Huang Shuo, Pang Yanli, Yan Jie, Lin Shengli, Zhao Yue, Lei Li, Yan Liying, Li Rong, Ma Caihong, Qiao Jie
Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China.
Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing, China.
Sci Rep. 2016 Jul 8;6:26205. doi: 10.1038/srep26205.
Low progesterone levels are associated with luteal phase deficiency in women with polycystic ovary syndrome (PCOS). The mechanisms regulating progesterone biosynthesis in the granulosa cells from women with PCOS is largely unknown. Fractalkine is expressed in human ovaries, and is reported to regulate progesterone production in granulosa cells of healthy women. In the current study, we aimed to examine the role of fractalkine in women with PCOS. Reduced fractalkine levels were found in follicular fluid and granulosa cells, accompanied by decreased progesterone production and reduced steroidogenic acute regulatory protein (StAR) expression in the granulosa cells of patients with PCOS. Administration of fractalkine reversed the inhibition of progesterone and StAR expression. The mechanism mediating these effects may be associated with the inhibition of ERK activity in the granulosa cells from women with PCOS. Our findings revealed that fractalkine regulated steroidogenesis in follicular granulosa cells of women with PCOS.
孕酮水平低与多囊卵巢综合征(PCOS)女性的黄体期缺陷有关。PCOS女性颗粒细胞中调节孕酮生物合成的机制在很大程度上尚不清楚。趋化因子在人卵巢中表达,据报道其可调节健康女性颗粒细胞中的孕酮生成。在本研究中,我们旨在研究趋化因子在PCOS女性中的作用。在PCOS患者的卵泡液和颗粒细胞中发现趋化因子水平降低,同时伴有孕酮生成减少和颗粒细胞中类固醇生成急性调节蛋白(StAR)表达降低。给予趋化因子可逆转对孕酮和StAR表达的抑制。介导这些效应的机制可能与PCOS女性颗粒细胞中ERK活性的抑制有关。我们的研究结果表明,趋化因子调节PCOS女性卵泡颗粒细胞中的类固醇生成。