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首页> 外文期刊>Reproductive Biology and Endocrinology >Expression of the T regulatory cell transcription factor FoxP3 in peri-implantation phase endometrium in infertile women with endometriosis
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Expression of the T regulatory cell transcription factor FoxP3 in peri-implantation phase endometrium in infertile women with endometriosis

机译:T调节细胞转录因子FoxP3在子宫内膜异位症不孕妇女着床期子宫内膜的表达

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Background Endometriosis (EM) is highly associated with infertility. The precise mechanism underlying EM-associated infertility remains controversial. This study aimed to investigate the pathogenesis of infertility in women with EM by comparing FoxP3+ T regulatory cells (Tregs) expression in the eutopic endometrium of infertile women with EM and endometrium from healthy fertile women. Methods As a marker of Tregs , FoxP3 expression was analyzed in eutopic endometrium during the peri-implantation phase in infertile women with mild EM (n?=?7), advanced EM (n?=?20), and normally fertile women without EM (n?=?20). FoxP3 mRNA expression was analyzed by quantitative real-time RT-PCR. FoxP3 protein expression was assessed by immunohistochemistry. Results FoxP3 mRNA expression in all infertile patients with EM was significantly higher than the control group (P?U-test. Further analysis based on the extent of EM revealed that FoxP3 mRNA expression in infertile patients with advanced EM was significantly higher than the mild EM group and the control group (P?P?>?0.05) by two-tailed t-tests. Conclusions These findings suggest that FoxP3+ Tregs in the peri-implantation endometrium might participate in the pathogenesis of advanced EM. However, they are not directly involved in the pathogenesis of advanced EM associated with infertility. The differential expression of FoxP3 in infertile women with mild EM and advanced EM implicates that notable differences in the uterine immune status are likely involved in the pathogenesis of mild EM associated with infertility in the peri-implantation endometrium.
机译:背景子宫内膜异位症(EM)与不孕症高度相关。 EM相关性不孕症的确切机制仍存在争议。这项研究旨在通过比较不育妇女和健康受孕妇女子宫内膜的异位内膜中FoxP3 + T调节细胞(Tregs)的表达来调查EM妇女不育的发病机理。方法分析轻度EM(n?=?7),晚期EM(n?=?20)和不具有EM的正常可育女性在围着床期的异位子宫内膜中Fox的表达,作为Tregs的标志物。 (n?=?20)。通过定量实时RT-PCR分析FoxP3 mRNA表达。通过免疫组织化学评估FoxP3蛋白表达。结果所有不育症EM患者的FoxP3 mRNA表达均显着高于对照组(P?U检验)。根据EM的程度进一步分析发现,晚期EM不育患者FoxP3 mRNA表达显着高于轻度EM结论:这些结果提示植入后子宫内膜的FoxP3 + Tregs可能参与了晚期EM的发病机制,但两组均无统计学意义(P> P?>?0.05)。 FoxP3在患有轻度EM和晚期EM的不育妇女中的差异表达表明,子宫免疫状态的显着差异可能参与了轻度EM与围产期不育相关的发病机理。植入子宫内膜。

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