首页> 外文期刊>Molecular and Cellular Endocrinology >Growth factors and phorbol-12-myristate-13-acetate modulate the follicle-stimulating hormone- and cyclic adenosine-3',5'-monophosphate-dependent regulation of 17beta-hydroxysteroid dehydrogenase type 1 expression in rat granulosa cells.
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Growth factors and phorbol-12-myristate-13-acetate modulate the follicle-stimulating hormone- and cyclic adenosine-3',5'-monophosphate-dependent regulation of 17beta-hydroxysteroid dehydrogenase type 1 expression in rat granulosa cells.

机译:生长因子和佛波醇12-肉豆蔻酸酯13-乙酸酯调节大鼠颗粒细胞中17β-羟类固醇脱氢酶1型表达的刺激卵泡的激素和环状腺苷3',5'-单磷酸酯依赖性调节。

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摘要

In the present study primary cultures of rat granulosa cells obtained from diethylstilbestrol (DES)-primed immature rats were used to study the regulation of 17beta-hydroxysteroid dehydrogenase (17HSD) activity and type 1 expression via protein kinase A (PKA)- and C (PKC)-dependent pathways, and by several autocrine and/or paracrine growth factors. Follicle-stimulating hormone (FSH), 8-bromo-cyclic adenosine-3',5'-monophosphate (8-Br-cAMP) and transforming growth factor beta1 (TGFbeta1) strongly enhanced 17HSD activity and type 1 expression. The stimulatory effects of FSH and 8-Br-cAMP were further potentiated by TGFbeta1. In contrast, neither phorbol-12-myristate-13-acetate (PMA), epidermal growth factor (EGF), transforming growth factor alpha (TGFalpha) nor fibroblast growth factor (bFGF) affected 17HSD activity or type 1 expression when given alone. However, they effectively neutralized the stimulatory effects of 8-Br-cAMP and FSH. The present data suggest that, in rat granulosa cells 17HSD type 1 expression is primarily induced by FSH acting via PKA-dependent pathway and the extent of the induction is modulated by PKC-dependent inhibition and autocrine/paracrine growth factors present in the ovary.
机译:在本研究中,从己烯雌酚(DES)引发的未成熟大鼠获得的大鼠颗粒细胞的原代培养用于研究17β-羟基类固醇脱氢酶(17HSD)活性的调节以及通过蛋白激酶A(PKA)-和C的1型表达( PKC)依赖的途径,以及几种自分泌和/或旁分泌生长因子。促卵泡激素(FSH),8-溴环腺苷3',5'-单磷酸(8-Br-cAMP)和转化生长因子beta1(TGFbeta1)大大增强了17HSD活性和1型表达。 TGFbeta1进一步增强了FSH和8-Br-cAMP的刺激作用。相反,单独给予时,佛波12-肉豆蔻13-乙酸(PMA),表皮生长因子(EGF),转化生长因子α(TGFalpha)或成纤维细胞生长因子(bFGF)均不影响17HSD活性或1型表达。但是,它们有效地中和了8-Br-cAMP和FSH的刺激作用。目前的数据表明,在大鼠颗粒细胞中,17HSD 1型表达主要受FSH通过PKA依赖性途径的作用诱导,诱导程度受PKC依赖性抑制作用和卵巢中存在的自分泌/旁分泌生长因子调节。

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