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
Hauptverfasser: Berneburg, Mark, Plettenberg, Heidi, Medve-König, Kathrin, Pfahlberg, Annette, Gers-Barlag, H., Gefeller, Olaf, Krutmann, Jean
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container_issue 5
container_start_page 1277
container_title Journal of investigative dermatology
container_volume 122
creator Berneburg, Mark
Plettenberg, Heidi
Medve-König, Kathrin
Pfahlberg, Annette
Gers-Barlag, H.
Gefeller, Olaf
Krutmann, Jean
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.
doi_str_mv 10.1111/j.0022-202X.2004.22502.x
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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. 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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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