Induction of the Photoaging-Associated Mitochondrial Common Deletion In Vivo in Normal Human Skin
Mutations of mitochondrial (mt) DNA such as the 4977 base-pair large-scale deletion, also called common deletion, are increased in photoaged skin. Direct evidence for their induction by chronic exposure to ultraviolet (UV) radiation in vivo in human skin has remained elusive however. Furthermore, th...
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Veröffentlicht in: | Journal of investigative dermatology 2004-05, Vol.122 (5), p.1277-1283 |
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description | Mutations of mitochondrial (mt) DNA such as the 4977 base-pair large-scale deletion, also called common deletion, are increased in photoaged skin. Direct evidence for their induction by chronic exposure to ultraviolet (UV) radiation in vivo in human skin has remained elusive however. Furthermore, their fate after induction is unclear. Previously unirradiated skin of 52 normal human individuals was repetitively exposed to physiological doses of UVA light. Skin and blood specimens were investigated for the presence of mtDNA mutations employing semiquantitative nested PCR, as well as real-time PCR, after 2 weeks of UV exposure and the content of the common deletion was followed up for up to 16 mo after cessation of irradiation. As assessed by both methods, repetitive UV exposure led to an approximately 40% increase in the levels of the common deletion in normal human skin. The majority of deletions were detectable in the dermis also showing the biggest increase, whereas in the epidermis only residual levels and no increase were found. Nine individuals were examined up to 16 mo after cessation of UV exposure and some showed accumulation up to 32-fold. Thus, mtDNA mutations are induced in the human skin by repetitive UV exposure. In addition, these mutations seem to represent long-term in-vivo biomarkers for actinic damage in the human skin. |
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Direct evidence for their induction by chronic exposure to ultraviolet (UV) radiation in vivo in human skin has remained elusive however. Furthermore, their fate after induction is unclear. Previously unirradiated skin of 52 normal human individuals was repetitively exposed to physiological doses of UVA light. Skin and blood specimens were investigated for the presence of mtDNA mutations employing semiquantitative nested PCR, as well as real-time PCR, after 2 weeks of UV exposure and the content of the common deletion was followed up for up to 16 mo after cessation of irradiation. As assessed by both methods, repetitive UV exposure led to an approximately 40% increase in the levels of the common deletion in normal human skin. The majority of deletions were detectable in the dermis also showing the biggest increase, whereas in the epidermis only residual levels and no increase were found. Nine individuals were examined up to 16 mo after cessation of UV exposure and some showed accumulation up to 32-fold. Thus, mtDNA mutations are induced in the human skin by repetitive UV exposure. In addition, these mutations seem to represent long-term in-vivo biomarkers for actinic damage in the human skin.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1111/j.0022-202X.2004.22502.x</identifier><identifier>PMID: 15140232</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; biomarker ; Biomarkers ; Dermis - physiopathology ; Dermis - radiation effects ; DNA, Mitochondrial - genetics ; DNA, Mitochondrial - radiation effects ; Female ; Gene Deletion ; Humans ; Male ; mitochondria ; mitochondrial DNA ; Skin Aging - physiology ; ultraviolet light ; Ultraviolet Rays - adverse effects</subject><ispartof>Journal of investigative dermatology, 2004-05, Vol.122 (5), p.1277-1283</ispartof><rights>2004 The Society for Investigative Dermatology, Inc</rights><rights>Copyright Nature Publishing Group May 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-111538a8b54a1df6b8cfbd7a99b0cd7492f0eff61ebfa33ae0cdbddd1a0bbf473</citedby><cites>FETCH-LOGICAL-c513t-111538a8b54a1df6b8cfbd7a99b0cd7492f0eff61ebfa33ae0cdbddd1a0bbf473</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/15140232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Berneburg, Mark</creatorcontrib><creatorcontrib>Plettenberg, Heidi</creatorcontrib><creatorcontrib>Medve-König, Kathrin</creatorcontrib><creatorcontrib>Pfahlberg, Annette</creatorcontrib><creatorcontrib>Gers-Barlag, H.