Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.

BACKGROUND:Exposure to high doses of ionizing radiation (IR) can lead to localized radiation injury of the skin and exposed cells suffer dsDNA breaks that may elicit cell death or stochastic changes. Little is known about the DNA damage response after high-dose exposure of the skin. Here, we investi...

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Main Authors: Emad A Ahmed, Diane Agay, Gerrit Schrock, Michel Drouet, Viktor Meineke, Harry Scherthan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3384646?pdf=render
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spelling doaj-4a479bf7b2df44b19ff95f9877dbbca82020-11-24T21:35:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0176e3952110.1371/journal.pone.0039521Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.Emad A AhmedDiane AgayGerrit SchrockMichel DrouetViktor MeinekeHarry ScherthanBACKGROUND:Exposure to high doses of ionizing radiation (IR) can lead to localized radiation injury of the skin and exposed cells suffer dsDNA breaks that may elicit cell death or stochastic changes. Little is known about the DNA damage response after high-dose exposure of the skin. Here, we investigate the cellular and DNA damage response in acutely irradiated minipig skin. METHODS AND FINDINGS:IR-induced DNA damage, repair and cellular survival were studied in 15 cm(2) of minipig skin exposed in vivo to ~50 Co-60 γ rays. Skin biopsies of control and 4 h up to 96 days post exposure were investigated for radiation-induced foci (RIF) formation using γ-H2AX, 53BP1, and active ATM-p immunofluorescence. High-dose IR induced massive γ-H2AX phosphorylation and high 53BP1 RIF numbers 4 h, 20 h after IR. As time progressed RIF numbers dropped to a low of <1% of keratinocytes at 28-70 days. The latter contained large RIFs that included ATM-p, indicating the accumulation of complex DNA damage. At 96 days most of the cells with RIFs had disappeared. The frequency of active-caspase-3-positive apoptotic cells was 17-fold increased 3 days after IR and remained >3-fold elevated at all subsequent time points. Replicating basal cells (Ki67+) were reduced 3 days post IR followed by increased proliferation and recovery of epidermal cellularity after 28 days. CONCLUSIONS:Acute high dose irradiation of minipig epidermis impaired stem cell replication and induced elevated apoptosis from 3 days onward. DNA repair cleared the high numbers of DBSs in skin cells, while RIFs that persisted in <1% cells marked complex and potentially lethal DNA damage up to several weeks after exposure. An elevated frequency of keratinocytes with persistent RIFs may thus serve as indicator of previous acute radiation exposure, which may be useful in the follow up of nuclear or radiological accident scenarios.http://europepmc.org/articles/PMC3384646?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Emad A Ahmed
Diane Agay
Gerrit Schrock
Michel Drouet
Viktor Meineke
Harry Scherthan
spellingShingle Emad A Ahmed
Diane Agay
Gerrit Schrock
Michel Drouet
Viktor Meineke
Harry Scherthan
Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.
PLoS ONE
author_facet Emad A Ahmed
Diane Agay
Gerrit Schrock
Michel Drouet
Viktor Meineke
Harry Scherthan
author_sort Emad A Ahmed
title Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.
title_short Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.
title_full Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.
title_fullStr Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.
title_full_unstemmed Persistent DNA damage after high dose in vivo gamma exposure of minipig skin.
title_sort persistent dna damage after high dose in vivo gamma exposure of minipig skin.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description BACKGROUND:Exposure to high doses of ionizing radiation (IR) can lead to localized radiation injury of the skin and exposed cells suffer dsDNA breaks that may elicit cell death or stochastic changes. Little is known about the DNA damage response after high-dose exposure of the skin. Here, we investigate the cellular and DNA damage response in acutely irradiated minipig skin. METHODS AND FINDINGS:IR-induced DNA damage, repair and cellular survival were studied in 15 cm(2) of minipig skin exposed in vivo to ~50 Co-60 γ rays. Skin biopsies of control and 4 h up to 96 days post exposure were investigated for radiation-induced foci (RIF) formation using γ-H2AX, 53BP1, and active ATM-p immunofluorescence. High-dose IR induced massive γ-H2AX phosphorylation and high 53BP1 RIF numbers 4 h, 20 h after IR. As time progressed RIF numbers dropped to a low of <1% of keratinocytes at 28-70 days. The latter contained large RIFs that included ATM-p, indicating the accumulation of complex DNA damage. At 96 days most of the cells with RIFs had disappeared. The frequency of active-caspase-3-positive apoptotic cells was 17-fold increased 3 days after IR and remained >3-fold elevated at all subsequent time points. Replicating basal cells (Ki67+) were reduced 3 days post IR followed by increased proliferation and recovery of epidermal cellularity after 28 days. CONCLUSIONS:Acute high dose irradiation of minipig epidermis impaired stem cell replication and induced elevated apoptosis from 3 days onward. DNA repair cleared the high numbers of DBSs in skin cells, while RIFs that persisted in <1% cells marked complex and potentially lethal DNA damage up to several weeks after exposure. An elevated frequency of keratinocytes with persistent RIFs may thus serve as indicator of previous acute radiation exposure, which may be useful in the follow up of nuclear or radiological accident scenarios.
url http://europepmc.org/articles/PMC3384646?pdf=render
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