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Repeated Nrf2 stimulation using sulforaphane protects fibroblasts from ionizing radiation

Mathew, Sherin T (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine
Bergström, Petra (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine
Hammarsten, Ola (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för klinisk kemi och transfusionsmedicin,Institute of Biomedicine, Department of Clinical Chemistry and Transfusion Medicine
 (creator_code:org_t)
Elsevier BV, 2014
2014
Engelska.
Ingår i: Toxicology and Applied Pharmacology. - : Elsevier BV. - 0041-008X. ; 276:3, s. 188-194
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Most of the cytotoxicity induced by ionizing radiation is mediated by radical-induced DNA double-strand breaks. Cellular protection from free radicals can be stimulated several fold by sulforaphane-mediated activation of the transcription factor Nrf2 that regulates more than 50 genes involved in the detoxification of reactive substances and radicals. Here, we report that repeated sulforaphane treatment increases radioresistance in primary human skin fibroblasts. Cells were either treated with sulforaphane for four hours once or with four-hour treatments repeatedly for three consecutive days prior to radiation exposure. Fibroblasts exposed to repeated-sulforaphane treatment showed a more pronounced dose-dependent induction of Nrf2-regulated mRNA and reduced amount of radiation-induced free radicals compared with cells treated once with sulforaphane. In addition, radiation- induced DNA double-strand breaks measured by gamma-H2AX foci were attenuated following repeated sulforaphane treatment. As a result, cellular protection from ionizing radiation measured by the 5-ethynyl-2'-deoxyuridine (EdU) assay was increased, specifically in cells exposed to repeated sulforaphane treatment. Sulforaphane treatment was unable to protect Nrf2 knockout mouse embryonic fibroblasts, indicating that the sulforaphane-induced radioprotection was Nrf2-dependent. Moreover, radioprotection by repeated sulforaphane treatment was dose-dependent with an optimal effect at 10 uM, whereas both lower and higher concentrations resulted in lower levels of radioprotection. Our data indicate that the Nrf2 system can be trained to provide further protection from radical damage. (c) 2014 Elsevier Inc. All rights reserved.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Biomedicinsk laboratorievetenskap/teknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Biomedical Laboratory Science/Technology (hsv//eng)

Nyckelord

Ionizing radiation
Free radicals
Nrf2
Sulforaphane
Cell survival
DNA damage
SMOKE-INDUCED EMPHYSEMA
DOUBLE-STRAND BREAKS
ANTIOXIDANT RESPONSE
INDUCED APOPTOSIS
OXIDATIVE STRESS
GENE-EXPRESSION
FREE-RADICALS
DNA
ENZYMES
MICE
ATES OF AMERICA
V99
P11908
ATES OF AMERICA
V98
P3410

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Av författaren/redakt...
Mathew, Sherin T
Bergström, Petra
Hammarsten, Ola
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MEDICIN OCH HÄLSOVETENSKAP
MEDICIN OCH HÄLS ...
och Medicinsk biotek ...
och Biomedicinsk lab ...
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Toxicology and A ...
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Göteborgs universitet

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