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Effect of gold nanoparticles on mouse spermatogenesis
Authors:S T Zakhidov  S M Pavlyuchenkova  T L Marshak  V M Rudoy  O V Dement’eva  I A Zelenina  S G Skuridin  A A Makarov  A N Khokhlov  Yu M Evdokimov
Institution:1. Biological Faculty, Moscow State University, Leninskie gory 1, Moscow, 119991, Russia
2. Koltzov Institute of Developmental Biology, ul. Vavilova 26, Moscow, 119334, Russia
3. Frumkin Institute of Physical Chemistry and Electrochemistry, Leninskii prospect 31, Moscow, 119071, Russia
4. Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, ul. Vavilova 32, Moscow, 119334, Russia
5. National Research University Higher School of Economics, ul. Myasnitskaya 20, Moscow, 101000, Russia
Abstract:The response of the mouse male germ cells exposed to gold nanoparticles (??2.5 nm) was studied. Our investigation demonstrates that treatment with Au nanoparticles for four days does not impair the architecture of the spermatogenic epithelium. Cytogenetic evaluation using micronucleus assay showed that gold nanoparticles can affect the chromosomes of early primary spermatocytes. However, gold nanoparticles did not induce chromosome abnormalities in spermatogonial stem cells. Further, the cauda epididymal sperm was isolated on the 14th day after treatment and was incubated in SDS solution (Na dodecyl sulphate) and then in a solution containing DTT (dithiothreitol) to induce nuclear chromatin decondensation. Observations showed that after four days of treatment of spermiogenic (postmeiotic) cells with gold nanoparticles the decondensation process had no differences from the control. On the contrary, in the experiment with the same cells and period of fixation but with a single exposure to gold nanoparticles, the number of mature gametes with totally decondensed nuclei reached 100% as opposed to 44% in the controls.
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