Inhibin A inhibits follicle-stimulating hormone (FSH) action by suppressing its receptor expression in cultured rat granulosa cells

被引:36
|
作者
Lu, Cuiling [1 ,2 ]
Yang, Wei [1 ]
Chen, Min [1 ]
Liu, Tao [1 ]
Yang, Junling [1 ]
Tan, Ping [1 ]
Li, Lei [1 ]
Hu, Xiaoqian [1 ]
Fan, Cuihong [1 ]
Hu, Zhaoyuan [1 ]
Liu, Yixun [1 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Reprod Biol, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
关键词
Inhibin A; FSH; FSHR; Granulosa cells; RECOMBINANT HUMAN INHIBIN; ACTIVATED PROTEIN-KINASE; RIBONUCLEIC-ACID LEVELS; CORPUS-LUTEUM FUNCTION; ANDROGEN RECEPTOR; GENE-EXPRESSION; ACTIVIN-A; STEROIDOGENIC FACTOR-1; FACTOR-I; E-BOX;
D O I
10.1016/j.mce.2008.09.039
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inhibin has long been considered as a suppresser of follicle-stimulating hormone (FSH) secretion from anterior pituitary through pituitary-gonad negative feedback to regulate follicle development. We demonstrated that addition of inhibin A could significantly suppress FSH-induced FSHR mRNA level in cultured rat granulosa cells (GCs) measured by real-time PCR. The inhibin A exerted its action mainly by inhibiting FSHR promoter activity. Furthermore, exogenous inhibin A could dramatically decrease FSH-induced P450arom and P450scc level and suppress progesterone and estradiol production in the cultured GCs, but it did not decrease forskolin-induced steroidogenesis. indicating that the inhibitory effect of inhibin A on FSH action may be upstream of cAMP signaling. Inhibin A was also capable of suppressing FSH-induced expression of steroidogenic factor 1 (SF-1) and androgen receptor, but stimulating DAX-1 expression in the culture. Our study has provided new evidence to show that inhibin A is capable of feedback antagonizing FSH action on GCs by reducing FSHR expression at ovarian level via a short feedback loop. Transcriptional factor receptors, such as SF-1, AR and DAX-1 were involved in this regulation. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:48 / 56
页数:9
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