Aged human skin removes UVB-induced pyrimidine dimers from the epidermis more slowly than younger adult skin in vivo
Although many studies have been reported on the repair of ultraviolet light (UV)-induced cyclobutane-type pyrimidine dimers (CPDs) in DNA, the effects of aging on the removal of UV-induced CPDs from the human skin epidermis in vivo remains uncertain. Therefore, we employed immunoblotting and immunoh...
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description | Although many studies have been reported on the repair of ultraviolet light (UV)-induced cyclobutane-type pyrimidine dimers (CPDs) in DNA, the effects of aging on the removal of UV-induced CPDs from the human skin epidermis in vivo remains uncertain. Therefore, we employed immunoblotting and immunohistochemical methods using monoclonal antibodies (TDM-2) to CPDs to study age-related differences in the time required for the in vivo removal of UVB-induced CPDs. The flexure surfaces of the upper arms of five young men were exposed to UVB light at a fluence of 35 and 700 mJ/cm2, and four older men were also irradiated with the same doses of UVB mentioned above. Each area of skin was biopsied before and immediately after irradiation, and at 4, 24 h, 2 and 4 days after irradiation in the younger group; and before and immediately after irradiation, and at 24 h, 4, 7, and 14 days after irradiation in the older group. A total of 108 DNA samples were taken from the epidermis of 108 biopsied specimens. These samples were immunoblotted using TDM-2 and the intensities of the immunoprecipitates were measured by photodensitometer. Our results show that the CPDs had been removed from the epidermis at 4 days after irradiation at either dose in the younger group, and between 7-14 days after irradiation in the aged group. The results of our immunohistochemical studies were consistent with those of our immunoblotting studies, and indicated that basal cells repair CPDs more quickly than prickle cells in the epidermis except the amounts at 24 h after UVB irradiation, and that the CPDs were removed by epidermal turnover after the nucleotide excision repair (NER). Our results showed age-associated decline in the NER in vivo, indicating high risk of UV-associated skin cancer. |
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Therefore, we employed immunoblotting and immunohistochemical methods using monoclonal antibodies (TDM-2) to CPDs to study age-related differences in the time required for the in vivo removal of UVB-induced CPDs. The flexure surfaces of the upper arms of five young men were exposed to UVB light at a fluence of 35 and 700 mJ/cm2, and four older men were also irradiated with the same doses of UVB mentioned above. Each area of skin was biopsied before and immediately after irradiation, and at 4, 24 h, 2 and 4 days after irradiation in the younger group; and before and immediately after irradiation, and at 24 h, 4, 7, and 14 days after irradiation in the older group. A total of 108 DNA samples were taken from the epidermis of 108 biopsied specimens. These samples were immunoblotted using TDM-2 and the intensities of the immunoprecipitates were measured by photodensitometer. Our results show that the CPDs had been removed from the epidermis at 4 days after irradiation at either dose in the younger group, and between 7-14 days after irradiation in the aged group. The results of our immunohistochemical studies were consistent with those of our immunoblotting studies, and indicated that basal cells repair CPDs more quickly than prickle cells in the epidermis except the amounts at 24 h after UVB irradiation, and that the CPDs were removed by epidermal turnover after the nucleotide excision repair (NER). Our results showed age-associated decline in the NER in vivo, indicating high risk of UV-associated skin cancer.</description><identifier>ISSN: 0340-3696</identifier><identifier>EISSN: 1432-069X</identifier><identifier>DOI: 10.1007/s00403-005-0618-0</identifier><identifier>PMID: 16328344</identifier><identifier>CODEN: ADREDL</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adult ; Aged ; Antibodies, Monoclonal - immunology ; Biological and medical sciences ; Biopsy ; Dermatology ; DNA - analysis ; DNA Damage ; DNA Repair ; Dose-Response Relationship, Radiation ; Epidermis - chemistry ; Epidermis - pathology ; Epidermis - physiology ; Epidermis - radiation effects ; Humans ; Immune Tolerance ; Immunoblotting ; Immunohistochemistry ; Immunoprecipitation ; Male ; Medical sciences ; Pyrimidine Dimers - analysis ; Pyrimidine Dimers - immunology ; Pyrimidine Dimers - metabolism ; Skin Aging - physiology ; Time Factors ; Ultraviolet Rays</subject><ispartof>Archives of Dermatological