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      Stable Density and Dynamics of Dendritic Spines of Cortical Neurons Across the Estrous Cycle While Expressing Differential Levels of Sensory-Evoked Plasticity

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          Abstract

          Periodic oscillations of gonadal hormone levels during the estrous cycle exert effects on the female brain, impacting cognition and behavior. While previous research suggests that changes in hormone levels across the cycle affect dendritic spine dynamics in the hippocampus, little is known about the effects on cortical dendritic spines and previous studies showed contradictory results. In this in vivo imaging study, we investigated the impact of the estrous cycle on the density and dynamics of dendritic spines of pyramidal neurons in the primary somatosensory cortex of mice. We also examined if the induction of synaptic plasticity during proestrus, estrus, and metestrus/diestrus had differential effects on the degree of remodeling of synapses in this brain area. We used chronic two-photon excitation (2PE) microscopy during steady-state conditions and after evoking synaptic plasticity by whisker stimulation at the different stages of the cycle. We imaged apical dendritic tufts of layer 5 pyramidal neurons of naturally cycling virgin young female mice. Spine density, turnover rate (TOR), survival fraction, morphology, and volume of mushroom spines remained unaltered across the estrous cycle, and the values of these parameters were comparable with those of young male mice. However, while whisker stimulation of female mice during proestrus and estrus resulted in increases in the TOR of spines (74.2 ± 14.9% and 75.1 ± 12.7% vs. baseline, respectively), sensory-evoked plasticity was significantly lower during metestrus/diestrus (32.3 ± 12.8%). In males, whisker stimulation produced 46.5 ± 20% increase in TOR compared with baseline—not significantly different from female mice at any stage of the cycle. These results indicate that, while steady-state density and dynamics of dendritic spines of layer 5 pyramidal neurons in the primary somatosensory cortex of female mice are constant during the estrous cycle, the susceptibility of these neurons to sensory-evoked structural plasticity may be dependent on the stage of the cycle. Since dendritic spines are more plastic during proestrus and estrus than during metestrus/diestrus, certain stages of the cycle could be more suitable for forms of memory requiring de novo formation and elimination of spines and other stages for forms of memory where retention and/or repurposing of already existing synaptic connections is more pertinent.

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          Most cited references36

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          Assessing reproductive status/stages in mice.

          The short reproductive cycle length observed in rodents, called the estrous cycle, makes them an ideal animal model for investigation of changes that occur during the reproductive cycle. Most of the data in the literature about the estrous cycle is obtained from rats because they are easily manipulated and they exhibit a clear and well-defined estrous cycle. However, the increased number of experiments using knockout mice requires identification of their estrous cycle as well, since (in)fertility issues may arise. In mice, like rats, the identification of the stage of estrous cycle is based on the proportion of cell types observed in the vaginal secretion. The aim of this unit is to provide guidelines for quickly and accurately determining estrous cycle phases in mice. Copyright 2009 by John Wiley & Sons, Inc.
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            Experience leaves a lasting structural trace in cortical circuits

            Sensory experiences exert a powerful influence on the function and future performance of neuronal circuits in the mammalian neocortex1-3. Restructuring of synaptic connections is believed to be one mechanism by which cortical circuits store information about the sensory world4,5. Excitatory synaptic structures, such as dendritic spines, are dynamic entities6-8 which remain sensitive to alteration of sensory input throughout life6,9. It remains unclear, however, whether structural changes at the level of dendritic spines can outlast the original experience and thereby provide a morphological basis for long-term information storage. Here we follow spine dynamics on apical dendrites of pyramidal neurons in functionally-defined regions of adult mouse visual cortex during plasticity of eye-specific responses induced by repeated closure of one eye (monocular deprivation, MD). The first MD episode doubled the rate of spine formation, thereby increasing spine density. This effect was specific to layer 5 cells located in binocular cortex where most neurons increase their responsiveness to the non-deprived eye3,10. Restoring binocular vision returned spine dynamics to baseline levels, but absolute spine density remained elevated and many MD-induced spines persisted during this period of functional recovery. Remarkably, spine addition did not increase again when the same eye was closed for the second time. This absence of structural plasticity stands out against the robust changes of eye specific responses which occur even faster upon repeated deprivation3. Thus, spines added during the first MD experience might provide a structural basis for subsequent functional shifts. These results provide a strong link between functional plasticity and specific synaptic rearrangements, revealing a mechanism of how prior experiences could be stored in cortical circuits.
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              Immunolocalization of estrogen receptor beta in the mouse brain: comparison with estrogen receptor alpha.

