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转化生长因子-α可减弱培养的大鼠颗粒细胞芳香化酶活性的获得。

Transforming growth factor-alpha attenuates the acquisition of aromatase activity by cultured rat granulosa cells.

作者信息

Adashi E Y, Resnick C E, Twardzik D R

出版信息

J Cell Biochem. 1987 Jan;33(1):1-13. doi: 10.1002/jcb.240330102.

DOI:10.1002/jcb.240330102
PMID:3029149
Abstract

The effect of transforming growth factor-alpha (TGF alpha) on granulosa cell differentiation, as assessed by the acquisition of aromatase activity, was evaluated in vitro by using a primary culture of rat granulosa cells. Harvested from immature, diethylstilbestrol-treated rats, granulosa cells were cultured under serum-free conditions for 72 hr in the presence of saturating concentrations (10(-7)M) of aromatase substrate androstenedione with or without the specific experimental agents. Basal aromatase activity, as assessed by the generation of radioimmunoassayable estrogen was negligible, remaining unaffected by treatment with TGF alpha (10 ng/ml) by itself. Whereas treatment with follicle-stimulating hormone (FSH) resulted in a substantial increase in the extent of aromatization, concurrent treatment with TGF alpha (10 ng/ml) resulted in significant (P less than 0.05), yet reversible inhibition (78 +/- 5.6%) of FSH action. Significantly, this effect of TGF alpha could not be accounted for by a decrease in cellular viability or plating efficiency nor by a decrease in the number of cells or their DNA content. Although independent of the FSH dose employed, the TGF alpha effect proved dose- and time-dependent, with an apparent median inhibitory dose (EC50) of 0.33 +/- 0.04 ng/ml, and a minimal time requirement of 48 hr. Capable of substantial inhibition of the forskolin-stimulated accumulation of extracellular adenosine 3', 5' cyclic monophosphate (cAMP) and estrogen, TGF alpha had a measurable albeit limited effect on N6, 2-'O-Dibutyryladenosine 3':5'-cyclic monophosphate-supported estrogen production. Relative potency comparison revealed epidermal growth factor (EGF; EC50 = 0.24 +/- 0.03 ng/ml) and TGF alpha to be virtually equipotent as regards the attenuation of FSH-stimulated estrogen biosynthesis. Taken together, our findings indicate that TGF alpha, like EGF, acting at subnanomolar concentrations, is capable of attenuating the FSH-stimulated (but not basal) accumulation of estrogen. This effect of TGF alpha proved time- and dose-dependent, involving virtually complete neutralization of FSH action at site(s) both proximal and distal to cAMP generation. As such, these findings provide yet another example of the remarkable qualitative and quantitative similarities between EGF and TGF alpha, thereby reaffirming the prospect that ligands of the EGF/TGF alpha receptor may play a modulatory role in the course of granulosa cell ontogeny.

摘要

利用大鼠颗粒细胞原代培养物在体外评估了转化生长因子α(TGFα)对颗粒细胞分化的影响,该影响通过芳香化酶活性的获得来评估。颗粒细胞从用己烯雌酚处理的未成熟大鼠中获取,在无血清条件下,于饱和浓度(10⁻⁷M)的芳香化酶底物雄烯二酮存在下,培养72小时,同时添加或不添加特定实验试剂。通过放射免疫分析法可检测到的雌激素生成量评估,基础芳香化酶活性可忽略不计,单独用TGFα(10 ng/ml)处理对其无影响。而用促卵泡激素(FSH)处理导致芳香化程度大幅增加,同时用TGFα(10 ng/ml)处理则导致FSH作用受到显著(P<0.05)但可逆的抑制(78±5.6%)。重要的是,TGFα的这种作用不能用细胞活力或接种效率的降低、细胞数量或其DNA含量的减少来解释。尽管与所用FSH剂量无关,但TGFα的作用证明具有剂量和时间依赖性,其表观半数抑制剂量(EC50)为0.33±0.04 ng/ml,最短作用时间为48小时。TGFα能够显著抑制福斯可林刺激的细胞外3',5'-环磷酸腺苷(cAMP)和雌激素的积累,对N6,2'-O-二丁酰腺苷3':5'-环磷酸腺苷支持的雌激素生成有可测量但有限的影响。相对效价比较显示,表皮生长因子(EGF;EC50 = 0.24±0.03 ng/ml)和TGFα在减弱FSH刺激的雌激素生物合成方面几乎具有同等效力。综上所述,我们的研究结果表明,TGFα与EGF一样,在亚纳摩尔浓度下起作用,能够减弱FSH刺激(而非基础)的雌激素积累。TGFα的这种作用证明具有时间和剂量依赖性,涉及在cAMP生成近端和远端位点对FSH作用的几乎完全中和。因此,这些研究结果再次提供了EGF和TGFα之间显著的定性和定量相似性的另一个例子,从而再次肯定了EGF/TGFα受体配体可能在颗粒细胞个体发育过程中发挥调节作用的前景。

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Transforming growth factor-alpha attenuates the acquisition of aromatase activity by cultured rat granulosa cells.转化生长因子-α可减弱培养的大鼠颗粒细胞芳香化酶活性的获得。
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