Falender Allison E, Lanz Rainer, Malenfant Daniel, Belanger Luc, Richards JoAnne S
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Endocrinology. 2003 Aug;144(8):3598-610. doi: 10.1210/en.2002-0137.
Steroidogenic factor-1 (SF-1) (NR5A1) is an orphan nuclear receptor that plays a premier role in ovarian organogenesis. Recent studies document mRNA expression of the structurally related factor NR5A2 (FTF, LRH-1, SF-2) in the adult ovary and more specifically in granulosa cells and luteal cells but not theca cells. Conversely, SF-1 was shown to be expressed at higher levels in theca/interstitial cells. These latter observations raised the possibility that FTF/LRH-1 may control target gene expression in granulosa cells of developing follicles. Using quantitative PCR our results show that FTF/LRH-1 message is expressed at higher levels in the ovary than in liver or other tissues analyzed. We show by in situ hybridization and LacZ expression in ovaries of transgenic mice bearing an FTF-promoter-LacZ fusion gene that FTF/LRH-1 is selectively expressed in granulosa cells of rat and mouse ovaries and is not present in theca cells or interstitial cells. However, by a variety of approaches, we showed that SF-1 mRNA and protein are expressed in greater amounts than FTF/LRH-1 in granulosa cells of follicles at all stages of development. Expression of SF-1 mRNA and protein in granulosa cells was verified by in situ hybridization, immunohistochemistry of ovarian sections, and immunocytochemistry of cultured rat granulosa cells. The significance of SF-1 in regulating target gene activation was supported by EMSA. An abundant granulosa cell protein binding to the SF-1-binding motif (CCAAGGTCA) present in the aromatase promoter and an FTF/LRH-1 motif (TGTCCTTGAACA) in the alpha-fetoprotein promoter was supershifted by two SF-1-specific antibodies but not by an FTF antibody. Conversely, with the same probes, a less abundant protein/DNA complex present in liver and ovarian cell extracts was shifted by an FTF antibody but not by the SF-1 antibodies. SF-1 and FTF/LRH-1 were differentially regulated in vivo by estradiol, FSH and prolactin. Collectively these data indicate that granulosa cells of small and preovulatory follicles express both SF-1 and FTF/LRH-1 and that each orphan receptor may regulate target gene expression in these cells.
类固醇生成因子-1(SF-1)(NR5A1)是一种孤儿核受体,在卵巢器官发生过程中起主要作用。最近的研究记录了结构相关因子NR5A2(FTF、LRH-1、SF-2)在成年卵巢中的mRNA表达,更具体地说是在颗粒细胞和黄体细胞中表达,而在卵泡膜细胞中不表达。相反,SF-1在卵泡膜/间质细胞中的表达水平较高。这些观察结果提出了一种可能性,即FTF/LRH-1可能控制发育中卵泡颗粒细胞中的靶基因表达。通过定量PCR,我们的结果表明,FTF/LRH-1信息在卵巢中的表达水平高于肝脏或其他分析组织。我们通过原位杂交以及在携带FTF-启动子-LacZ融合基因的转基因小鼠卵巢中的LacZ表达表明,FTF/LRH-1在大鼠和小鼠卵巢的颗粒细胞中选择性表达,而不存在于卵泡膜细胞或间质细胞中。然而,通过多种方法,我们发现,在卵泡发育的各个阶段,颗粒细胞中SF-1的mRNA和蛋白表达量均高于FTF/LRH-1。通过原位杂交、卵巢切片免疫组织化学以及培养的大鼠颗粒细胞免疫细胞化学验证了颗粒细胞中SF-1 mRNA和蛋白的表达。电泳迁移率变动分析(EMSA)支持了SF-1在调节靶基因激活中的重要性。两种SF-1特异性抗体可使一种与芳香化酶启动子中存在的SF-1结合基序(CCAAGGTCA)以及甲胎蛋白启动子中的FTF/LRH-1基序(TGTCCTTGAACA)结合的丰富颗粒细胞蛋白发生超迁移,而FTF抗体则不能。相反,使用相同的探针,一种在肝脏和卵巢细胞提取物中存在的丰度较低的蛋白/DNA复合物可被FTF抗体迁移,而不能被SF-1抗体迁移。SF-1和FTF/LRH-1在体内受到雌二醇、促卵泡激素(FSH)和催乳素的差异调节。这些数据共同表明,小卵泡和排卵前卵泡的颗粒细胞同时表达SF-1和FTF/LRH-1,并且每种孤儿受体可能在这些细胞中调节靶基因表达。