Induction and repair of DNA DSB as revealed by H2AX phosphorylation foci in human fibroblasts exposed to low-and high-LET radiation: Relationship with early and delayed reproductive cell death

TitoloInduction and repair of DNA DSB as revealed by H2AX phosphorylation foci in human fibroblasts exposed to low-and high-LET radiation: Relationship with early and delayed reproductive cell death
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2015
AutoriAntonelli, Francesca, Campa A., Esposito G., Giardullo Paola, Belli M., Dini V., Meschini S., Simone G., Sorrentino E., Gerardi S., Cirrone G.A.P., and Tabocchini M.A.
RivistaRadiation Research
Volume183
Paginazione417-431
ISSN00337587
Parole chiavealpha radiation, article, carbon, cell death, cell killing, Cell Line, Cell Nucleus, controlled study, cytology, DNA Breaks, DNA damage, DNA repair, Dose-Response Relationship, double stranded DNA break, Double-Stranded, fibroblast, Fibroblasts, gamma radiation, histone, histone gamma H2AX, histone H2AX, Histones, human, human cell, Humans, Kinetics, linear energy transfer, metabolism, mutation, nuclear protein, Phosphorylation, priority journal, protein dephosphorylation, protein phosphorylation, proton radiation, Radiation, radiation response, simulation, statistical analysis, unclassified drug
Astratto

The spatial distribution of radiation-induced DNA breaks within the cell nucleus depends on radiation quality in terms of energy deposition pattern. It is generally assumed that the higher the radiation linear energy transfer (LET), the greater the DNA damage complexity. Using a combined experimental and theoretical approach, we examined the phosphorylation-dephosphorylation kinetics of radiation-induced γ-H2AX foci, size distribution and 3D focus morphology, and the relationship between DNA damage and cellular end points (i.e., cell killing and lethal mutations) after exposure to gamma rays, protons, carbon ions and alpha particles. Our results showed that the maximum number of foci are reached 30 min postirradiation for all radiation types. However, the number of foci after 0.5 Gy of each radiation type was different with gamma rays, protons, carbon ions and alpha particles inducing 12.64 ± 0.25, 10.11 ± 0.40, 8.84 ± 0.56 and 4.80 ± 0.35 foci, respectively, which indicated a clear influence of the track structure and fluence on the numbers of foci induced after a dose of 0.5 Gy for each radiation type. The γ-H2AX foci persistence was also dependent on radiation quality, i.e., the higher the LET, the longer the foci persisted in the cell nucleus. The γ-H2AX time course was compared with cell killing and lethal mutation and the results highlighted a correlation between cellular end points and the duration of γ-H2AX foci persistence. A model was developed to evaluate the probability that multiple DSBs reside in the same gamma-ray focus and such probability was found to be negligible for doses lower than 1 Gy. Our model provides evidence that the DSBs inside complex foci, such as those induced by alpha particles, are not processed independently or with the same time constant. The combination of experimental, theoretical and simulation data supports the hypothesis of an interdependent processing of closely associated DSBs, possibly associated with a diminished correct repair capability, which affects cell killing and lethal mutation. © 2015 by Radiation Research Society.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84928575577&doi=10.1667%2fRR13855.1&partnerID=40&md5=882a7ca5249922de5790329c99c1f048
DOI10.1667/RR13855.1