Weiss Jürgen M, Hüller Heike, Polack Stephan, Friedrich Michael, Diedrich Klaus, Treeck Oliver, Pfeiler Georg, Ortmann Olaf
Department of Obstetrics and Gynaecology, University of Luebeck, Luebeck, Germany.
J Mol Endocrinol. 2007 Feb;38(1-2):305-14. doi: 10.1677/jme.1.02114.
Long-term treatment with estradiol increases LH secretion from female gonadotrophs. The mechanisms are not fully clarified yet. Our previous data indicated that sexual steroids might affect late steps in GnRH signal transduction such as exocytosis. The secretion of hormones from neuroendocrine cells requires the merger of secretory vesicles with the plasma membrane. This regulated exocytosis is mediated by specific proteins, which are present in the pituitary gland. Here, we examined whether two of these crucial exocytotic proteins, SNAP-25 and munc-18, are affected by estradiol in female gonadotrophs. Female rat anterior pituitary cells and alphaT3-1 cells, derived from a murine immortalized gonadotroph cell line, were treated with 100 pM estradiol for 48 h. LH secretion of anterior pituitary cells, additionally stimulated with eight consecutive pulses of 1 nM GnRH for 15 min at an interval of 1 h, was determined by RIA. Gene expression was measured by quantitative RT-PCR and protein expression by immunoblotting. Additionally, quantitative RT-PCR was performed in single rat gonadotrophs to ascribe effects exclusively to intact gonadotrophs. Pulsatile GnRH enhanced the mRNA expression of SNAP-25 and munc-18 in accordance with the LH secretory response with the greatest increase at the third pulse of GnRH. Estradiol treatment further increased GnRH-induced LH secretion at all GnRH pulses. SNAP-25 gene expression was significantly decreased at the fifth GnRH pulse and unaffected at basal after 48 h of estradiol treatment. In contrast, munc-18 mRNA levels were not significantly affected by estradiol at different GnRH-pulses in mixed anterior pituitary cells, whereas munc-18 gene expression was significantly increased at basal. In alphaT3-1 cells and single gonadotrophs, long-term estradiol treatment significantly reduced SNAP-25 protein and gene expression. In contrast, the protein and gene expression of munc-18 was significantly enhanced in both alphaT3-1 cells and single gonadotrophs. In conclusion, munc-18 and SNAP-25 were oppositionally influenced by estradiol. The results suggest that estradiol modulates the expression of exocytotic proteins in gonadotrophs and thus affects LH secretion.
雌二醇长期治疗可增加雌性促性腺激素细胞的促黄体生成素(LH)分泌。其机制尚未完全阐明。我们之前的数据表明,性类固醇可能会影响GnRH信号转导的后期步骤,如胞吐作用。神经内分泌细胞分泌激素需要分泌小泡与质膜融合。这种受调控的胞吐作用由垂体中存在的特定蛋白质介导。在此,我们研究了这两种关键的胞吐蛋白,即SNAP - 25和munc - 18,是否受雌二醇影响雌性促性腺激素细胞。将源自小鼠永生化促性腺激素细胞系的雌性大鼠垂体前叶细胞和αT3 - 1细胞用100 pM雌二醇处理48小时。通过放射免疫分析(RIA)测定垂体前叶细胞在另外以1小时间隔连续8次给予1 nM GnRH脉冲刺激15分钟后的LH分泌。通过定量逆转录聚合酶链反应(RT - PCR)测量基因表达,通过免疫印迹测量蛋白质表达。此外,在单个大鼠促性腺激素细胞中进行定量RT - PCR,以仅将效应归因于完整的促性腺激素细胞。脉冲式GnRH增强了SNAP - 25和munc - 18的mRNA表达,与LH分泌反应一致,在GnRH的第三个脉冲时增加最大。雌二醇处理在所有GnRH脉冲时进一步增加了GnRH诱导的LH分泌。在雌二醇处理48小时后,SNAP - 25基因表达在第五个GnRH脉冲时显著降低,在基础状态下未受影响。相比之下,在混合的垂体前叶细胞中,不同GnRH脉冲时munc - 18的mRNA水平未受雌二醇显著影响,而基础状态下munc - 18基因表达显著增加。在αT3 - 1细胞和单个促性腺激素细胞中,长期雌二醇处理显著降低了SNAP - 25蛋白和基因表达。相比之下,αT3 - 1细胞和单个促性腺激素细胞中munc - 18的蛋白和基因表达均显著增强。总之,munc - 18和SNAP - 25受雌二醇的相反影响。结果表明,雌二醇调节促性腺激素细胞中胞吐蛋白的表达,从而影响LH分泌。