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Upregulation of histidine decarboxylase mRNA expression in scleroderma skin
The involvement of histamine in the pathogenesis of systemic sclerosis (SSc) has been suggested. Possible involvement of histamine and histidine decarboxylase (HDC), the synthesizing enzyme for histamine, in the formation of the skin abnormalities in SSc was studied. Skin histamine concentrations in...
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Published in: | Archives of Dermatological Research 2001-04, Vol.293 (4), p.171-177 |
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container_title | Archives of Dermatological Research |
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creator | OHTSUKA, Tsutomu OHTAKE, Hideki MATSUZAKI, Shigeru ICHIMURA, Kaoru ICHIKAWA, Atsushi YAMAKAGE, Akio YAMAZAKI, Soji |
description | The involvement of histamine in the pathogenesis of systemic sclerosis (SSc) has been suggested. Possible involvement of histamine and histidine decarboxylase (HDC), the synthesizing enzyme for histamine, in the formation of the skin abnormalities in SSc was studied. Skin histamine concentrations in SSc were significantly lower than in normal controls (P < 0.02). In situ hybridization with an HDC probe revealed that the expression of the HDC gene in SSc was greater than in normal controls. The number of cells and the mean grain number per cell expressing HDC mRNA were both significantly greater in SSc than in normal controls (both P < 0.01). These results show a reduction in histamine concentration and an elevated HDC gene expression in SSc skin, indicating an increase in both histamine release and HDC gene expression. The upregulation of histamine turnover appears to be involved in the formation of the skin abnormalities of SSc. |
doi_str_mv | 10.1007/s004030100206 |
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Possible involvement of histamine and histidine decarboxylase (HDC), the synthesizing enzyme for histamine, in the formation of the skin abnormalities in SSc was studied. Skin histamine concentrations in SSc were significantly lower than in normal controls (P < 0.02). In situ hybridization with an HDC probe revealed that the expression of the HDC gene in SSc was greater than in normal controls. The number of cells and the mean grain number per cell expressing HDC mRNA were both significantly greater in SSc than in normal controls (both P < 0.01). These results show a reduction in histamine concentration and an elevated HDC gene expression in SSc skin, indicating an increase in both histamine release and HDC gene expression. The upregulation of histamine turnover appears to be involved in the formation of the skin abnormalities of SSc.</description><identifier>ISSN: 0340-3696</identifier><identifier>EISSN: 1432-069X</identifier><identifier>DOI: 10.1007/s004030100206</identifier><identifier>PMID: 11380149</identifier><identifier>CODEN: ADREDL</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adult ; Biological and medical sciences ; Blotting, Northern ; Female ; Gene Expression ; Histamine ; Histamine - metabolism ; Histidine ; Histidine decarboxylase ; Histidine Decarboxylase - genetics ; Humans ; Hybridization ; In Situ Hybridization ; Male ; Medical sciences ; Middle Aged ; Osmolar Concentration ; RNA, Messenger - metabolism ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Scleroderma ; Scleroderma, Systemic - metabolism ; Scleroderma, Systemic - physiopathology ; Skin ; Skin - metabolism ; Systemic sclerosis ; Tissue Distribution ; Up-Regulation</subject><ispartof>Archives of Dermatological Research, 2001-04, Vol.293 (4), p.171-177</ispartof><rights>2001 INIST-CNRS</rights><rights>Archives of Dermatological Research is a copyright of Springer, (2001). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c346t-a05666fddeb9e5dae20891fc7551da675008e07dfcfe742b2e8d8425c92449aa3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1003968$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11380149$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OHTSUKA, Tsutomu</creatorcontrib><creatorcontrib>OHTAKE, Hideki</creatorcontrib><creatorcontrib>MATSUZAKI, Shigeru</creatorcontrib><creatorcontrib>ICHIMURA, Kaoru</creatorcontrib><creatorcontrib>ICHIKAWA, Atsushi</creatorcontrib><creatorcontrib>YAMAKAGE, Akio</creatorcontrib><creatorcontrib>YAMAZAKI, Soji</creatorcontrib><title>Upregulation of histidine decarboxylase mRNA expression in scleroderma skin</title><title>Archives of Dermatological Research</title><addtitle>Arch Dermatol Res</addtitle><description>The involvement of histamine in the pathogenesis of systemic sclerosis (SSc) has been suggested. Possible involvement of histamine and histidine decarboxylase (HDC), the synthesizing enzyme for histamine, in the formation of the skin abnormalities in SSc was studied. Skin histamine concentrations in SSc were significantly lower than in normal controls (P < 0.02). In situ hybridization with an HDC probe revealed that the expression of the HDC gene in SSc was greater than in normal controls. The number of cells and the mean grain number per cell expressing HDC mRNA were both significantly greater in SSc than in normal controls (both P < 0.01). These results show a reduction in histamine concentration and an elevated HDC gene expression in SSc skin, indicating an increase in both histamine release and HDC gene expression. The upregulation of histamine turnover appears to be involved in the formation of the skin abnormalities of SSc.