Multimodal control of pituitary gonadotropin biosynthesis. Effects of gonadal steroids, GnRH, cyclic AMP and diacylglycerols.

R Counis, A Starzec, M Corbani, M Jutisz
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引用次数: 3

Abstract

We and others have previously shown that in the rat and the sheep gonadectomy increases the translational capacity of mRNAs encoding gonadotropin subunits alpha, LH beta and FSH beta. Injection of estradiol or of testosterone or dihydrotestosterone depresses the translational capacity of the mRNAs. After using estradiol to induce progesterone receptors in the pituitary of castrated animals, it was determined that progesterone does enhance the inhibitory effect of estradiol. We have also observed this inhibitory effect of gonadal steroids in vitro, suggesting that at least part of the steroid action is exerted at the pituitary level. Hybridization assay (Northern blot) using oligodeoxynucleotide probes complementary to a short portion in the cDNA strand of each subunit, showed gonadal steroids to act by decreasing the number of copies of mRNAs encoding LH and FSH subunits. Using anterior pituitary cells in culture, incubated in the presence of labeled methionine, we have confirmed our previous observation that GnRH stimulates the biosynthesis of the polypeptide chains of LH. This effect is not secondary due to LH release. It is not inhibited when incubation is performed in the presence of tunicamycin, an inhibitor of glycosylation. SDS-polyacrylamide gel electrophoresis of specific immunoprecipitates of polypeptides immunologically related to alpha allowed us to identify 3 forms of alpha-polypeptide differing in their apparent Mr:21K (partially glycosylated), 23K (authentic) and 25K (hyperglycosylated). Besides its stimulatory effect on the release and synthesis of LH, GnRH also stimulated the release of the 23K and 25K forms of alpha. In the presence of tunicamycin an additional 16K form of apoprotein-alpha was detected which accumulated within the cells. A cAMP analogue (8-Br-cAMP), intracellular cAMP generators (choleragen, forskolin), as well as an analogue of diacylglycerols (TPA) mimic the stimulatory action of GnRH. However, although no evidence has been obtained at present that either cAMP or diacylglycerols mediate the GnRH effect on the biosynthesis of the polypeptide chains of LH, our data suggest that phosphorylation of intracellular phosphoproteins plays a major role in this process.

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垂体促性腺激素生物合成的多模式控制。性腺激素,GnRH,环AMP和二酰基甘油的作用。
我们和其他人之前已经证明,在大鼠和羊的性腺切除中,编码促性腺素亚基α、LH β和FSH β的mrna的翻译能力增加。注射雌二醇、睾酮或双氢睾酮可抑制mrna的翻译能力。用雌二醇诱导去势动物垂体内孕酮受体后,确定了黄体酮确实增强了雌二醇的抑制作用。我们还在体外观察到性腺类固醇的这种抑制作用,表明至少部分类固醇作用在垂体水平发挥作用。利用与每个亚基cDNA短链互补的寡脱氧核苷酸探针进行杂交分析(Northern blot),显示性腺激素通过减少编码LH和FSH亚基的mrna的拷贝数发挥作用。使用垂体前叶细胞,在标记蛋氨酸存在下培养,我们证实了我们之前的观察,即GnRH刺激LH多肽链的生物合成。由于LH的释放,这种影响不是继发性的。当在糖基化抑制剂tunicamycin的存在下进行孵育时,它不被抑制。与α相关的多肽的特异性免疫沉淀的sds -聚丙烯酰胺凝胶电泳使我们能够识别出3种不同形式的α多肽:21K(部分糖基化),23K(真实)和25K(高糖基化)。除了刺激LH的释放和合成外,GnRH还刺激α的23K和25K形式的释放。在tunicamycin存在的情况下,检测到在细胞内积累的额外16K形式的载脂蛋白α。cAMP类似物(8-Br-cAMP),细胞内cAMP生成物(choleragen, forskolin)以及二酰基甘油(TPA)类似物模拟GnRH的刺激作用。然而,尽管目前还没有证据表明cAMP或二酰基甘油介导GnRH对LH多肽链生物合成的影响,但我们的数据表明,细胞内磷酸化蛋白在这一过程中起主要作用。
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