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G 蛋白偶联受体 48 通过 cAMP/PKA 信号通路在上生殖道上调雌激素受体 α 的表达。

G protein-coupled receptor 48 upregulates estrogen receptor alpha expression via cAMP/PKA signaling in the male reproductive tract.

机构信息

Shanghai Clinical Center for Endocrine and Metabolic Diseases, Shanghai Key Laboratory of Endocrine Tumor, Shanghai Institute of Endocrinology and Metabolism, Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, 197 RuiJin 2nd Road, Shanghai 200025, China.

出版信息

Development. 2010 Jan;137(1):151-7. doi: 10.1242/dev.040659.

Abstract

The epididymis and efferent ducts play major roles in sperm maturation, transport, concentration and storage by reabsorbing water, ions and proteins produced from seminiferous tubules. Gpr48-null male mice demonstrate reproductive tract defects and infertility. In the present study, we found that estrogen receptor alpha (ERalpha) was dramatically reduced in the epididymis and efferent ducts in Gpr48-null male mice. We further revealed that ERalpha could be upregulated by Gpr48 activation via the cAMP/PKA signaling pathway. Moreover, we identified a cAMP responsive element (Cre) motif located at -1307 to -1300 bp in the ERalpha promoter that is able to interact with Cre binding protein (Creb). In conclusion, Gpr48 participates in the development of the male epididymis and efferent ducts through regulation of ERalpha expression via the cAMP/PKA signaling pathway.

摘要

附睾和输出管通过重吸收来自精小管的水、离子和蛋白质,在精子成熟、运输、浓缩和储存中起主要作用。Gpr48 敲除雄性小鼠表现出生殖道缺陷和不育。在本研究中,我们发现 Gpr48 敲除雄性小鼠的附睾和输出管中雌激素受体 alpha (ERalpha) 显著减少。我们进一步揭示,Gpr48 通过 cAMP/PKA 信号通路激活可以上调 ERalpha。此外,我们鉴定出 ERalpha 启动子中位于 -1307 至 -1300bp 的 cAMP 反应元件 (Cre) 基序,该基序能够与 Cre 结合蛋白 (Creb) 相互作用。总之,Gpr48 通过 cAMP/PKA 信号通路调节 ERalpha 的表达,参与雄性附睾和输出管的发育。

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