Fu Yun-Xing, Wang Fei-Miao, Ou-Yang Xiao-E, Yang Hui-Min, Hu Ting, Wang Ya-Fei, Wang Yan-Fei, Wang Hui, Hu Rong
Ningxia Medical University, General Hospital of Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Reproductive Medicine Center, General Hospital of Ningxia Medical University, Key Laboratory of Fertility Preservation and Maintenance of Ministry of Education, Ningxia Medical University, Yinchuan, 750004, Ningxia, China.
Reprod Sci. 2020 Jan;27(1):325-333. doi: 10.1007/s43032-019-00033-4. Epub 2020 Jan 1.
Anti-Müllerian hormone (AMH) downregulates the level of stem cell factor (SCF) via the cAMP/PKA signaling pathway in human granulosa cells (GCs). Little information is available on the molecular mechanism underlying the interaction. This study is aimed at determining whether AMH regulates expression of SCF via the cAMP-PKA-CREB signaling pathway in human GCs. In the present study, we verified the binding of cAMP-response element-binding protein (CREB) to promoter of SCF in human GCs. Furthermore, the effect of CREB was tested on the SCF promoter, and the site of CREB binding to SCF promoter was identified using truncations as well as assays of SCF-promoted mutation and CREB mutation. To investigate the correlation among AMH, SCF promoter, and CREB, pGL-Basic-SCF+CREB was transfected into overexpressed AMH GCs (AMH-high GCs), low expressed AMH GCs (AMH-low GCs), and normal GCs (GCs), respectively. Finally, immunofluorescence, double immunostaining, and Western blot were carried out in AMH-high and AMH-low GCs to confirm the AMH-mediated regulation of SCF expression by inhibiting the phosphorylation of CREB (pCREB) in GCs. Results indicated CREB interacted with SCF promoter and significantly enhanced the transcription level of SCF. The CREB binding site was localized at 318-321 bp of SCF gene promote. AMH inhibits the expression of SCF by phosphorylation of CREB via the PKA signaling pathway in GCs. These findings provide an in-depth understanding of the molecular mechanism underlying AMH suppressing the follicle growth, which would aid in the development of a novel therapy.
抗苗勒管激素(AMH)通过环磷酸腺苷/蛋白激酶A(cAMP/PKA)信号通路下调人颗粒细胞(GCs)中干细胞因子(SCF)的水平。关于这种相互作用的分子机制,目前所知甚少。本研究旨在确定AMH是否通过cAMP-PKA-CREB信号通路调节人颗粒细胞中SCF的表达。在本研究中,我们验证了cAMP反应元件结合蛋白(CREB)与人颗粒细胞中SCF启动子的结合。此外,检测了CREB对SCF启动子的作用,并通过截短以及SCF启动子突变和CREB突变分析确定了CREB与SCF启动子的结合位点。为了研究AMH、SCF启动子和CREB之间的相关性,将pGL-Basic-SCF+CREB分别转染到AMH过表达颗粒细胞(AMH高颗粒细胞)、AMH低表达颗粒细胞(AMH低颗粒细胞)和正常颗粒细胞(颗粒细胞)中。最后,在AMH高和AMH低颗粒细胞中进行免疫荧光、双重免疫染色和蛋白质印迹,以证实AMH通过抑制颗粒细胞中CREB(pCREB)的磷酸化介导对SCF表达的调节。结果表明,CREB与SCF启动子相互作用并显著提高了SCF的转录水平。CREB结合位点位于SCF基因启动子的318-321bp处。AMH通过PKA信号通路使CREB磷酸化,从而抑制颗粒细胞中SCF的表达。这些发现为深入了解AMH抑制卵泡生长的分子机制提供了依据,这将有助于开发新的治疗方法。