Volume 10, Issue 5 (September 2008) 10, 749–757; 10.1111/j.1745-7262.2008.00400.x
Adriamycin induces H2AX phosphorylation in human spermatozoa
Zhong-Xiang Li1,*, Ting-Ting Wang1, Yan-Ting Wu1, Chen-Ming Xu1, Min-Yue Dong1, Jian-Zhong Sheng2 and He-Feng Huang1
1 Department of Reproductive Endocrinology, Women’s Hospital, Zhejiang University School of Medicine, Hangzhou 310006, China 2 Department of Pharmacology and Therapeutics, Faculty of Medicine, University of Calgary, Calgary, Alberta T2N 4N1, Canada
* Current mailing address: Zhejiang Academy of Medical Sciences, Hangzhou 310013, China.
Correspondence: Prof. He-Feng Huang, E-mail: huanghefg@hotmail.com
Received 27 September 2007; Accepted 20 February 2008
Abstract |
Aim: To investigate whether adriamycin induces DNA damage and the formation of γH2AX (the phosphorylated form of histone H2AX) foci in mature spermatozoa.
Methods: Human spermatozoa were treated with adriamycin at different concentrations. γH2AX 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 μg/mL for different times (0.5, 2, 8 and 24 h), or for 8 h at different concentrations (0.4, 2 and 10 μg/mL), induced significant DSB in spermatozoa. Immunofluorent staining and flow cytometry showed that the expression of γH2AX 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 γH2AX in spermatozoa. Wortmannin, an inhibitor of the phosphatidylinositol 3-kinase (PI3K) family, abolished the co-appearance of these two proteins with γH2AX.
Conclusion: Human mature spermatozoa have the same response to DSB-induced H2AX phosphorylation and subsequent recruitment of DNA maintenance/ repair proteins as somatic cells.
Keywords: adriamycin, human spermatozoa, DNA double strand-breaks, γH2AX
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