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ORIGINAL RESEARCH ARTICLE

Novel Localization of NMDA Receptors Within Neuroendocrine Gonadotropin-Releasing Hormone Terminals

Weiling Yin^*,, John M. Mendenhall, Shawn B. Bratton^*,, Twethida Oung, William G. M. Janssen, John H. Morrison and Andrea C. Gore^*,,,,1

^* Division of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin, Austin, Texas 78712; Kastor Neurobiology of Aging Labs, Fishberg Department of Neuroscience, and Brookdale Department of Geriatrics, Mount Sinai School of Medicine, New York, New York 10029; Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas 78712; and Institute for Neuroscience, The University of Texas at Austin, Austin, Texas 78712

To whom requests for reprints should be addressed at ¹ Pharmacology/Toxicology A1915, University of Texas at Austin, Austin, TX 78712. E-mail: andrea.gore{at}mail.utexas.edu

About 1000 hypothalamic neurons synthesize and release gonadotropin-releasing hormone (GnRH), the master molecule of reproduction in all mammals. At the level of the median eminence at the base of the brain, where GnRH and other hypothalamic releasing hormones are secreted into the capillary system leading to the anterior pituitary gland, there is non-synaptic regulation of neurohormone release by a number of central neurotransmitters. For example, glutamate, the major excitatory amino acid in the brain, directly regulates GnRH release from nerve terminals via NMDA receptors (NMDARs). Moreover, the effects of glutamate action on GnRH secretion are potentiated by estrogens, and this relates to the physiologic control of ovulation by the hypothalamus. We sought to determine the ultrastructural relationship between GnRH neuroterminals and NMDARs, and this regulation by estradiol. Using immunofluorescent confocal microscopy, postembedding immunogold electron microscopy, fractionation, and Western blotting, we demonstrated: (i) GnRH is localized in large dense-core vesicles of neurosecretory profiles/terminals, (ii) the NMDAR1 subunit is found primarily on large dense-core vesicles of neurosecretory profiles/terminals, (iii) there is extensive colocalization of GnRH and NMDAR1 on the same vesicles, and (iv) estradiol modestly but significantly alters the distribution of NMDAR1 in GnRH neuroterminals by increasing expression of NMDAR1 on large dense-core vesicles. Western blots of fractionated median eminence support the presence of NMDAR1 in subcellular fractions containing large dense-core vesicles. These data are the first to show the presence of the NMDAR on neuroendocrine secretory vesicles, its co-expression with GnRH, and its regulation by estradiol. The results provide a novel anatomical site for the NMDAR and may represent a new mechanism for the regulation of GnRH release.

Key Words: GnRH • NMDA receptor • estrogen • median eminence • electron microscopy • large dense-core vesicle

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