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1000 Titel
  • Effect of cryopreservation on DNA damage and DNA repair activity in human blood samples in the comet assay
1000 Autor/in
  1. Bankoglu, Ezgi Eylül |
  2. Stipp, Franzisca |
  3. Gerber, Johanna |
  4. Seyfried, Florian |
  5. Heidland, August |
  6. Bahner, Udo |
  7. Stopper, Helga |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-03-05
1000 Erschienen in
1000 Quellenangabe
  • 95(5):1831-1841
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00204-021-03012-4 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113209/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • The comet assay is a commonly used method to determine DNA damage and repair activity in many types of samples. In recent years, the use of the comet assay in human biomonitoring became highly attractive due to its various modified versions, which may be useful to determine individual susceptibility in blood samples. However, in human biomonitoring studies, working with large sample numbers that are acquired over an extended time period requires some additional considerations. One of the most important issues is the storage of samples and its effect on the outcome of the comet assay. Another important question is the suitability of different blood preparations. In this study, we analysed the effect of cryopreservation on DNA damage and repair activity in human blood samples. In addition, we investigated the suitability of different blood preparations. The alkaline and FPG as well as two different types of repair comet assay and an in vitro hydrogen peroxide challenge were applied. Our results confirmed that cryopreserved blood preparations are suitable for investigating DNA damage in the alkaline and FPG comet assay in whole blood, buffy coat and PBMCs. Ex vivo hydrogen peroxide challenge yielded its optimal effect in isolated PBMCs. The utilised repair comet assay with either UVC or hydrogen peroxide-induced lesions and an aphidicolin block worked well in fresh PBMCs. Cryopreserved PBMCs could not be used immediately after thawing. However, a 16-h recovery with or without mitotic stimulation enabled the application of the repair comet assay, albeit only in a surviving cell fraction.
1000 Sacherschließung
lokal Leukocytes, Mononuclear [MeSH]
lokal Blood samples
lokal Human biomonitoring
lokal Cryopreservation [MeSH]
lokal DNA Repair [MeSH]
lokal Humans [MeSH]
lokal Genotoxicity and Carcinogenicity
lokal Comet Assay/methods [MeSH]
lokal DNA Damage [MeSH]
lokal Biological Monitoring [MeSH]
lokal DNA damage
lokal Hydrogen Peroxide [MeSH]
lokal Comet assay
lokal DNA repair
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-7488-6228|https://frl.publisso.de/adhoc/uri/U3RpcHAsIEZyYW56aXNjYQ==|https://frl.publisso.de/adhoc/uri/R2VyYmVyLCBKb2hhbm5h|https://frl.publisso.de/adhoc/uri/U2V5ZnJpZWQsIEZsb3JpYW4=|https://frl.publisso.de/adhoc/uri/SGVpZGxhbmQsIEF1Z3VzdA==|https://frl.publisso.de/adhoc/uri/QmFobmVyLCBVZG8=|https://frl.publisso.de/adhoc/uri/U3RvcHBlciwgSGVsZ2E=
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1000 Erstellt am 2023-05-11T14:30:13.865+0200
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