Research, 2006, Vol.297 (7), p.294-302</ispartof><rights>2006 INIST-CNRS</rights><rights>Springer-Verlag 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-1c5303869d2b3ab40e221175046b5f469de89085bcde2e7f4669b213ab84d3a33</citedby><cites>FETCH-LOGICAL-c356t-1c5303869d2b3ab40e221175046b5f469de89085bcde2e7f4669b213ab84d3a33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17379043$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16328344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>YAMADA, Masao</creatorcontrib><creatorcontrib>UDONO, Masako U</creatorcontrib><creatorcontrib>HORI, Makoto</creatorcontrib><creatorcontrib>HIROSE, Ryoji</creatorcontrib><creatorcontrib>SATO, Shinichi</creatorcontrib><creatorcontrib>MORI, Toshio</creatorcontrib><creatorcontrib>NIKAIDO, Osamu</creatorcontrib><title>Aged human skin removes UVB-induced pyrimidine dimers from the epidermis more slowly than younger adult skin in vivo</title><title>Archives of Dermatological Research</title><addtitle>Arch Dermatol Res</addtitle><description>Although many studies have been reported on the repair of ultraviolet light (UV)-induced cyclobutane-type pyrimidine dimers (CPDs) in DNA, the effects of aging on the removal of UV-induced CPDs from the human skin epidermis in vivo remains uncertain. Therefore, we employed immunoblotting and immunohistochemical methods using monoclonal antibodies (TDM-2) to CPDs to study age-related differences in the time required for the in vivo removal of UVB-induced CPDs. The flexure surfaces of the upper arms of five young men were exposed to UVB light at a fluence of 35 and 700 mJ/cm2, and four older men were also irradiated with the same doses of UVB mentioned above. Each area of skin was biopsied before and immediately after irradiation, and at 4, 24 h, 2 and 4 days after irradiation in the younger group; and before and immediately after irradiation, and at 24 h, 4, 7, and 14 days after irradiation in the older group. A total of 108 DNA samples were taken from the epidermis of 108 biopsied specimens. These samples were immunoblotted using TDM-2 and the intensities of the immunoprecipitates were measured by photodensitometer. Our results show that the CPDs had been removed from the epidermis at 4 days after irradiation at either dose in the younger group, and between 7-14 days after irradiation in the aged group. The results of our immunohistochemical studies were consistent with those of our immunoblotting studies, and indicated that basal cells repair CPDs more quickly than prickle cells in the epidermis except the amounts at 24 h after UVB irradiation, and that the CPDs were removed by epidermal turnover after the nucleotide excision repair (NER). Our results showed age-associated decline in the NER in vivo, indicating high risk of UV-associated skin cancer.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Dermatology</subject><subject>DNA - analysis</subject><subject>DNA Damage</subject><subject>DNA Repair</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Epidermis - chemistry</subject><subject>Epidermis - pathology</subject><subject>Epidermis - physiology</subject><subject>Epidermis - radiation effects</subject><subject>Humans</subject><subject>Immune Tolerance</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>Immunoprecipitation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pyrimidine Dimers - analysis</subject><subject>Pyrimidine Dimers - immunology</subject><subject>Pyrimidine Dimers - metabolism</subject><subject>Skin Aging - physiology</subject><subject>Time Factors</subject><subject>Ultraviolet Rays</subject><issn>0340-3696</issn><issn>1432-069X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpFkNtKAzEQhoMoWrQP4I0EwcvVyWFPl7V4AsEbK96F7Ga2je5uarJb6dub0oIhEDLzzR_yEXLJ4JYB5HcBQIJIANIEMlYkcEQmTAoeb-XnMZmAkJCIrMzOyDSEL4grB8khPyVnLBO8EFJOyDBboqGrsdM9Dd-2px47t8FAFx_3ie3NWMf2euttZ43tkRrboQ-08a6jwwoprq1B39lAO-eRhtb9ttvYiXFbN_ZL9FSbsR324XFv7MZdkJNGtwGnh_OcLB4f3ufPyevb08t89prUIs2GhNWpAFFkpeGV0JUE5JyxPAWZVWkjYx2LEoq0qg1yzGMlKyvOIlpII7QQ5-R6n7v27mfEMKgvN_o-Pqk442wXVEaI7aHauxA8Nmodf6v9VjFQO9Nqb1pF02pnWkGcuToEj1WH5n_i4DUCNwdAh1q3jdd9bcM_l4u8BCnEH-kYhgk</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>YAMADA, Masao</creator><creator>UDONO, Masako U</creator><creator>HORI, Makoto</creator><creator>HIROSE, Ryoji</creator><creator>SATO, Shinichi</creator><creator>MORI, Toshio</creator><creator>NIKAIDO, Osamu</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></search><sort><creationdate>2006</creationdate><title>Aged human skin removes UVB-induced pyrimidine dimers from the epidermis more slowly than younger adult skin in vivo</title><author>YAMADA, Masao ; UDONO, Masako U ; HORI, Makoto ; HIROSE, Ryoji ; SATO, Shinichi ; MORI, Toshio ; NIKAIDO, Osamu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-1c5303869d2b3ab40e221175046b5f469de89085bcde2e7f4669b213ab84d3a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Dermatology</topic><topic>DNA - analysis</topic><topic>DNA Damage</topic><topic>DNA Repair</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Epidermis - chemistry</topic><topic>Epidermis - pathology</topic><topic>Epidermis - physiology</topic><topic>Epidermis - radiation effects</topic><topic>Humans</topic><topic>Immune Tolerance</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>Immunoprecipitation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pyrimidine Dimers - analysis</topic><topic>Pyrimidine Dimers - immunology</topic><topic>Pyrimidine Dimers - metabolism</topic><topic>Skin Aging - physiology</topic><topic>Time Factors</topic><topic>Ultraviolet Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YAMADA, Masao</creatorcontrib><creatorcontrib>UDONO, Masako U</creatorcontrib><creatorcontrib>HORI, Makoto</creatorcontrib><creatorcontrib>HIROSE, Ryoji</creatorcontrib><creatorcontrib>SATO, Shinichi</creatorcontrib><creatorcontrib>MORI, Toshio</creatorcontrib><creatorcontrib>NIKAIDO, Osamu</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 Edition)</collection><collection>ProQuest Central UK/Ireland</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><jtitle>Archives of Dermatological Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YAMADA, Masao</au><au>UDONO, Masako U</au><au>HORI, Makoto</au><au>HIROSE, Ryoji</au><au>SATO, Shinichi</au><au>MORI, Toshio</au><au>NIKAIDO, Osamu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aged human skin removes UVB-induced pyrimidine dimers from the epidermis more slowly than younger adult skin in vivo</atitle><jtitle>Archives of Dermatological Research</jtitle><addtitle>Arch Dermatol Res</addtitle><date>2006</date><risdate>2006</risdate><volume>297</volume><issue>7</issue><spage>294</spage><epage>302</epage><pages>294-302</pages><issn>0340-3696</issn><eissn>1432-069X</eissn><coden>ADREDL</coden><abstract>Although many studies have been reported on the repair of ultraviolet light (UV)-induced cyclobutane-type pyrimidine dimers (CPDs) in DNA, the effects of aging on the removal of UV-induced CPDs from the human skin epidermis in vivo remains uncertain. Therefore, we employed immunoblotting and immunohistochemical methods using monoclonal antibodies (TDM-2) to CPDs to study age-related differences in the time required for the in vivo removal of UVB-induced CPDs. The flexure surfaces of the upper arms of five young men were exposed to UVB light at a fluence of 35 and 700 mJ/cm2, and four older men were also irradiated with the same doses of UVB mentioned above. Each area of skin was biopsied before and immediately after irradiation, and at 4, 24 h, 2 and 4 days after irradiation in the younger group; and before and immediately after irradiation, and at 24 h, 4, 7, and 14 days after irradiation in the older group. A total of 108 DNA samples were taken from the epidermis of 108 biopsied specimens. These samples were immunoblotted using TDM-2 and the intensities of the immunoprecipitates were measured by photodensitometer. Our results show that the CPDs had been removed from the epidermis at 4 days after irradiation at either dose in the younger group, and between 7-14 days after irradiation in the aged group. The results of our immunohistochemical studies were consistent with those of our immunoblotting studies, and indicated that basal cells repair CPDs more quickly than prickle cells in the epidermis except the amounts at 24 h after UVB irradiation, and that the CPDs were removed by epidermal turnover after the nucleotide excision repair (NER). Our results showed age-associated decline in the NER in vivo, indicating high risk of UV-associated skin cancer.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>16328344</pmid><doi>10.1007/s00403-005-0618-0</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Antibodies, Monoclonal - immunology Biological and medical sciences Biopsy Dermatology DNA - analysis DNA Damage DNA Repair Dose-Response Relationship, Radiation Epidermis - chemistry Epidermis - pathology Epidermis - physiology Epidermis - radiation effects Humans Immune Tolerance Immunoblotting Immunohistochemistry Immunoprecipitation Male Medical sciences Pyrimidine Dimers - analysis Pyrimidine Dimers - immunology Pyrimidine Dimers - metabolism Skin Aging - physiology Time Factors Ultraviolet Rays |
title | Aged human skin removes UVB-induced pyrimidine dimers from the epidermis more slowly than younger adult skin in vivo |
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