Imai T, Kurachi H, Adachi K, Adachi H, Yoshimoto Y, Homma H, Tadokoro C, Takeda S, Yamaguchi M, Sakata M
Department of Obstetrics and Gynecology, Osaka University Medical School, Japan.
Biol Reprod. 1995 Apr;52(4):928-38. doi: 10.1095/biolreprod52.4.928.
We examined menstrual cycle-dependent changes in the expression of human endometrial epidermal growth factor (EGF), transforming growth factor alpha (TGF alpha), and epidermal growth factor receptor (EGFR) and their mRNA using immunoblot analysis, 125I-EGF binding, and competitive reverse transcription and polymerase chain reaction (RT-PCR). We also studied their localization in the endometrial tissue by immunohistochemistry. Endometrial samples were obtained at three stages of menstruation: the early follicular stage, which exhibits low serum estradiol (E2) and progesterone (P) levels; the late follicular stage, which exhibits high E2 and low P levels; and the luteal stage, which exhibits high E2 and P levels. Immunohistochemical examination showed that EGF, TGF alpha, and EGFR were localized to the endometrial epithelium. Immunoblot analysis revealed that endometrial EGF, TGF alpha, and EGFR levels were significantly (p < 0.01) increased at the late follicular and luteal stages compared to the early follicular stage. 125I-EGF-specific binding levels at the late follicular and luteal stages were significantly (p < 0.01) higher than at the early follicular stage, consistent with the results of immunoblot analysis. Competitive RT-PCR revealed that EGF, TGF alpha, and EGFR mRNA levels were significantly (p < 0.01) higher at the late follicular and luteal stages than at the early follicular stage. Changes in EGF, TGF alpha, and EGFR mRNA levels were consistent with changes in protein levels. These findings suggest that synthesis and expression of human endometrial EGF, TGF alpha, and EGFR vary with the stage of the menstrual cycle and that their expression in the human endometrium is associated with the increase in the serum E2 but not with the increase in P levels.
我们使用免疫印迹分析、¹²⁵I-表皮生长因子(EGF)结合以及竞争性逆转录聚合酶链反应(RT-PCR),研究了人子宫内膜表皮生长因子(EGF)、转化生长因子α(TGFα)和表皮生长因子受体(EGFR)及其mRNA表达的月经周期依赖性变化。我们还通过免疫组织化学研究了它们在子宫内膜组织中的定位。在月经的三个阶段获取子宫内膜样本:卵泡早期,此时血清雌二醇(E2)和孕酮(P)水平较低;卵泡晚期,此时E2水平高而P水平低;黄体期,此时E2和P水平均高。免疫组织化学检查显示,EGF、TGFα和EGFR定位于子宫内膜上皮。免疫印迹分析显示,与卵泡早期相比,卵泡晚期和黄体期子宫内膜EGF、TGFα和EGFR水平显著升高(p < 0.01)。卵泡晚期和黄体期¹²⁵I-EGF特异性结合水平显著高于卵泡早期(p < 0.01),与免疫印迹分析结果一致。竞争性RT-PCR显示,卵泡晚期和黄体期EGF、TGFα和EGFR mRNA水平显著高于卵泡早期(p < 0.01)。EGF、TGFα和EGFR mRNA水平的变化与蛋白质水平的变化一致。这些发现表明,人子宫内膜EGF、TGFα和EGFR的合成和表达随月经周期阶段而变化,并且它们在人子宫内膜中的表达与血清E2升高有关,而与P水平升高无关。