Li Xin, Pishdari Bano, Cui Peng, Hu Min, Yang Hong-Ping, Guo Yan-Rong, Jiang Hong-Yuan, Feng Yi, Billig Håkan, Shao Ruijin
1. Department of Physiology/Endocrinology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. ; 2. Department of Gynecology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China; ; 3. Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Shanghai, China;
1. Department of Physiology/Endocrinology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Int J Biol Sci. 2015 Nov 1;11(12):1376-89. doi: 10.7150/ijbs.13109. eCollection 2015.
The failure of reproductive success in polycystic ovary syndrome (PCOS) patients could be in part due to endometrial dysfunction. However, no studies have investigated any causality between androgen, androgen receptor (AR) expression, and adenosine monophosphate activated protein kinase (AMPK) activation in the endometrium under physiological and pathological conditions. In the present study, we show that 1) endometrial AR expression levels fluctuate in non-PCOS and PCOS patients during the menstrual cycle; 2) the menstrual phase-dependent alteration of p-AMPKα expression occurs in non-PCOS patients but not in PCOS patients; 3) AR expression is higher in PCOS patients than non-PCOS patients during hyperplasia while AMPKα activation (indicated by the ratio of p-AMPKα to AMPKα); and 4) co-localization of AR and Ki-67 in epithelial cell nuclei is observed in endometrial hyperplasia. Importantly, using in vitro human tissue culture and an in vivo 5α-dihydrotestosterone-treated rat model, we show that the action of androgen on AMPKα activation is likely mediated through nuclear AR, especially in epithelial cells. Collectively, we present evidence that AR expression and AMPKα activation depend on menstrual cycle phase and the presence of PCOS, and the data suggest that AR-mediated regulation of AMPKα activation might play a role in the development of endometrial hyperplasia.
多囊卵巢综合征(PCOS)患者生殖成功的失败可能部分归因于子宫内膜功能障碍。然而,尚无研究调查在生理和病理条件下,雄激素、雄激素受体(AR)表达与子宫内膜中腺苷单磷酸活化蛋白激酶(AMPK)激活之间的因果关系。在本研究中,我们发现:1)在月经周期中,非PCOS和PCOS患者的子宫内膜AR表达水平会发生波动;2)非PCOS患者会出现p-AMPKα表达的月经周期依赖性改变,而PCOS患者则不会;3)在增生期,PCOS患者的AR表达高于非PCOS患者,而AMPKα激活(以p-AMPKα与AMPKα的比值表示)情况则相反;4)在子宫内膜增生中观察到上皮细胞核内AR与Ki-67的共定位。重要的是,通过体外人体组织培养和体内5α-双氢睾酮处理的大鼠模型,我们发现雄激素对AMPKα激活的作用可能是通过核AR介导的,尤其是在上皮细胞中。总体而言,我们提供的证据表明,AR表达和AMPKα激活取决于月经周期阶段和PCOS的存在,数据表明AR介导的AMPKα激活调节可能在子宫内膜增生的发展中起作用。