Saragüeta P E, Lanuza G M, Barañao J L
Instituto de Biologia y Medicina Experimental-CONICET, Buenos Aires, Argentina.
Mol Reprod Dev. 1997 Jun;47(2):170-4. doi: 10.1002/(SICI)1098-2795(199706)47:2<170::AID-MRD7>3.0.CO;2-J.
Gonadotropin-releasing hormone (GnRH) has been found to be expressed within the ovary and to modulate cell differentiation in ovarian cells. In the present study we have analyzed the influence of GnRH on DNA synthesis in rat granulosa cells. Cells were obtained from immature DES-treated rats and cultured in defined medium (DMEM:F12) containing combinations of FSH, estradiol, and transforming growth factor-beta (TGF-beta), both in the presence and absence of GnRH. A GnRH analog, Leuprolide (GnRHa), caused a dose-dependent inhibition of 3H-thymidine incorporation in cells cultured in the presence of FSH (20 ng/ml) and TGF beta (2.5 ng/ml), at concentrations as low as 5 x 10(-11) M. Similarly, a complete inhibition of hormonally stimulated DNA synthesis were observed with another analog (Buserelin, ED50 = 1.58 +/- 0.22 x 10(-10) M) and native GnRH (ED50 = 1.4 +/- 0.3 x 10(-6) M). A competitive antagonist of GnRH (Antide) was used to neutralize the GnRH agonist effects. Antide 10(-8) M could prevent the inhibition elicited by 10(-7) M of Leuprolide. These results suggest that GnRH may play a role in the regulation of rat granulosa cell proliferation during follicular development.
促性腺激素释放激素(GnRH)已被发现在卵巢内表达,并调节卵巢细胞的分化。在本研究中,我们分析了GnRH对大鼠颗粒细胞DNA合成的影响。细胞取自未成熟的己烯雌酚处理大鼠,并在含有促卵泡激素(FSH)、雌二醇和转化生长因子-β(TGF-β)组合的限定培养基(DMEM:F12)中培养,培养时分别添加和不添加GnRH。一种GnRH类似物,亮丙瑞林(GnRHa),在低至5×10⁻¹¹ M的浓度下,就能对在FSH(20 ng/ml)和TGF-β(2.5 ng/ml)存在下培养的细胞中的³H-胸腺嘧啶核苷掺入产生剂量依赖性抑制。同样,另一种类似物(布舍瑞林,ED50 = 1.58±0.22×10⁻¹⁰ M)和天然GnRH(ED50 = 1.4±0.3×10⁻⁶ M)也观察到对激素刺激的DNA合成有完全抑制作用。一种GnRH竞争性拮抗剂(Antide)被用于中和GnRH激动剂的作用。10⁻⁸ M的Antide能够阻止10⁻⁷ M亮丙瑞林引起的抑制作用。这些结果表明,GnRH可能在卵泡发育过程中大鼠颗粒细胞增殖的调节中发挥作用。