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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
The existence of binding proteins for the
female sex steroid, 17
-estradiol, has been known for almost 50 years. Presently, two estrogen receptors (ERs), ER-
and ER-
, 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.
nuclear receptors; apoptosis; membrane receptors; steroid receptors; signal transduction; cell proliferation
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