              Estrogen receptor alpha (ER alpha) and ER beta are members of the steroid nuclear receptor family that modulate gene transcription in an estrogen-dependent manner. ER mRNA and protein have been detected both peripherally and in the central nervous system, with most data having come from the rat. Here we report the development of an ER beta-selective antibody that cross-reacts with mouse, rat, and human ER beta protein and its use to determine the distribution of ER beta in the murine brain. Further, a previously characterized polyclonal antibody to ER alpha was used to compare the distribution of the two receptors in the first comprehensive description of ER distribution specifically in the mouse brain. ER beta immunoreactivity (ir) was primarily localized to cell nuclei within select regions of the brain, including the olfactory bulb, cerebral cortex, septum, preoptic area, bed nucleus of the stria terminalis, amygdala, paraventricular hypothalamic nucleus, thalamus, ventral tegmental area, substantia nigra, dorsal raphe, locus coeruleus, and cerebellum. Extranuclear-ir was detected in several areas, including fibers of the olfactory bulb, CA3 stratum lucidum, and CA1 stratum radiatum of the hippocampus and cerebellum. Although both receptors were generally expressed in a similar distribution through the brain, nuclear ER alpha-ir was the predominant subtype in the hippocampus, preoptic area, and most of the hypothalamus, whereas it was sparse or absent from the cerebral cortex and cerebellum. Collectively, these findings demonstrate the region-selective expression of ER beta and ER alpha in the adult ovariectomized mouse brain. These data provide an anatomical framework for understanding the mechanisms by which estrogen regulates specific neural systems in the mouse.
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                Author and article information

                Contributors
                Journal
                Front Mol Neurosci
                Front Mol Neurosci
                Front. Mol. Neurosci.
                Frontiers in Molecular Neuroscience
                Frontiers Media S.A.
                1662-5099
                16 March 2018
                2018
                : 11
                : 83
                Affiliations
                [1] 1Department of Pharmacology, Tulane University School of Medicine, Tulane University , New Orleans, LA, United States
                [2] 2Neuroscience Program, Brain Institute, Tulane University , New Orleans, LA, United States
                [3] 3Department of Cell and Molecular Biology, Tulane University , New Orleans, LA, United States
                [4] 4Brain Institute, Tulane University , New Orleans, LA, United States
                Author notes

                Edited by: Jordan Marrocco, Rockefeller University, United States

                Reviewed by: Deepak Prakash Srivastava, King’s College London, United Kingdom; Pirta Elina Hotulainen, Minerva Institute for Medical Research, Finland; Volker Scheuss, Max Planck Institute of Neurobiology (MPG), Germany

                *Correspondence: Ricardo Mostany rmostany@ 123456tulane.edu
                Article
                10.3389/fnmol.2018.00083
                5864847
                29615867
                370fbacb-5662-4a3d-bc18-2bdc3551e028
                Copyright © 2018 Alexander, Barnes, Trimmer, Davidson, Ogola, Lindsey and Mostany.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 November 2017
                : 01 March 2018
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 51, Pages: 13, Words: 10050
                Funding
                Funded by: National Institute on Aging 10.13039/100000049
                Award ID: R01AG047296
                Funded by: Louisiana Board of Regents 10.13039/100006952
                Award ID: LEQSF(2016-19)-RD-A-24, LEQSF-EPS(2015)-PFUND-416
                Funded by: National Institute of General Medical Sciences 10.13039/100000057
                Award ID: 5P20GM103629
                Categories
                Neuroscience
                Original Research

                Neurosciences
                synaptic plasticity,estrous cycle,two-photon imaging,pyramidal neurons,female,estrogens,dendritic spines

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