Breen Kellie M, Thackray Varykina G, Hsu Tracy, Mak-McCully Rachel A, Coss Djurdjica, Mellon Pamela L
Department of Reproductive Medicine/Neuroscience, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093-0674, USA.
Mol Endocrinol. 2012 Oct;26(10):1716-31. doi: 10.1210/me.2011-1327. Epub 2012 Jul 31.
Increased glucocorticoid secretion is a common response to stress and has been implicated as a mediator of reproductive suppression upon the pituitary gland. We utilized complementary in vitro and in vivo approaches in the mouse to investigate the role of glucocorticoids as a stress-induced intermediate capable of gonadotrope suppression. Repeated daily restraint stress lengthened the ovulatory cycle of female mice and acutely reduced GnRH-induced LH secretion and synthesis of LH β-subunit (LHβ) mRNA, coincident with increased circulating glucocorticoids. Administration of a stress level of glucocorticoid, in the absence of stress, blunted LH secretion in ovariectomized female mice, demonstrating direct impairment of reproductive function by glucocorticoids. Supporting a pituitary action, glucocorticoid receptor (GR) is expressed in mouse gonadotropes and treatment with glucocorticoids reduces GnRH-induced LHβ expression in immortalized mouse gonadotrope cells. Analyses revealed that glucocorticoid repression localizes to a region of the LHβ proximal promoter, which contains early growth response factor 1 (Egr1) and steroidogenic factor 1 sites critical for GnRH induction. GR is recruited to this promoter region in the presence of GnRH, but not by dexamethasone alone, confirming the necessity of the GnRH response for GR repression. In lieu of GnRH, Egr1 induction is sufficient for glucocorticoid repression of LHβ expression, which occurs via GR acting in a DNA- and dimerization-independent manner. Collectively, these results expose the gonadotrope as an important neuroendocrine site impaired during stress, by revealing a molecular mechanism involving Egr1 as a critical integrator of complex formation on the LHβ promoter during GnRH induction and GR repression.
糖皮质激素分泌增加是对压力的常见反应,并且被认为是垂体生殖抑制的介质。我们利用小鼠体内外互补的方法来研究糖皮质激素作为应激诱导的能够抑制促性腺激素细胞的中间介质的作用。每天重复的束缚应激延长了雌性小鼠的排卵周期,并急性降低了GnRH诱导的LH分泌以及LHβ亚基(LHβ)mRNA的合成,同时循环糖皮质激素增加。在无应激情况下给予应激水平的糖皮质激素,会使去卵巢雌性小鼠的LH分泌减弱,这表明糖皮质激素对生殖功能有直接损害。支持垂体作用的是,糖皮质激素受体(GR)在小鼠促性腺激素细胞中表达,并且用糖皮质激素处理会降低永生化小鼠促性腺激素细胞中GnRH诱导的LHβ表达。分析表明,糖皮质激素的抑制作用定位于LHβ近端启动子区域,该区域包含对GnRH诱导至关重要的早期生长反应因子1(Egr1)和类固醇生成因子1位点。在有GnRH存在的情况下,GR会被募集到该启动子区域,但单独使用地塞米松则不会,这证实了GnRH反应对于GR抑制的必要性。在没有GnRH的情况下,Egr1的诱导足以使糖皮质激素抑制LHβ表达,这是通过GR以不依赖DNA和二聚化的方式发挥作用而发生的。总的来说,这些结果揭示了促性腺激素细胞是应激期间受损的重要神经内分泌位点,通过揭示一种分子机制,即Egr1作为GnRH诱导和GR抑制过程中LHβ启动子上复合物形成的关键整合因子。