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PMID: 20506473 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Cellular and subcellular localization of estrogen and progestin receptor immunoreactivities in the mouse hippocampus.

The Journal of comparative neurology ·Vol. 518 ·No. 14 ·2010-07-15 ·Pages 2729-43

Mitterling KL, Spencer JL, Dziedzic N, Shenoy S, McCarthy K, Waters EM, McEwen BS, Milner TA

Abstract

Estrogen receptor-alpha (ERalpha), estrogen receptor-beta (ERbeta), and progestin receptor (PR) immunoreactivities are localized to extranuclear sites in the rat hippocampal formation. Because rats and mice respond differently to estradiol treatment at a cellular level, the present study examined the distribution of ovarian hormone receptors in the dorsal hippocampal formation of mice. For this, antibodies to ERalpha, ERbeta, and PR were localized by light and electron immunomicroscopy in male and female mice across the estrous cycle. Light microscopic examination of the mouse hippocampal formation showed sparse nuclear ERalpha and PR immunoreactivity (-ir) most prominently in the CA1 region and diffuse ERbeta-ir primarily in the CA1 pyramidal cell layer as well as in a few interneurons. Ultrastructural analysis additionally revealed discrete extranuclear ERalpha-, ERbeta-, and PR-ir in neuronal and glial profiles throughout the hippocampal formation. Although extranuclear profiles were detected in all animal groups examined, the amount and types of profiles varied with sex and estrous cycle phase. ERalpha-ir was highest in diestrus females, particularly in dendritic spines, axons, and glia. Similarly, ERbeta-ir was highest in estrus and diestrus females, mainly in dendritic spines and glia. Conversely, PR-ir was highest during proestrus, mostly in axons. Except for very low levels of extranuclear ERbeta-ir in mossy fiber terminals in mice, the labeling patterns in the mice for all three antibodies were similar to the ultrastructural labeling found previously in rats, suggesting that regulation of these receptors is well conserved across the two species.

MeSH Terms
Animals CA1 Region, Hippocampal/metabolism Estrogen Receptor alpha/metabolism Estrogen Receptor beta/metabolism Estrous Cycle/physiology Female Hippocampus/metabolism,ultrastructure Interneurons/metabolism,ultrastructure Intracellular Space/metabolism Male Mice Mice, Inbred C57BL Neuroglia/metabolism,ultrastructure Neurons/metabolism Pyramidal Cells/metabolism,ultrastructure Receptors, Progesterone/metabolism Sex Characteristics
Chemicals
Estrogen Receptor alpha Estrogen Receptor beta Receptors, Progesterone
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Mitterling Katherine L
Harold and Margaret Milliken Hatch Laboratory of Neuroendocrinology, The Rockefeller University, New York, New York 10065, USA.
Spencer Joanna L
Dziedzic Noelle
Shenoy Sushila
McCarthy Katharine
Waters Elizabeth M
McEwen Bruce S
Milner Teresa A
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Article Info
Journal
The Journal of comparative neurology
Abbr.
J Comp Neurol
ISSN
1096-9861
Published
2010-07-15
Pages
2729-43
Language
English
Region
United States
NLM ID
0406041
PMCID
PMC2879091
Subset
IM
Grants
NINDS NIH HHS · R01 NS007080 · United States
NIGMS NIH HHS · GM07739 · United States
NIDA NIH HHS · R01 DA008259 · United States
NIMH NIH HHS · F30 MH082528 · United States
NINDS NIH HHS · R01 NS007080-41 · United States
NIGMS NIH HHS · T32 GM007739 · United States
NIMH NIH HHS · F30 MH082528-01 · United States
NIDA NIH HHS · R01 DA008259-15 · United States
NIDA NIH HHS · DA08259 · United States
NHLBI NIH HHS · HL18974 · United States
NIDDK NIH HHS · T32 DK07313 · United States
NINDS NIH HHS · NS007080 · United States
NIDDK NIH HHS · T32 DK007313-23 · United States
NINDS NIH HHS · R01 NS007080-42 · United States
NHLBI NIH HHS · P01 HL018974 · United States
NIDDK NIH HHS · T32 DK007313 · United States
NIDA NIH HHS · R01 DA008259-16 · United States
NHLBI NIH HHS · P01 HL018974-309002 · United States
NINDS NIH HHS · R01 NS007080-43 · United States
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