Asian Journal of Andrology · 2008 · 30 citations · 17 references
Life SciencesBiochemistryMolecular BiologyChemotherapyDna RepairReproductive BiologyDna Damage SignalingSperm BiologySperm Dna Integrity AssessmentApoptosis In SpermComet Assay ScoringDna Double-strand BreaksDouble-strand Dna BreaksLesion-specific Dna Repair ProteinsNeutral Comet AssaySperm Chromatin Structure AssaySperm Dna Damage
AIM: To investigate whether adriamycin induces DNA damage and the formation of gammaH2AX (the phosphorylated form of histone H2AX) foci in mature spermatozoa. METHODS: Human spermatozoa were treated with adriamycin at different concentrations. gammaH2AX was analyzed by immunofluorescent staining and flow cytometry and double-strand breaks (DSB) were detected by the comet assay. RESULTS: The neutral comet assay revealed that the treatment with adriamycin at 2 microg/mL for different times (0.5, 2, 8 and 24 h), or for 8 h at different concentrations (0.4, 2 and 10 microg/mL), induced significant DSB in spermatozoa. Immunofluorent staining and flow cytometry showed that the expression of gH2AX was increased in a dose-dependent and time-dependant manner after the treatment of adriamycin. Adriamycin also induced the concurrent appearance of DNA maintenance/repair proteins RAD50 and 53BP1 with gammaH2AX in spermatozoa. Wortmannin, an inhibitor of the phosphatidylinositol 3-kinase (PI3K) family, abolished the co-appearance of these two proteins with gammaH2AX. CONCLUSION: Human mature spermatozoa have the same response to DSB-induced H2AX phosphorylation and subsequent recruitment of DNA maintenance/repair proteins as somatic cells.
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Thomas M. Marti, Eli Hefner, Luzviminda Feeney et al. · Proceedings of the National Academy of Sciences · 2006 · 355 citations · Full text