MD, Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale University School of Medicine, 310 Cedar Street, LSOG 304B, New Haven, Connecticut 06520-8063.
Endocrinology. 2013 Oct;154(10):3877-87. doi: 10.1210/en.2013-1341. Epub 2013 Aug 2.
GnRH agonists (GnRHa) are increasingly used for fertility preservation in women undergoing gonadotoxic chemotherapy. However, the protective mechanisms of action for these compounds have not yet been elucidated. In this study, we aimed to determine whether GnRHa have a direct effect on ovarian granulosa cells. GnRH receptor (GnRHR) expression was determined in mouse somatic and gonadal tissues including granulosa/cumulus cells and oocytes using quantitative RT-PCR and immunohistochemistry. Granulosa cells were isolated from mouse ovaries primed with pregnant mare serum gonadotropin. Response to GnRHa in cultured granulosa cells was assessed by determining the increase of intracellular cAMP and by assessing phosphorylation of downstream mediators of GnRH signaling: ERK and p38. To measure intracellular cAMP in our system, the cells were transfected with a cAMP-responsive luciferase reporter plasmid and stimulated with GnRHa. For all experiments, pituitary tissue and/or the αT3-1 mouse pituitary cell line were used as controls. GnRHR mRNA and protein were detected in mouse ovaries, granulosa/cumulus cells, and oocytes. After GnRHa stimulation at various time intervals, we were unable to detect a cAMP increase or activation of the ERK or p38 signaling pathway in cultured primary mouse granulosa cells, whereas activation was detected in the control αT3-1 mouse pituitary cells. In this study, we have not detected activation of the canonical GnRH signaling pathways in mouse ovarian somatic cells. Our findings suggest that the mechanism of action of GnRHa in the ovary is either below the detection level of our experimental design or is different from that in the pituitary.
促性腺激素释放激素激动剂(GnRHa)越来越多地用于接受性腺毒性化疗的女性的生育力保存。然而,这些化合物的作用保护机制尚未阐明。在这项研究中,我们旨在确定 GnRHa 是否对卵巢颗粒细胞有直接作用。使用定量 RT-PCR 和免疫组织化学法测定了包括颗粒细胞/卵丘细胞和卵母细胞在内的小鼠体组织和性腺组织中的促性腺激素释放激素受体(GnRHR)表达。用孕马血清促性腺激素预刺激小鼠卵巢以分离颗粒细胞。通过测定细胞内 cAMP 的增加以及评估 GnRH 信号转导的下游介质 ERK 和 p38 的磷酸化来评估培养的颗粒细胞对 GnRHa 的反应。为了在我们的系统中测量细胞内 cAMP,将细胞用 cAMP 反应性荧光素酶报告质粒转染并用 GnRHa 刺激。对于所有实验,均使用垂体组织和/或αT3-1 小鼠垂体细胞系作为对照。在小鼠卵巢、颗粒细胞/卵丘细胞和卵母细胞中检测到 GnRHR mRNA 和蛋白。在 GnRHa 刺激不同时间间隔后,我们未能检测到培养的原代小鼠颗粒细胞中 cAMP 的增加或 ERK 或 p38 信号通路的激活,而在对照的αT3-1 小鼠垂体细胞中检测到了激活。在这项研究中,我们未检测到小鼠卵巢体细胞中经典 GnRH 信号通路的激活。我们的研究结果表明,GnRHa 在卵巢中的作用机制要么低于我们的实验设计的检测水平,要么与垂体中的作用机制不同。