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高通过 ERK 信号通路增强雌激素受体 α 的活性。

Gαo potentiates estrogen receptor α activity via the ERK signaling pathway.

机构信息

Section of Hematology and Medical Oncology, Department of Medicine, Tulane University, 1430 Tulane Avenue, SL-78, New Orleans, Louisiana 70112, USA.

出版信息

J Endocrinol. 2012 Jul;214(1):45-54. doi: 10.1530/JOE-12-0097. Epub 2012 May 4.

Abstract

The estrogen receptor α (ERα) is a transcription factor that mediates the biological effects of 17β-estradiol (E(2)). ERα transcriptional activity is also regulated by cytoplasmic signaling cascades. Here, several Gα protein subunits were tested for their ability to regulate ERα activity. Reporter assays revealed that overexpression of a constitutively active Gα(o) protein subunit potentiated ERα activity in the absence and presence of E(2). Transient transfection of the human breast cancer cell line MCF-7 showed that Gα(o) augments the transcription of several ERα-regulated genes. Western blots of HEK293T cells transfected with ER±Gα(o) revealed that Gα(o) stimulated phosphorylation of ERK 1/2 and subsequently increased the phosphorylation of ERα on serine 118. In summary, our results show that Gα(o), through activation of the MAPK pathway, plays a role in the regulation of ERα activity.

摘要

雌激素受体 α(ERα)是一种转录因子,介导 17β-雌二醇(E(2))的生物学效应。ERα 的转录活性也受到细胞质信号级联的调节。在这里,测试了几种 Gα 蛋白亚基调节 ERα 活性的能力。报告基因分析显示,组成型激活的 Gα(o)蛋白亚基的过表达增强了 E(2)存在和不存在时 ERα 的活性。瞬时转染人乳腺癌细胞系 MCF-7 表明,Gα(o) 增强了几种 ERα 调节基因的转录。用 ER±Gα(o) 转染的 HEK293T 细胞的 Western blot 显示,Gα(o) 刺激 ERK 1/2 的磷酸化,随后增加 ERα 丝氨酸 118 的磷酸化。总之,我们的结果表明,Gα(o) 通过激活 MAPK 途径,在调节 ERα 活性中发挥作用。

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