4d1232aca477a5c93325192f6a212ceea20494f2c5237e7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2050462978/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2050462978?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29872130$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Caifeng</creatorcontrib><creatorcontrib>Wu, Na</creatorcontrib><creatorcontrib>Duan, Qiqi</creatorcontrib><creatorcontrib>Yang, Huizi</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Yang, Peiwen</creatorcontrib><creatorcontrib>Zhang, Mengdi</creatorcontrib><creatorcontrib>Liu, Jiankang</creatorcontrib><creatorcontrib>Liu, Zhi</creatorcontrib><creatorcontrib>Shao, Yongping</creatorcontrib><creatorcontrib>Zheng, Yan</creatorcontrib><title>C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Psoriasis is a chronic, relapsing inflammatory skin disease. The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated the functional roles of C10orf99 in epidermal proliferation under inflammatory condition. We showed that C10orf99 protein was significantly up-regulated in psoriatic skin samples from patients and the ortholog gene expression levels were up-regulated in imiquimod (IMQ)-induced psoriasis-like skin lesions in mice. Using M5-stimulated HaCaT cell line model of inflammation and a combinational approach of knockdown and overexpression of C10orf99, we demonstrated that C10orf99 could promote keratinocyte proliferation by facilitating the G1/S transition, and the pro-proliferation effect of C10orf99 was associated with the activation of the ERK1/2 and NF-κB but not the AKT pathways. Local depletion of C10orf99 by lentiviral vectors expressing C10orf99 shRNA effectively ameliorated IMQ-induced dermatitis. Taken together, these results indicate that C10orf99 plays a contributive role in psoriasis pathogenesis and may serve as a new target for psoriasis treatment.</description><subject>13</subject><subject>13/109</subject><subject>13/2</subject><subject>13/21</subject><subject>13/31</subject><subject>13/51</subject><subject>13/89</subject><subject>13/95</subject><subject>631/250/249/1313/1758</subject><subject>64/60</subject><subject>692/699/4033</subject><subject>AKT protein</subject><subject>Dermatitis</subject><subject>Gene expression</subject><subject>Humanities and Social Sciences</subject><subject>Imiquimod</subject><subject>Keratinocytes</subject><subject>multidisciplinary</subject><subject>NF-κB protein</subject><subject>Pathogenesis</subject><subject>Psoriasis</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Skin diseases</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kcFu1DAQhi0EolXpC_SAInHhkmKPnTi-IKFVgUqVeoGz5XUmW5fEDrZTafv0eHfbUjjUF4813_yemZ-QM0bPGeXdpyRYo7qasq6GVqm2vn9FjoGKpgYO8PpZfEROU7ql5TSgBFNvyRGoTgLj9Jj0K0ZDHJSqbPA5uvWSMVU5VPkGqx7vcAzzhD5XYajmFKIzyaVqva3mGKaQnd_syfIa3YDRZBf8jv21j32w26L3jrwZzJjw9OE-IT-_XvxYfa-vrr9drr5c1bYRNNfSCtW30nS9oBzNIHpW-jfWCClNYxXn0DAFQ2uAgUU0ZUQlBrANcInS8hPy-aA7L-sJe1v6jmbUc3STiVsdjNP_Zry70Ztwp8smy0KgCHx8EIjh94Ip68kli-NoPIYlaaANo7J01xX0w3_obViiL-PtKCpaUHJHwYGyMaQUcXhqhlG981EffNTFR733Ud-XovfPx3gqeXStAPwApJLyG4x__35B9g_qN6rf</recordid><startdate>20180605</startdate><enddate>20180605</enddate><creator>Chen, Caifeng</creator><creator>Wu, Na</creator><creator>Duan, Qiqi</creator><creator>Yang, Huizi</creator><creator>Wang, Xin</creator><creator>Yang, Peiwen</creator><creator>Zhang, Mengdi</creator><creator>Liu, Jiankang</creator><creator>Liu, Zhi</creator><creator>Shao, Yongping</creator><creator>Zheng, Yan</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180605</creationdate><title>C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes</title><author>Chen, Caifeng ; 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The pathogenesis of psoriasis is complex and has not been fully understood. C10orf99 was a recently identified human antimicrobial peptide whose mRNA expression is elevated in psoriatic human skin samples. In this study, we investigated the functional roles of C10orf99 in epidermal proliferation under inflammatory condition. We showed that C10orf99 protein was significantly up-regulated in psoriatic skin samples from patients and the ortholog gene expression levels were up-regulated in imiquimod (IMQ)-induced psoriasis-like skin lesions in mice. Using M5-stimulated HaCaT cell line model of inflammation and a combinational approach of knockdown and overexpression of C10orf99, we demonstrated that C10orf99 could promote keratinocyte proliferation by facilitating the G1/S transition, and the pro-proliferation effect of C10orf99 was associated with the activation of the ERK1/2 and NF-κB but not the AKT pathways. Local depletion of C10orf99 by lentiviral vectors expressing C10orf99 shRNA effectively ameliorated IMQ-induced dermatitis. Taken together, these results indicate that C10orf99 plays a contributive role in psoriasis pathogenesis and may serve as a new target for psoriasis treatment.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29872130</pmid><doi>10.1038/s41598-018-26996-z</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13 13/109 13/2 13/21 13/31 13/51 13/89 13/95 631/250/249/1313/1758 64/60 692/699/4033 AKT protein Dermatitis Gene expression Humanities and Social Sciences Imiquimod Keratinocytes multidisciplinary NF-κB protein Pathogenesis Psoriasis Science Science (multidisciplinary) Skin diseases |
title | C10orf99 contributes to the development of psoriasis by promoting the proliferation of keratinocytes |
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