Unidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología-Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México 11000, Mexico.
Departamento de Genética y Genómica Humana, Instituto Nacional de Perinatología, Mexico.
Biomed Res Int. 2020 Jul 13;2020:2196024. doi: 10.1155/2020/2196024. eCollection 2020.
Endometriosis is one of the most frequent gynecological diseases in reproductive age women, but its etiology is not completely understood. Endometriosis is characterized by progesterone resistance, which has been explained in part by a decrease in the expression of the intracellular progesterone receptor in the ectopic endometrium. Progesterone action is also mediated by nongenomic mechanisms via membrane progesterone receptors (mPRs) that belong to the class II members of the progesterone and adipoQ receptor (PAQR) family. The aim of the present study was to evaluate the expression at mRNA and protein levels of mPR members in the eutopic and ectopic endometrium of women with endometriosis. Total RNA and total protein were isolated from control endometrium (17 samples), eutopic endometrium (17 samples), and ectopic endometrium (9 samples). The expression of (mPR), (mPR), and (mPR) at mRNA and protein levels was evaluated by RT-qPCR and Western blot, whereas (mPR) gene expression was evaluated by RT-qPCR. Statistical analysis between comparable groups was performed using one-way ANOVA followed by Tukey's multiple comparisons test with a confidence interval of 95 %. The analysis of gene expression showed that and expression was lower in both eutopic and ectopic endometrium as compared to the endometrium of women without endometriosis, whereas the expression of and was only reduced in eutopic endometrium. Furthermore, mPR and mPR protein content was decreased in the ectopic endometrium of women with endometriosis. Our results demonstrate a decrease in the expression and protein content of mPRs in eutopic and ectopic endometrium of patients with endometriosis, which could contribute to the progesterone resistance observed in patients with this disease.
子宫内膜异位症是生育期妇女最常见的妇科疾病之一,但病因尚不完全清楚。子宫内膜异位症的特点是孕激素抵抗,部分原因是异位子宫内膜中细胞内孕激素受体的表达减少。孕激素的作用也通过膜孕激素受体(mPRs)介导非基因组机制,膜孕激素受体属于孕激素和脂联素受体(PAQR)家族的 II 类成员。本研究旨在评估子宫内膜异位症患者在位和异位子宫内膜中 mPR 成员的 mRNA 和蛋白水平表达。从对照组子宫内膜(17 例)、在位子宫内膜(17 例)和异位子宫内膜(9 例)中分离总 RNA 和总蛋白。通过 RT-qPCR 和 Western blot 评估 mPR (mPR)、 (mPR)和 (mPR)的 mRNA 和蛋白水平表达,通过 RT-qPCR 评估 (mPR)基因表达。使用单因素方差分析,随后进行 Tukey 多重比较检验,置信区间为 95%,对可比组之间的统计分析。基因表达分析表明,与无子宫内膜异位症的妇女相比,在位和异位子宫内膜中的 和 表达均降低,而 和 的表达仅在在位子宫内膜中降低。此外,子宫内膜异位症患者的异位子宫内膜中 mPR 和 mPR 蛋白含量降低。我们的研究结果表明,子宫内膜异位症患者的在位和异位子宫内膜中 mPRs 的表达和蛋白含量降低,这可能导致该疾病患者孕激素抵抗。