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Histamine</subject><subject>Histamine - metabolism</subject><subject>Histidine</subject><subject>Histidine decarboxylase</subject><subject>Histidine Decarboxylase - genetics</subject><subject>Humans</subject><subject>Hybridization</subject><subject>In Situ Hybridization</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Osmolar Concentration</subject><subject>RNA, Messenger - metabolism</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Scleroderma</subject><subject>Scleroderma, Systemic - metabolism</subject><subject>Scleroderma, Systemic - physiopathology</subject><subject>Skin</subject><subject>Skin - metabolism</subject><subject>Systemic sclerosis</subject><subject>Tissue Distribution</subject><subject>Up-Regulation</subject><issn>0340-3696</issn><issn>1432-069X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpd0MtLHEEQBvAmKHHRPeYaBiK5TVL9mH4cRXyhRJAs5Db0dtdom3msXTug_31aXEhMXaoOPz6Kj7FPHL5xAPOdABRIKLcA_YEtuJKiBu1-7bEFSAW11E4fsCXRI5QxoASYj-yAc2mBK7dg16tNxvu599s0jdXUVQ-JtimmEauIwef19PzSe8JquPtxUuFz0USvNI0VhR7zFDEPvqLfaTxi-53vCZe7fchW52c_Ty_rm9uLq9OTmzpIpbe1h0Zr3cWIa4dN9CjAOt4F0zQ8em0aAItgYhc6NEqsBdpolWiCE0o57-Uh-_qWu8nT04y0bYdEAfvejzjN1BpwpRHbFPjlP_g4zXksv7VCWNDCaqOLqt9UyBNRxq7d5DT4_NJyaF9rbt_VXPznXeq8HjD-1btSCzjeAU_B9132Y0j0TypIp638A-6Pg4I</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>OHTSUKA, Tsutomu</creator><creator>OHTAKE, Hideki</creator><creator>MATSUZAKI, Shigeru</creator><creator>ICHIMURA, Kaoru</creator><creator>ICHIKAWA, Atsushi</creator><creator>YAMAKAGE, Akio</creator><creator>YAMAZAKI, Soji</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20010401</creationdate><title>Upregulation of histidine decarboxylase mRNA expression in scleroderma skin</title><author>OHTSUKA, Tsutomu ; OHTAKE, Hideki ; MATSUZAKI, Shigeru ; ICHIMURA, Kaoru ; ICHIKAWA, Atsushi ; YAMAKAGE, Akio ; YAMAZAKI, Soji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c346t-a05666fddeb9e5dae20891fc7551da675008e07dfcfe742b2e8d8425c92449aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Histamine</topic><topic>Histamine - metabolism</topic><topic>Histidine</topic><topic>Histidine decarboxylase</topic><topic>Histidine Decarboxylase - genetics</topic><topic>Humans</topic><topic>Hybridization</topic><topic>In Situ Hybridization</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Osmolar Concentration</topic><topic>RNA, Messenger - metabolism</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Scleroderma</topic><topic>Scleroderma, Systemic - metabolism</topic><topic>Scleroderma, Systemic - physiopathology</topic><topic>Skin</topic><topic>Skin - metabolism</topic><topic>Systemic sclerosis</topic><topic>Tissue Distribution</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OHTSUKA, Tsutomu</creatorcontrib><creatorcontrib>OHTAKE, Hideki</creatorcontrib><creatorcontrib>MATSUZAKI, Shigeru</creatorcontrib><creatorcontrib>ICHIMURA, Kaoru</creatorcontrib><creatorcontrib>ICHIKAWA, Atsushi</creatorcontrib><creatorcontrib>YAMAKAGE, Akio</creatorcontrib><creatorcontrib>YAMAZAKI, Soji</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of Dermatological Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OHTSUKA, Tsutomu</au><au>OHTAKE, Hideki</au><au>MATSUZAKI, Shigeru</au><au>ICHIMURA, Kaoru</au><au>ICHIKAWA, Atsushi</au><au>YAMAKAGE, Akio</au><au>YAMAZAKI, Soji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Upregulation of histidine decarboxylase mRNA expression in scleroderma skin</atitle><jtitle>Archives of Dermatological Research</jtitle><addtitle>Arch Dermatol Res</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>293</volume><issue>4</issue><spage>171</spage><epage>177</epage><pages>171-177</pages><issn>0340-3696</issn><eissn>1432-069X</eissn><coden>ADREDL</coden><abstract>The involvement of histamine in the pathogenesis of systemic sclerosis (SSc) has been suggested. Possible involvement of histamine and histidine decarboxylase (HDC), the synthesizing enzyme for histamine, in the formation of the skin abnormalities in SSc was studied. Skin histamine concentrations in SSc were significantly lower than in normal controls (P < 0.02). In situ hybridization with an HDC probe revealed that the expression of the HDC gene in SSc was greater than in normal controls. The number of cells and the mean grain number per cell expressing HDC mRNA were both significantly greater in SSc than in normal controls (both P < 0.01). These results show a reduction in histamine concentration and an elevated HDC gene expression in SSc skin, indicating an increase in both histamine release and HDC gene expression. The upregulation of histamine turnover appears to be involved in the formation of the skin abnormalities of SSc.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>11380149</pmid><doi>10.1007/s004030100206</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Blotting, Northern Female Gene Expression Histamine Histamine - metabolism Histidine Histidine decarboxylase Histidine Decarboxylase - genetics Humans Hybridization In Situ Hybridization Male Medical sciences Middle Aged Osmolar Concentration RNA, Messenger - metabolism Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Scleroderma Scleroderma, Systemic - metabolism Scleroderma, Systemic - physiopathology Skin Skin - metabolism Systemic sclerosis Tissue Distribution Up-Regulation |
title | Upregulation of histidine decarboxylase mRNA expression in scleroderma skin |
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