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Membrane‐Localised Oestrogen Receptor α and β Influence Neuronal Activity Through Activation of Metabotropic Glutamate Receptors
Author(s) -
Mermelstein P. G.
Publication year - 2009
Publication title -
journal of neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.062
H-Index - 116
eISSN - 1365-2826
pISSN - 0953-8194
DOI - 10.1111/j.1365-2826.2009.01838.x
Subject(s) - metabotropic glutamate receptor , intracellular , metabotropic receptor , glutamate receptor , receptor , microbiology and biotechnology , biology , metabotropic glutamate receptor 1 , signal transduction , metabotropic glutamate receptor 7 , neuroscience , biochemistry
Until recently, the idea that oestradiol could affect cellular processes independent of nuclear oestrogen receptors (ERs) was controversial. This was despite the large number of carefully controlled studies performed both within and outside the nervous system demonstrating that oestrogens regulate various intracellular signalling pathways by acting at the membrane surface of cells and/or at biological rates incompatible with the time course of genomic‐initiated events. At present, it is far less controversial that oestradiol acts at surface membrane receptors to regulate nervous system function. Recent studies have demonstrated that the classical intracellular ERs, ERα and ERβ, are major players in mediating the actions of oestradiol on the membrane surface. This review focuses on one potential mechanism by which surface‐localised ERα and ERβ stimulate intracellular signalling events in cells of the nervous system. After oestradiol treatment, both ERα and ERβ are capable of activating different classes of metabotropic glutamate receptors (mGluRs). Oestradiol activation of mGluRs is independent of glutamate, but requires expression of several different caveolin proteins to compartmentalise the different ERs with mGluRs into functional signalling microdomains. ER/mGluR signalling is a potential means by which oestrogens can both rapidly and for extended periods, influence a variety of intracellular signalling processes and behaviours.