Jayes F C, Day R N, Garmey J C, Urban R J, Zhang G, Veldhuis J D
Department of Internal Medicine, NIH Specialized Cooperative Center in Reproduction Research, University of Virginia Health Sciences Center, Charlottesville 22908, USA.
Endocrinology. 2000 Jul;141(7):2377-84. doi: 10.1210/endo.141.7.7558.
Given the evident modulation of FSH-induced steroidogenesis by Ca2+ in granulosa cells, we here test the hypothesis that Ca2+ controls expression of the enzymatically rate-limiting cytochrome P450(scc) (CYP11A) gene. To test this postulate, we quantitated the ability of Ca2+ to regulate: 1) transcriptional activity of a transiently transfected luciferase reporter gene driven by a 2.32-kb 5'-upstream fragment of the porcine P450(scc) gene promoter region; and 2) accumulation of endogenous P450(scc) transcripts in primary monolayer cultures of porcine granulosa cells. To this end, granulosa cells were stimulated for 4 h with FSH (15 ng/ml, NIDDK-oFSH-20) or 8-Bromo-cAMP (8 Br-cAMP, 1 mM) in serum-free medium containing either 1.8 mM Ca2- or no added Ca2+ with 100 microM EGTA or 100 microM CoCl2. In the presence of extracellular Ca2+, FSH and 8 Br-cAMP stimulated expression of the transfected P450(scc) promoter-reporter fusion construct by 5.6 +/- 1.1 and 3.6 +/- 0.67-fold, respectively over Ca2+-containing unstimulated control (P < or = 0.04, n = 5-6 experiments). The foregoing two agonists augmented 4-h progesterone production by cultured granulosa cells by 1.8 +/- 0.11 and 1.6 +/- 0.16-fold, respectively (P < or = 0.001 for FSH and P < or = 0.01 for 8 Br-cAMP). FSH and 8 Br-cAMP also significantly elevated endogenous P450(scc) transcript levels as measured by homologous solution-hybridization RNase protection assay; i.e. by 3.1 +/- 0.49 and 2.9 +/- 0.45-fold, respectively (P < or = 0.001). In Ca2+-free/EGTA-supplemented medium, basal luciferase reporter-gene activity and endogenous P450(scc) messenger RNA accumulation in granulosa cells declined to 34 +/- 12% and 78 +/- 12%, respectively, of corresponding values in control (unstimulated Ca2+-containing) cultures. Extracellular Ca2+ deprivation inhibited the stimulatory effect of FSH (and 8 Br-cAMP) on P450(scc) promoter-luciferase reporter expression to 58 +/- 30% (and 58 +/- 23%), and restrained endogenous P450(scc) message accumulation to 86 +/- 15% (and 96 +/- 18%) of the value in Ca2+-containing control. Extracellular Ca2+ withdrawal suppressed FSH (and 8 Br-cAMP)-driven progesterone production over 4 h to basal levels but did not alter FSH-stimulated cAMP accumulation by granulosa cells. Ca2+-deprived cells exposed to serum-containing media regained P450(scc) responsiveness to both agonists. Antagonism of cellular uptake of Ca2+ and other divalent cations via administration of cobalt chloride (100 microM) inhibited FSH and 8 Br-cAMP's stimulation of endogenous (but not exogenous promoter-driven) P450(scc) gene expression. In contrast, granulosa-cell concentrations of messenger RNA's encoding sterol-carrier protein-2 (SCP-2) and the low density lipoprotein receptor were not altered by Ca2+ withdrawal. In summary, uptake of extracellular Ca2+ by porcine granulosa cells significantly potentiates transactivation of the endogenously expressed and exogenously transfected P450(scc) gene by FSH and 8 Br-cAMP. The agonistic impact of Ca2+ on P450(scc) promoter activity is requisite downstream of FSH-induced cAMP second-messenger signaling.
鉴于颗粒细胞中Ca2+对促卵泡激素(FSH)诱导的类固醇生成有明显调节作用,我们在此检验Ca2+控制限速酶细胞色素P450(scc)(CYP11A)基因表达这一假说。为验证这一假设,我们对Ca2+调节以下方面的能力进行了定量分析:1)由猪P450(scc)基因启动子区域2.32 kb的5'上游片段驱动的瞬时转染荧光素酶报告基因的转录活性;2)猪颗粒细胞原代单层培养物中内源性P450(scc)转录本的积累。为此,在含有1.8 mM Ca2+或不添加Ca2+(添加100 microM乙二醇双四乙酸(EGTA)或100 microM氯化钴(CoCl2))的无血清培养基中,用FSH(15 ng/ml,NIDDK - oFSH - 20)或8 - 溴环磷酸腺苷(8 Br - cAMP,1 mM)刺激颗粒细胞4小时。在细胞外Ca2+存在的情况下,FSH和8 Br - cAMP分别使转染的P450(scc)启动子 - 报告基因融合构建体的表达比含Ca2+的未刺激对照提高了5.6±1.1倍和3.6±0.67倍(P≤0.04,n = 5 - 6次实验)。上述两种激动剂分别使培养的颗粒细胞4小时孕酮产量增加了1.8±0.11倍和1.6±0.16倍(FSH的P≤0.001,8 Br - cAMP的P≤0.01)。通过同源溶液杂交核糖核酸酶保护分析测定,FSH和8 Br - cAMP也显著提高了内源性P450(scc)转录本水平;即分别提高了3.1±0.49倍和2.9±0.45倍(P≤0.001)。在无Ca2+/添加EGTA的培养基中,颗粒细胞中基础荧光素酶报告基因活性和内源性P450(scc)信使核糖核酸积累分别降至对照(含Ca2+未刺激)培养物相应值的34±12%和78±12%。细胞外Ca2+剥夺将FSH(和8 Br - cAMP)对P450(scc)启动子 - 荧光素酶报告基因表达的刺激作用抑制至58±30%(和58±23%),并将内源性P450(scc)信使积累抑制至含Ca2+对照值的86±15%(和96±18%)。细胞外Ca2+撤除将FSH(和8 Br - cAMP)驱动的4小时孕酮产量抑制至基础水平,但未改变FSH刺激的颗粒细胞中环磷酸腺苷积累。暴露于含血清培养基中的Ca2+剥夺细胞恢复了对两种激动剂的P450(scc)反应性。通过给予氯化钴(100 microM)拮抗细胞对Ca2+和其他二价阳离子的摄取,抑制了FSH和8 Br - cAMP对内源性(但非外源性启动子驱动)P450(scc)基因表达的刺激。相反,编码固醇载体蛋白 - 2(SCP - 2)和低密度脂蛋白受体的信使核糖核酸的颗粒细胞浓度未因Ca2+撤除而改变。总之,猪颗粒细胞摄取细胞外Ca2+显著增强了FSH和8 Br - cAMP对内源性表达和外源性转染的P450(scc)基因的反式激活。Ca2+对P450(scc)启动子活性的激动作用是FSH诱导的环磷酸腺苷第二信使信号传导下游所必需的。