Huang Xiao, Jin Jiewen, Shen Shanmei, Xia Yanjie, Xu Pei, Zou Xiang, Wang Hongwei, Yi Long, Wang Yong, Gao Qian
a State Key Laboratory of Chemistry for Life Science & Jiangsu Key Laboratory of Molecular Medicine, Medical School of Nanjing University , Nanjing , China and.
b Divisions of Endocrinology , The Affiliated Drum Tower Hospital, Medical School, Nanjing University , Nanjing , China.
Gynecol Endocrinol. 2016;32(3):201-5. doi: 10.3109/09513590.2015.1106470. Epub 2015 Nov 3.
The differential steroid production in the theca and granulosa cells in ovary are resulted from unique enzyme expression profiles. Among them, c-fos, a downstream target of mitogen and extracellular signal-regulated kinases (MEK/ERK) signaling, takes part in this compartment. In this study, we investigated the effect of c-fos on the steady-state levels of CYP17 and CYP19 in human ovarian granulosa-like tumor cell line (KGN) by inhibiting MEK/ERK pathway with PD98059. As a result, our finding demonstrated the distinct distribution patterns of CYP17 and CYP19 in KGN. Moreover, the MEK/ERK pathway functions to inhibit the production of CYP17, while enhance the production of CYP19 in granulosa cells, probably involving a c-fos-dependent mechanism. In conclusion, factors such as c-fos may play a crucial role in the down-regulation of CYP17 and up-regulation of CYP19 in granulosa cells, thereby suppressing androstenedione synthesis.
卵巢中膜细胞和颗粒细胞甾体激素产生的差异源于独特的酶表达谱。其中,c-fos作为丝裂原和细胞外信号调节激酶(MEK/ERK)信号通路的下游靶点,参与了这一过程。在本研究中,我们通过用PD98059抑制MEK/ERK通路,研究了c-fos对人卵巢颗粒样肿瘤细胞系(KGN)中CYP17和CYP19稳态水平的影响。结果,我们的发现表明CYP17和CYP19在KGN中具有不同的分布模式。此外,MEK/ERK通路在颗粒细胞中发挥作用,抑制CYP17的产生,同时增强CYP19的产生,这可能涉及一种依赖c-fos的机制。总之,c-fos等因素可能在颗粒细胞中CYP17的下调和CYP19的上调中起关键作用,从而抑制雄烯二酮的合成。