Gonadotropin and cAMP modulation of IGE binding protein production in ovarian granulosa cells.

Gonadotropin and cAMP modulation of IGE binding protein production in ovarian granulosa cells.
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DOI:
10.1152/ajpendo.1992.262.4.e497
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发表时间:
1992-04
期刊:
The American journal of physiology
影响因子:
--
通讯作者:
R. Grimes;S. Samaras;J. Barber;S. Shimasaki;N. Ling;J. Hammond
R. Grimes;S. Samaras;J. Barber;S. Shimasaki;N. Ling;J. Hammond
中科院分区:
其他
文献类型:
--
作者:
R. Grimes;S. Samaras;J. Barber;S. Shimasaki;N. Ling;J. Hammond

文献摘要

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猪颗粒细胞(GC)在培养中产生胰岛素样生长因子(IGF)结合蛋白(BP)-3和IGFBP-2。促性腺激素,促卵泡激素(FSH),显着抑制GC生产这些IGFBPs在控制文化和文化刺激胰岛素加表皮生长因子(EGF)或IGF-I加EGF。腺苷酸环化酶刺激剂(毛喉素,霍乱毒素)和腺苷3 ',5'-环一磷酸(cAMP)的衍生物,8-溴腺苷3 ',5'-环一磷酸,以类似于FSH的方式抑制IGFBP的合成。相反,与对照相比,cAMP作用的拮抗剂(R)-p-腺苷3 ',5'-环硫代磷酸酯[(R)-p-cAMPS]显著刺激IGFBP-3和IGFBP-2的产生。(R)-p-cAMPS的这种刺激作用被FSH以剂量依赖性方式共同处理所抵消。最后,用FSH加3-异丁基-1-甲基黄嘌呤处理GC培养物导致IGFBP-3 mRNA编码的细胞含量显著减少,而IGFBP-2 mRNA没有变化。总之,发现升高细胞内cAMP的药物模拟FSH对IGFBP产生的作用。
Porcine granulosa cells (GC) produce insulin-like growth factor (IGF) binding protein (BP)-3 and IGFBP-2 in culture. A gonadotropin, follicle-stimulating hormone (FSH), dramatically inhibited GC production of these IGFBPs in control cultures and in cultures stimulated by insulin plus epidermal growth factor (EGF) or IGF-I plus EGF. Stimulators of adenylate cyclase (forskolin, cholera toxin) and a derivative of adenosine 3',5'-cyclic monophosphate (cAMP), 8-bromoadenosine 3',5'-cyclic monophosphate, inhibited IGFBP synthesis in a manner similar to FSH. In contrast, the antagonist of cAMP action, (R)-p-adenosine 3',5'-cyclic phosphorothioate [(R)-p-cAMPS], significantly stimulated production of IGFBP-3 and IGFBP-2 compared with controls. This stimulatory effect of (R)-p-cAMPS was counteracted by cotreatment with FSH in a dose-dependent manner. Finally, treatment of GC cultures with FSH plus 3-isobutyl-1-methylxanthine resulted in a significant reduction in cellular content of mRNA coding for IGFBP-3 with no change in IGFBP-2 mRNA. In summary, agents that elevate intracellular cAMP were found to mimic the effects of FSH on IGFBP production.