Méndez Eva, Montserrat Núria, Planas Josep V
Departament de Fisiologia, Facultat de Biologia, Universitat de Barcelona, Av. Diagonal 645, 08028 Barcelona, Spain.
Mol Cell Endocrinol. 2005 Jan 14;229(1-2):49-56. doi: 10.1016/j.mce.2004.09.006.
In the salmonid ovary, luteinizing hormone (LH) is the major gonadotropic hormone stimulating the production of steroids during the periovulatory period and its effects are mediated by the cAMP-dependent protein kinase (PKA) signaling pathway. We have previously shown that the in vitro steroidogenic activity of LH in the salmonid ovary is inhibited by insulin-like growth factor I (IGF-I) which, like insulin, has specific receptors in both theca and granulosa layers. In the present study, we have investigated the modulatory effects of insulin on salmon LH (sLH)-stimulated steroid production in preovulatory theca layers of brown trout (Salmo trutta) and the effects of both insulin and IGF-I on the sLH-stimulated cAMP/PKA signaling pathway. Our results show that insulin, like IGF-I, blocked the stimulatory effects of sLH, dibutyryl cAMP and IBMX on testosterone (T) production but not those of sLH on cAMP production. Furthermore, insulin and IGF-I blocked the activation of PKA induced by sLH and these effects were correlated with changes in the total protein content of the catalytic (C) and type II regulatory (RII) subunits of PKA. Interestingly, insulin and IGF-I had different effects on total PKA subunit content since insulin potentiated the sLH-stimulated increase in RII subunit content whereas IGF-I blocked the sLH-stimulated increase in total C subunit content. The effects of insulin and IGF-I in trout theca layers appeared to be mediated by the mitogen-activated protein kinase (MAPK) signaling pathway because inhibition of extracellular signal-regulated kinase 1/2(ERK1/2) activity completely blocked the inhibitory effects of insulin and IGF-I on the sLH-stimulated production of T and because insulin and IGF-I increased the total protein content of ERK1/2 in trout theca layers. Therefore, our results suggest that insulin and IGF-I, probably through the MAPK pathway, block the action of sLH in trout theca layers by modulating the cAMP/PKA signaling pathway.
在鲑科鱼类卵巢中,促黄体生成素(LH)是在排卵前期刺激类固醇生成的主要促性腺激素,其作用由环磷酸腺苷(cAMP)依赖性蛋白激酶(PKA)信号通路介导。我们之前已经表明,鲑科鱼类卵巢中LH的体外类固醇生成活性受到胰岛素样生长因子I(IGF-I)的抑制,IGF-I与胰岛素一样,在卵泡膜层和颗粒层均具有特异性受体。在本研究中,我们研究了胰岛素对褐鳟(Salmo trutta)排卵前卵泡膜层中鲑鱼促黄体生成素(sLH)刺激的类固醇生成的调节作用,以及胰岛素和IGF-I对sLH刺激的cAMP/PKA信号通路的影响。我们的结果表明,胰岛素与IGF-I一样,阻断了sLH、二丁酰cAMP和异丁基甲基黄嘌呤(IBMX)对睾酮(T)生成的刺激作用,但未阻断sLH对cAMP生成的刺激作用。此外,胰岛素和IGF-I阻断了sLH诱导的PKA激活,这些作用与PKA催化(C)亚基和II型调节(RII)亚基的总蛋白含量变化相关。有趣的是,胰岛素和IGF-I对PKA总亚基含量有不同影响,因为胰岛素增强了sLH刺激的RII亚基含量增加,而IGF-I阻断了sLH刺激的总C亚基含量增加。胰岛素和IGF-I在鳟鱼卵泡膜层中的作用似乎由丝裂原活化蛋白激酶(MAPK)信号通路介导,因为抑制细胞外信号调节激酶1/2(ERK1/2)活性完全阻断了胰岛素和IGF-I对sLH刺激的T生成的抑制作用,并且胰岛素和IGF-I增加了鳟鱼卵泡膜层中ERK1/2的总蛋白含量。因此,我们的结果表明,胰岛素和IGF-I可能通过MAPK通路,通过调节cAMP/PKA信号通路来阻断sLH在鳟鱼卵泡膜层中的作用。