</creatorcontrib><creatorcontrib>Gefeller, Olaf</creatorcontrib><creatorcontrib>Krutmann, Jean</creatorcontrib><title>Induction of the Photoaging-Associated Mitochondrial Common Deletion In Vivo in Normal Human Skin</title><title>Journal of investigative dermatology</title><addtitle>J Invest Dermatol</addtitle><description>Mutations of mitochondrial (mt) DNA such as the 4977 base-pair large-scale deletion, also called common deletion, are increased in photoaged skin. Direct evidence for their induction by chronic exposure to ultraviolet (UV) radiation in vivo in human skin has remained elusive however. Furthermore, their fate after induction is unclear. Previously unirradiated skin of 52 normal human individuals was repetitively exposed to physiological doses of UVA light. Skin and blood specimens were investigated for the presence of mtDNA mutations employing semiquantitative nested PCR, as well as real-time PCR, after 2 weeks of UV exposure and the content of the common deletion was followed up for up to 16 mo after cessation of irradiation. As assessed by both methods, repetitive UV exposure led to an approximately 40% increase in the levels of the common deletion in normal human skin. The majority of deletions were detectable in the dermis also showing the biggest increase, whereas in the epidermis only residual levels and no increase were found. Nine individuals were examined up to 16 mo after cessation of UV exposure and some showed accumulation up to 32-fold. Thus, mtDNA mutations are induced in the human skin by repetitive UV exposure. In addition, these mutations seem to represent long-term in-vivo biomarkers for actinic damage in the human skin.</description><subject>Adolescent</subject><subject>Adult</subject><subject>biomarker</subject><subject>Biomarkers</subject><subject>Dermis - physiopathology</subject><subject>Dermis - radiation effects</subject><subject>DNA, Mitochondrial - genetics</subject><subject>DNA, Mitochondrial - radiation effects</subject><subject>Female</subject><subject>Gene Deletion</subject><subject>Humans</subject><subject>Male</subject><subject>mitochondria</subject><subject>mitochondrial DNA</subject><subject>Skin Aging - physiology</subject><subject>ultraviolet light</subject><subject>Ultraviolet Rays - adverse effects</subject><issn>0022-202X</issn><issn>1523-1747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkc1O3DAURi1EBQPlFZDFgl1S20kmyZIOtIxEWyQKYmf555rxkNhgJ4i-PQ4zKlI39caSdb5r-3wIYUpymtaXdU4IYxkj7D5nhJQ5YxVh-esOmtGKFRmty3oXzf5C--ggxjUhdF5WzR7apxUtCSvYDIml06MarHfYGzysAF-v_ODFg3UP2VmMXlkxgMY_7ODVyjsdrOjwwvd9SpxDB-_RpcN39sVj6_BPH_pEXI69cPjm0brP6JMRXYSj7X6Ibr9d_F5cZle_vi8XZ1eZqmgxZOlbVdGIRlaloNrMZaOM1LVoW0mUrsuWGQLGzClII4pCQDqVWmsqiJSmrItDdLqZ-xT88whx4L2NCrpOOPBj5DVtk6V2nsCTf8C1H4NLb-OMkqKuWjJBzQZSwccYwPCnYHsR_nBK-NQBX_NJL5_08qkD_t4Bf03R4-38UfagP4Jb6Qn4ugEg6XixEHhUFpwCbQOogWtv_3_LG8SXmYo</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Berneburg, Mark</creator><creator>Plettenberg, Heidi</creator><creator>Medve-König, Kathrin</creator><creator>Pfahlberg, Annette</creator><creator>Gers-Barlag, H.</creator><creator>Gefeller, Olaf</creator><creator>Krutmann, Jean</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20040501</creationdate><title>Induction of the Photoaging-Associated Mitochondrial Common Deletion In Vivo in Normal Human Skin</title><author>Berneburg, Mark ; 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Direct evidence for their induction by chronic exposure to ultraviolet (UV) radiation in vivo in human skin has remained elusive however. Furthermore, their fate after induction is unclear. Previously unirradiated skin of 52 normal human individuals was repetitively exposed to physiological doses of UVA light. Skin and blood specimens were investigated for the presence of mtDNA mutations employing semiquantitative nested PCR, as well as real-time PCR, after 2 weeks of UV exposure and the content of the common deletion was followed up for up to 16 mo after cessation of irradiation. As assessed by both methods, repetitive UV exposure led to an approximately 40% increase in the levels of the common deletion in normal human skin. The majority of deletions were detectable in the dermis also showing the biggest increase, whereas in the epidermis only residual levels and no increase were found. Nine individuals were examined up to 16 mo after cessation of UV exposure and some showed accumulation up to 32-fold. Thus, mtDNA mutations are induced in the human skin by repetitive UV exposure. In addition, these mutations seem to represent long-term in-vivo biomarkers for actinic damage in the human skin.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15140232</pmid><doi>10.1111/j.0022-202X.2004.22502.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult biomarker Biomarkers Dermis - physiopathology Dermis - radiation effects DNA, Mitochondrial - genetics DNA, Mitochondrial - radiation effects Female Gene Deletion Humans Male mitochondria mitochondrial DNA Skin Aging - physiology ultraviolet light Ultraviolet Rays - adverse effects |
title | Induction of the Photoaging-Associated Mitochondrial Common Deletion In Vivo in Normal Human Skin |
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