Reproductive Medicine Center, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, People's Republic of China.
PLoS One. 2012;7(6):e39950. doi: 10.1371/journal.pone.0039950. Epub 2012 Jun 28.
The androgen receptor (AR) is a nuclear receptor that is expressed in growing follicles and involved in folliculogenesis and follicle growth. The orphan nuclear receptor, Nur77, also has an important role in steroid signaling and follicle maturation. We hypothesized that AR levels and androgen signaling through AR are regulated by Nur77 in the ovary. In the ovaries of Nur77 knockout mice (n = 5), real-time PCR results showed that the mRNA levels of AR and an androgen signaling target gene, Kitl, were decreased by 35% and 24%, respectively, relative to wild-type mice (n = 5), which suggested transcriptional regulation of AR by Nur77 in vivo. In cultured mouse granulosa cells and a steroidogenic human ovarian granulosa-like tumor cell line, KGN, mRNA and protein expression levels of AR were increased by overexpressing Nur77 but decreased by knocking down endogenous Nur77. Consistent with increased AR expression, chromatin immunoprecipitation showed that Nur77 bound to the NGFI-B response element (NBRE) in the AR promoter sequence. AR promoter activity was stimulated by Nur77 in HEK293T cells and attenuated in Nur77 knockout mouse granulosa cells (luciferase assay). Overexpression of Nur77 enhanced the androgenic induction of Kitl (200 nM; 48h), while knockout of Nur77 attenuated this induction. These results demonstrate that AR is regulated by Nur77 in the ovaries, and they suggest that the participation of Nur77 in androgen signaling may be essential for normal follicular development.
雄激素受体(AR)是一种核受体,在生长卵泡中表达,并参与卵泡发生和卵泡生长。孤儿核受体 Nur77 也在类固醇信号转导和卵泡成熟中发挥重要作用。我们假设 AR 水平和通过 AR 的雄激素信号转导受卵巢中 Nur77 的调节。在 Nur77 敲除小鼠(n=5)的卵巢中,实时 PCR 结果显示,AR 和雄激素信号靶基因 Kitl 的 mRNA 水平分别降低了 35%和 24%,与野生型小鼠(n=5)相比,这表明 Nur77 在体内对 AR 进行转录调节。在培养的小鼠颗粒细胞和类固醇生成的人卵巢颗粒样肿瘤细胞系 KGN 中,过表达 Nur77 可增加 AR 的 mRNA 和蛋白表达水平,而敲低内源性 Nur77 则降低 AR 的表达水平。与 AR 表达增加一致,染色质免疫沉淀显示 Nur77 结合到 AR 启动子序列中的 NGFI-B 反应元件(NBRE)上。Nur77 在 HEK293T 细胞中刺激 AR 启动子活性,并在 Nur77 敲除小鼠颗粒细胞中减弱(荧光素酶测定)。Nur77 的过表达增强了 Kitl 的雄激素诱导(200 nM;48h),而 Nur77 的敲除则减弱了这种诱导。这些结果表明 AR 在卵巢中受 Nur77 调节,并且表明 Nur77 参与雄激素信号转导对于正常卵泡发育可能是必需的。