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Effect of estrogen on the expression of luteinizing hormone-human chorionic gonadotropin receptor messenger ribonucleic acid in cultured rat granulosa cells.

机译:雌激素对培养的大鼠颗粒细胞中促黄体生成素-人绒毛膜促性腺激素受体信使核糖核酸表达的影响。

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Estrogen has been considered to enhance FSH actions in the ovary, including the induction of the LH receptor (LHR). In this study, we elucidated the mechanism underlying the effect of estrogen on the induction of LHR by FSH in rat granulosa cells. Estradiol clearly enhanced the FSH-induced LHR mRNA increase in a time- and dose-dependent manner, with a maximum increase of approximately 3.5-fold at 72 h, compared with the level of LHR mRNA solely induced by FSH. We then investigated whether the effect of estrogen on LHR mRNA was due to increased transcription and/or altered mRNA stability. A luciferase assay with the plasmid containing the LHR 5'-flanking region did not show that estradiol increased the promoter activity induced by FSH. In contrast, the decay curves for LHR mRNA showed a significant increase in half-life with FSH and estradiol, suggesting that the increased stability of LHR mRNA is at least responsible for the regulation of LHR mRNA by estrogen. Recently mevalonate kinase (Mvk) was identified as a trans-factor that binds to LHR mRNA and alters LHR mRNA stability in the ovary. We found that estradiol, with FSH, decreased Mvk mRNA levels in rat granulosa cell culture, resulting in up-regulation of LHR mRNA that was inversely correlated to Mvk mRNA expression. Furthermore, the augmentation of FSH-induced LHR expression in the presence of estrogen was erased with the overexpression of Mvk by transient transfection. Taken together, these data indicate that LHR mRNA is up-regulated due to increased stability when estrogen negatively controls Mvk.
机译:雌激素被认为可以增强卵巢中FSH的作用,包括诱导LH受体(LHR)。在这项研究中,我们阐明了雌激素对FSH诱导大鼠颗粒细胞LHR诱导作用的潜在机制。雌二醇明显地以时间和剂量依赖性方式增强了FSH诱导的LHR mRNA的增加,与仅由FSH诱导的LHR mRNA的水平相比,在72 h时最大增加了约3.5倍。然后,我们调查了雌激素对LHR mRNA的影响是否是由于转录增加和/或mRNA稳定性改变所致。用含有LHR 5'侧翼区的质粒进行的荧光素酶测定未显示雌二醇增加了FSH诱导的启动子活性。相比之下,LHR mRNA的衰减曲线显示FSH和雌二醇的半衰期显着增加,这表明LHR mRNA稳定性的提高至少是雌激素对LHR mRNA调节的原因。最近,甲羟戊酸激酶(Mvk)被鉴定为与LHR mRNA结合并改变LHR mRNA在卵巢中稳定性的反式因子。我们发现雌二醇和FSH降低了大鼠颗粒细胞培养物中Mvk mRNA的水平,导致LHR mRNA的上调与Mvk mRNA的表达呈负相关。此外,通过瞬时转染使Mvk的过表达消除了在雌激素存在下FSH诱导的LHR表达的增强。综上所述,这些数据表明,当雌激素负性控制Mvk时,由于稳定​​性增加,LHR mRNA被上调。

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