Ajdary Marziyeh, Zandieh Zahra, Amjadi Fatemeh Sadat, Keyhanfar Fariborz, Mehdizadeh Mehdi, Aflatoonian Reza
Endometriosis Research Center, Iran University of Medical Sciences, Tehran, Iran.
Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Int J Reprod Biomed. 2020 Oct 13;18(10):815-824. doi: 10.18502/ijrm.v13i10.7765. eCollection 2020 Oct.
Many researchers consider implantation and endometrial receptivity as pertinent issues in reproductive science. Although, several experiments have been performed and their results evaluated, yet there is no confirmed evidence about the related factors and the role of sperm in endometrial receptivity.
To investigate the effect of the sperm-endometrium interaction in regulating genes involved in the endometrial receptivity pathway.
In this experimental study, 10 male and 30 female NMRI mice were included, and half of the male cases were vasectomized. The subjects were divided into two groups as follows; group 1 (case) comprised of 15 females mated with 5 non-vasectomized male mice, while group 2 (control) consisted of 15 females mated with 5 vasectomized males. Cases were sacrificed and assessed after 36 hr and the endometrial tissue was extracted and kept at -80°C until the next use. The expression of the endometrial receptivity pathway genes, including and was examined in both groups. For statistical analysis, an independent samples test (Mean SD) was used.
The mRNA levels of (p = 0.045), (p = 0.040), (p = 0.032), (p = 0.022), (p = 0.035), (p = 0.040) were significantly upregulated in the case group compared with the control group.
Finally, seminal plasma was observed to be effective in expressing the involved genes in the successful implantation pathway, including and .
许多研究人员认为着床和子宫内膜容受性是生殖科学中的相关问题。尽管已经进行了多项实验并对结果进行了评估,但关于相关因素以及精子在子宫内膜容受性中的作用仍没有确凿证据。
研究精子与子宫内膜相互作用对调节子宫内膜容受性途径相关基因的影响。
在这项实验研究中,纳入了10只雄性和30只雌性NMRI小鼠,其中一半雄性小鼠进行了输精管切除术。将实验对象分为两组,如下:第1组(病例组)由15只与5只未进行输精管切除术的雄性小鼠交配的雌性小鼠组成,而第2组(对照组)由15只与5只进行了输精管切除术的雄性小鼠交配的雌性小鼠组成。36小时后处死病例组小鼠并进行评估,提取子宫内膜组织并保存在-80°C直至下次使用。检测两组中子宫内膜容受性途径基因的表达,包括 和 。进行统计分析时,使用独立样本检验(均值±标准差)。
与对照组相比,病例组中 (p = 0.045)、 (p = 0.040)、 (p = 0.032)、 (p = 0.022)、 (p = 0.035)、 (p = 0.040)的mRNA水平显著上调。
最后,观察到精浆在成功着床途径中对包括 和 在内的相关基因表达具有影响。