Affiliation:
1. Division of Endocrinology, Veterans Affairs Medical Center, Long Beach, Long Beach 90822; and Departments of Medicine and Pharmacology, University of California, Irvine, Irvine, California 92717
Abstract
The existence of binding proteins for the female sex steroid, 17β-estradiol, has been known for almost 50 years. Presently, two estrogen receptors (ERs), ER-α and ER-β, have been cloned in mammals, and they are expressed in many cell types of metazoans. ERs act primarily as nuclear transcription factors, and this effect is enhanced by ligand binding. Emerging data have identified a separate pool of receptors for this steroid in the plasma membrane, but the mechanisms of action and cellular functions of these proteins are just beginning to be defined. In this review, the known details of the nuclear and plasma membrane ER functions will be discussed. A particular focus will be to define the signaling pathways from the membrane that lead to important cell physiology effects of estrogen. The potential interactions of membrane ER with other local proteins will also be discussed, and the unique but often complementary roles of the receptor pools will be highlighted. These details may be of additional relevance to other steroid receptors, since there is evidence of their existence in the cell membrane.
Publisher
American Physiological Society
Subject
Physiology (medical),Physiology
Cited by
244 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献