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Expressions of transcription factors Ets1 and Ets2 in mouse testis tissue

机译:小鼠睾丸组织中转录因子Ets1和Ets2的表达

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To investigate the regulation of Ets family transcription factors Ets1 and Ets2 on the development of mouse testis and elucidate the effects of Ets1 and Ets2 on self-renewal and differentiation of spermatogonial stem cells. Mouse testis tissues were collected from specific developmental stages including the postnatal days 1, 5, 10, 15, 20, 25, 30, 35, 40, 50 and 70; busulfan peritoneal injection was performed and mouse testis tissues were collected on the 0th, 3rd, 5th, 8th, 10th, 18th days after injection respectively. The mRNA expression levels of Ets1 and Ets2 in samples were analyzed by semi-quantitative RT-PCR. The expression of Ets1 was significantly higher during the period of postnatal 1∼30 day than that at postnatal day 35 (P<0.05 or 0.01), while its expression decreased evidently and maintained at a stable level afterwards. Ets2 expressed significantly higher during the period of postnatal 1∼25 day than that at postnatal day 35 (P<0.05 or 0.01), while it decreased significantly and maintained at a stable level afterwards similarly. After busulfan treatment, the expression of Ets1 declined and reached the lowest level at day 5, then increased gradually and reached the level of day 0 after busulfan treatment and maintained steadily around day 9. Notably, the expressions of Ets1 at day 5 and day 8 were significantly higher than that of day 0 after busulfan treatment (P<0.05 or 0.01). No obvious changes was observed for the expression of Ets2 during 1∼9 day after busulfan treatment, while it decreased dramatically at day 10, which was significantly lower than that of day 0 and day 18 (P<0.05 or 0.01). The expression of Ets2 gradually increased after day 10 and reached its normal level around day 18. Taken together, Ets1 and Ets2 may affect the early development of mouse testis, adult spermatogenesis, as well as the proliferation and differentiation of spermatogonia.
机译:研究Ets家族转录因子Ets1和Ets2对小鼠睾丸发育的调控,并阐明Ets1和Ets2对精原干细胞自我更新和分化的影响。从特定的发育阶段收集小鼠睾丸组织,包括出生后的第1、5、10、15、20、25、30、35、40、50和70天;于注射后第0、3、5、8、10、18天分别进行白消安腹膜注射,并收集小鼠睾丸组织。通过半定量RT-PCR分析样品中Ets1和Ets2的mRNA表达水平。出生后1〜30天,Ets1的表达明显高于出生后第35天(P <0.05或0.01),而Ets1的表达明显下降,此后保持稳定。出生后1〜25天,Ets2的表达明显高于出生后第35天(P <0.05或0.01),而Ets2则显着下降并随后保持稳定。白消安处理后,Ets1的表达下降,并在第5天达到最低水平,然后逐渐增加并达到白消安处理后的第0天的水平,并稳定在第9天左右。值得注意的是,Ets1的表达在第5天和第8天保持稳定。白消安治疗后第0天显着高于对照组(P <0.05或0.01)。白消安治疗后1〜9天,Ets2的表达未见明显变化,而在第10天Ets2的表达急剧下降,明显低于第0天和第18天(P <0.05或0.01)。 Ets2的表达在第10天后逐渐增加,并在第18天左右达到正常水平。Ets1和Ets2在一起可能会影响小鼠睾丸的早期发育,成年精子的生成以及精原细胞的增殖和分化。

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