Signaling, physiological functions and clinical relevance of the G protein-coupled estrogen receptor GPER

被引:125
|
作者
Prossnitz, Eric R. [1 ,2 ]
Barton, Matthias [3 ]
机构
[1] Univ New Mexico, Dept Cell Biol & Physiol, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Ctr Canc, Albuquerque, NM 87131 USA
[3] Univ Spital Zurich, Dept Innere Med, Klin & Poliklin Innere Med, CH-8091 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Estrogen; Estrogen receptor; GPR30; GPER1; GPER; Cancer; Immune; Vascular; Reproduction; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ENDOTHELIUM-INDEPENDENT RELAXATION; INTIMA-MEDIA THICKNESS; GROWTH-FACTOR RECEPTOR; G-PROTEIN-COUPLED-RECEPTOR-30; GPR30; BREAST-CANCER; GENE-EXPRESSION; UP-REGULATION; IN-VIVO; 17-BETA-ESTRADIOL;
D O I
10.1016/j.prostaglandins.2009.05.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
GPR30, now named GPER1 (G protein-coupled estrogen receptor1) or GPER here, was first identified as an orphan 7-transmembrane G protein-coupled receptor by multiple laboratories using either homology cloning or differential expression and subsequently shown to be required for estrogen-mediated signaling in certain cancer cells. The actions of estrogen are extensive in the body and are thought to be mediated predominantly by classical nuclear estrogen receptors that act as transcription factors/regulators. Nevertheless. certain aspects of estrogen function remain incompatible with the generally accepted mechanisms of classical estrogen receptor action. Many recent studies have revealed that GPER contributes to some of the actions of estrogen, including rapid signaling events and rapid transcriptional activation. With the introduction of GPER-selective ligands and GPER knockout mice, the functions of GPER are becoming more clearly defined. In many cases, there appears to be a complex interplay between the two receptor systems, suggesting that estrogen-mediated physiological responses may be mediated by either receptor or a combination of both receptor types, with important medical implications. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 97
页数:9
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