Department of Pharmaco-Biology, University of Calabria, 87030 Rende, Italy.
J Endocrinol. 2010 Feb;204(2):105-14. doi: 10.1677/JOE-09-0242. Epub 2009 Sep 18.
Steroid hormones such as estrogens are known to signal through ligand-regulated transcription factors of the nuclear receptor superfamily. In addition, they elicit rapid nongenomic responses from membrane-associated receptors. One of these receptors belongs to an entirely different family of proteins. The G protein-coupled and seven-transmembrane receptor, GPR30, is now widely recognized as an estrogen receptor (ER), hence its official new acronym GPER. It appears to mediate a wide range of responses to estrogen in a large variety of cell types. Its functions are clearly distinct from those of the classical nuclear ERs, although these pathways may overlap and interact in some cases. Here, we review the history of the discovery of this new ER, the evidence for the claim that it is an ER, its signal transduction, and its potential functions in physiology and disease.
甾体激素(如雌激素)已知通过核受体超家族的配体调节转录因子进行信号转导。此外,它们还从膜相关受体引发快速的非基因组反应。这些受体之一属于完全不同的蛋白家族。G 蛋白偶联和七跨膜受体 GPR30 现在被广泛认为是一种雌激素受体(ER),因此其官方的新缩写为 GPER。它似乎在多种细胞类型中介导对雌激素的广泛反应。其功能明显不同于经典的核 ER,尽管在某些情况下这些途径可能重叠和相互作用。在这里,我们回顾了这个新 ER 的发现历史、它作为 ER 的证据、它的信号转导以及它在生理学和疾病中的潜在功能。