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促卵泡激素通过支持细胞增殖和非经典的环磷酸腺苷介导的抗苗勒管激素(AMH)基因激活来增加睾丸抗苗勒管激素的产生。

Follicle-stimulating hormone increases testicular Anti-Mullerian hormone (AMH) production through sertoli cell proliferation and a nonclassical cyclic adenosine 5'-monophosphate-mediated activation of the AMH Gene.

作者信息

Lukas-Croisier Céline, Lasala Celina, Nicaud Juliette, Bedecarrás Patricia, Kumar T Rajendra, Dutertre Martin, Matzuk Martin M, Picard Jean-Yves, Josso Nathalie, Rey Rodolfo

机构信息

Centro de Investigaciones Endocrinológicas, Hospital de Niños, Gallo 1330, C1425EFD Buenos Aires, Argentina.

出版信息

Mol Endocrinol. 2003 Apr;17(4):550-61. doi: 10.1210/me.2002-0186. Epub 2003 Jan 2.

Abstract

Anti-Müllerian hormone (AMH) production by testicular Sertoli cells is high before puberty and can be further induced by FSH. Our objective was to delineate the mechanisms by which FSH stimulates AMH production. Assay of serum AMH levels and histological morphometric analysis in prepubertal FSH-deficient transgenic mice showed that serum AMH and testicular mass were decreased owing to reduced Sertoli cell number. All parameters resumed normal values in mice treated with recombinant FSH. We also analyzed the ability of FSH and the factors involved in its signaling pathway to activate AMH transcription by transfecting AMH promoter-luc reporter constructs of different lengths in a prepubertal Sertoli cell line. Our results showed that FSH activates AMH transcription via adenylate cyclase, cAMP, and protein kinase A but involving a nonclassical cAMP-response pathway requiring nuclear factor-kappaB and activating protein 2 binding sites, which lie more than 1.9 kb upstream of the AMH transcription start site. This is the first report showing the importance of distant sequences in the regulation of AMH expression. We conclude that prepubertal testicular AMH production is increased by FSH stimulation through Sertoli cell proliferation and an enhancement of AMH gene transcription.

摘要

青春期前睾丸支持细胞产生抗苗勒管激素(AMH)的水平很高,且可被促卵泡激素(FSH)进一步诱导。我们的目的是阐明FSH刺激AMH产生的机制。对青春期前FSH缺陷型转基因小鼠的血清AMH水平进行检测及组织学形态计量分析,结果显示,由于支持细胞数量减少,血清AMH水平和睾丸质量均下降。用重组FSH治疗的小鼠所有参数均恢复正常。我们还通过在青春期前支持细胞系中转染不同长度的AMH启动子-荧光素酶报告基因构建体,分析了FSH及其信号通路中相关因子激活AMH转录的能力。我们的结果表明,FSH通过腺苷酸环化酶、cAMP和蛋白激酶A激活AMH转录,但涉及一条非经典的cAMP反应途径,该途径需要核因子-κB和激活蛋白2结合位点,这些位点位于AMH转录起始位点上游超过1.9 kb处。这是首次报道显示远端序列在AMH表达调控中的重要性。我们得出结论,青春期前FSH通过支持细胞增殖和增强AMH基因转录刺激睾丸AMH产生。

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