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促黄体生成素通过涉及猕猴黄体中类固醇生成因子-1和β-连环蛋白的多种信号通路调节抑制素α亚基的表达。

Luteinizing hormone regulates inhibin-α subunit expression through multiple signaling pathways involving steroidogenic factor-1 and beta-catenin in the macaque corpus luteum.

作者信息

Suresh Padmanaban S, Medhamurthy Rudraiah

机构信息

Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore 560012, India.

出版信息

Growth Factors. 2012 Jun;30(3):192-206. doi: 10.3109/08977194.2012.678844.

Abstract

We employed different experimental model systems to define the role of GATA4, beta-catenin, and steroidogenic factor (SF-1) transcriptional factors in the regulation of monkey luteal inhibin secretion. Reverse transcription polymerase chain reactions and western blotting analyses show high expression of inhibin-α, GATA4, and beta-catenin in corpus luteum (CL) of the mid-luteal phase. Gonadotropin-releasing hormone receptor antagonist-induced luteolysis model suggested the significance of luteinizing hormone (LH) in regulating these transcriptional factors. Inducible cyclic AMP early repressor mRNA expression was detected in the CL and no change was observed in different stages of CL. Following amino acid sequence analysis, interaction between SF-1 and beta-catenin in mid-stage CL was verified by reciprocal co-immunoprecipitation experiments coupled to immunoblot analysis. Electrophoretic mobility shift analysis support the role of SF-1 in regulating luteal inhibin-α expression. Our results suggest a possible multiple crosstalk of Wnt, cAMP, and SF-1 in the regulation of luteal inhibin secretion.

摘要

我们采用了不同的实验模型系统来确定GATA4、β-连环蛋白和类固醇生成因子(SF-1)转录因子在调节猴黄体抑制素分泌中的作用。逆转录聚合酶链反应和蛋白质印迹分析表明,抑制素-α、GATA4和β-连环蛋白在黄体中期的黄体(CL)中高表达。促性腺激素释放激素受体拮抗剂诱导的黄体溶解模型表明促黄体生成素(LH)在调节这些转录因子中的重要性。在CL中检测到诱导型环磷酸腺苷早期阻遏物mRNA表达,且在CL的不同阶段未观察到变化。经过氨基酸序列分析后,通过相互免疫共沉淀实验结合免疫印迹分析,证实了中期CL中SF-1与β-连环蛋白之间的相互作用。电泳迁移率变动分析支持SF-1在调节黄体抑制素-α表达中的作用。我们的结果表明,Wnt、cAMP和SF-1在调节黄体抑制素分泌方面可能存在多重相互作用。

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