Estrogen signaling through the transmembrane G protein-coupled receptor GrPR30

被引:493
|
作者
Prossnitz, Eric R. [1 ,2 ]
Arterburn, Jeffrey B. [2 ,3 ]
Smith, Harriet O. [2 ,4 ]
Oprea, Tudor I. [2 ,5 ]
Sklar, Larry A. [2 ,6 ]
Hathaway, Helen J. [1 ,2 ]
机构
[1] Dept Cell Biol & Physiol, Mexico City, DF, Mexico
[2] Univ New Mexico, Ctr Canc, Albuquerque, NM 87131 USA
[3] New Mexico State Univ, Dept Chem & Biochem, Las Cruces, NM 88003 USA
[4] Dept Obstet & Gynecol, Mexico City, DF, Mexico
[5] Div Biocomp, Mexico City, DF, Mexico
[6] Univ New Mexico, Dept Pathol, Ctr Hlth Sci, Albuquerque, NM 87131 USA
关键词
estrogen receptor; steroid receptor; epidermal growth factor receptor;
D O I
10.1146/annurev.physiol.70.113006.100518
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Steroids play an important role in the regulation of normal physiology and the treatment of disease. Steroid receptors have classically been described as ligand-activated transcription factors mediating long-term genomic effects in hormonally regulated tissues. It is now clear that steroids also mediate rapid signaling events traditionally associated with growth factor receptors and G protein-coupled receptors. Although evidence suggests that the classical steroid receptors are capable of mediating many of these events, more recent discoveries reveal the existence of transmembrane receptors capable of responding to steroids with cellular activation. One such receptor, GPR30, is a member of the G protein-coupled receptor superfamily and mediates estrogen-dependent kinase activation as well as transcriptional responses. In this review, we provide an overview of the evidence for the cellular and physiological actions of GPR30 in estrogen-dependent processes and discuss the relationship of GPR30 with classical estrogen receptors.
引用
收藏
页码:165 / 190
页数:26
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