Morera A M, Esposito G, Ghiglieri C, Chauvin M A, Hartmann D J, Benahmed M
INSERM CJF 90-08, Laboratoire de Biochimie, Hôpital Sainte Eugénie, Pierre-Bénite, France.
Endocrinology. 1992 Feb;130(2):831-6. doi: 10.1210/endo.130.2.1370796.
In the present study, we have tested the effects of transforming growth factor beta 1 (TGF beta 1) on FSH action toward aromatase activity and lactate production in cultured Sertoli cells isolated from immature porcine testes. Whereas treatment of Sertoli cells with FSH resulted in a dose-dependent increase (about 7-fold) in aromatase activity (conversion of testosterone into estradiol) (ED50 = 80 ng/ml FSH), the addition of TGF beta 1 reduced this gonadotropin action. The inhibitory effect of TGF beta 1 on FSH aromatase activity was dose dependent (ED50 = 0.1 ng/ml, 4 pM TGF beta 1) with a maximal decrease (about 40%) observed after a long term (48-h) treatment. TGF beta 1 exerted its inhibitory effect on FSH action at the level(s) of cAMP accumulation, exerting no apparent effect on the gonadotropin receptor or at a site(s) related to cAMP action. TGF beta 1 (2 ng/ml) significantly (P less than 0.002) reduced (52% decrease) FSH-stimulated cAMP levels in cultured porcine Sertoli cells. However, such an inhibitory effect of the growth factor was no longer observed when stimulation of cAMP accumulation with FSH occurred in the presence of methyl isobutyl xanthine (0.5 mM), an inhibitor of cAMP-phosphodiesterase activity. This observation suggests that TGF beta 1 decreased cAMP levels by increasing catabolism of the cyclic nucleotide through an enhancement of cAMP-phosphodiesterase activity. The inhibitory effect of TGF beta 1 was not limited to the action of FSH on aromatase activity but also extended to the gonadotropin action (mediated by cAMP) on lactate production. As for the inhibitory effect of TGF beta 1 on FSH-induced aromatase activity, the inhibitory effect of the growth factor on FSH-stimulated lactate production was dose and time dependent with a maximal decrease (about 30%) observed in the picomolar range (1 ng/ml, 40 pM) after 48 h treatment with TGF beta 1. In conclusion, the present study demonstrates that TGF beta 1 attenuates FSH action on Sertoli cell activity and that such inhibitory action is potentially exerted through a decrease in cAMP levels. Because of the local production of TGF beta 1, it is suggested that the effects of the growth factor reported here might be exerted in the context of the testicular paracrine mechanisms.
在本研究中,我们检测了转化生长因子β1(TGFβ1)对促卵泡激素(FSH)作用于从未成熟猪睾丸分离的培养支持细胞中芳香化酶活性和乳酸生成的影响。用FSH处理支持细胞会导致芳香化酶活性(睾酮转化为雌二醇)呈剂量依赖性增加(约7倍)(ED50 = 80 ng/ml FSH),而添加TGFβ1会降低这种促性腺激素的作用。TGFβ1对FSH芳香化酶活性的抑制作用呈剂量依赖性(ED50 = 0.1 ng/ml,4 pM TGFβ1),长期(48小时)处理后观察到最大降幅(约40%)。TGFβ1在cAMP积累水平上对FSH作用发挥抑制作用,对促性腺激素受体或与cAMP作用相关的位点无明显影响。TGFβ1(2 ng/ml)显著(P < 0.002)降低(降低52%)培养的猪支持细胞中FSH刺激的cAMP水平。然而,当在存在甲基异丁基黄嘌呤(0.5 mM)(一种cAMP磷酸二酯酶活性抑制剂)的情况下用FSH刺激cAMP积累时,不再观察到这种生长因子的抑制作用。这一观察结果表明,TGFβ1通过增强cAMP磷酸二酯酶活性增加环核苷酸的分解代谢从而降低cAMP水平。TGFβ1的抑制作用不仅限于FSH对芳香化酶活性的作用,还扩展到促性腺激素(由cAMP介导)对乳酸生成的作用。至于TGFβ1对FSH诱导的芳香化酶活性的抑制作用,生长因子对FSH刺激的乳酸生成的抑制作用呈剂量和时间依赖性,在用TGFβ1处理48小时后,在皮摩尔范围内(1 ng/ml,40 pM)观察到最大降幅(约30%)。总之,本研究表明TGFβ1减弱FSH对支持细胞活性的作用,且这种抑制作用可能是通过降低cAMP水平来实现的。由于TGFβ1是局部产生的,因此提示本文报道的生长因子的作用可能是在睾丸旁分泌机制的背景下发挥的。