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      Estradiol Increases Microglial Response to Lipopolysaccharide in the Ventromedial Hypothalamus during the Peripubertal Sensitive Period in Female Mice

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          Abstract

          Sensitive periods are times of development during which the effects of experience are unusually strong and long lasting. The peripubertal period has emerged as one such sensitive period, and a single administration of lipopolysaccharide (LPS) during this time reduces hormone-induced sexual behavior in adult female mice. During periods of high synaptic turnover, maturation, and elimination, as occurs during this sensitive period, microglia are particularly active. Estradiol also regulates microglial numbers, morphology, and activation. In addition, a good deal of evidence suggests that estradiol may confer this vulnerability to the effects of a stressor during the peripubertal period. Therefore, we investigated the effects of estradiol on microglial morphology, cytokine levels, and the sickness response to LPS. Estradiol levels were manipulated by implanting an estradiol-filled SILASTIC capsule (or oil-filled control) in ovariectomized mice or by administering the aromatase inhibitor, formestane (or oil control), to ovary-intact mice. We found that (1) estradiol elevates basal microglial Iba1 immunoreactivity in the ventromedial nucleus of the hypothalamus (VMH), (2) LPS induces higher levels of proinflammatory cytokines in the presence of estradiol, and (3) LPS causes hypothermia in the presence of estradiol. Taken together, these data suggest that estradiol enhances the effect of LPS during the pubertal sensitive period.

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          Most cited references34

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          The immune system and developmental programming of brain and behavior.

          The brain, endocrine, and immune systems are inextricably linked. Immune molecules have a powerful impact on neuroendocrine function, including hormone-behavior interactions, during health as well as sickness. Similarly, alterations in hormones, such as during stress, can powerfully impact immune function or reactivity. These functional shifts are evolved, adaptive responses that organize changes in behavior and mobilize immune resources, but can also lead to pathology or exacerbate disease if prolonged or exaggerated. The developing brain in particular is exquisitely sensitive to both endogenous and exogenous signals, and increasing evidence suggests the immune system has a critical role in brain development and associated behavioral outcomes for the life of the individual. Indeed, there are associations between many neuropsychiatric disorders and immune dysfunction, with a distinct etiology in neurodevelopment. The goal of this review is to describe the important role of the immune system during brain development, and to discuss some of the many ways in which immune activation during early brain development can affect the later-life outcomes of neural function, immune function, mood and cognition. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Microglia are essential to masculinization of brain and behavior.

            Brain sexual differentiation in rodents results from the perinatal testicular androgen surge. In the preoptic area (POA), estradiol aromatized from testosterone upregulates the production of the proinflammatory molecule, prostaglandin E(2) (PGE(2)) to produce sex-specific brain development. PGE(2) produces a two-fold greater density of dendritic spines in males than in females and masculinizes adult copulatory behavior. One neonatal dose of PGE(2) masculinizes the POA and behavior, and simultaneous treatment with an inhibitor of additional prostaglandin synthesis prevents this masculinization, indicating a positive feedforward process that leads to sustained increases in PGE(2). The mechanisms underlying this feedforward process were unknown. Microglia, the primary immunocompetent cells in the brain, are active neonatally, contribute to normal brain development, and both produce and respond to prostaglandins. We investigated whether there are sex differences in microglia in the POA and whether they influence developmental masculinization. Neonatal males had twice as many ameboid microglia as females and a more activated morphological profile, and both estradiol and PGE(2) masculinized microglial number and morphology in females. Microglial inhibition during the critical period for sexual differentiation prevented sex differences in microglia, estradiol-induced masculinization of dendritic spine density, and adult copulatory behavior. Microglial inhibition also prevented the estradiol-induced upregulation of PGE(2), indicating that microglia are essential to the feedforward process through which estradiol upregulates prostaglandin production. These studies demonstrate that immune cells in the brain interact with the nervous and endocrine systems during development, and are crucial for sexual differentiation of brain and behavior.
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              Cytokine-induced sickness behavior: mechanisms and implications.

              Sickness behavior refers to a coordinated set of behavioral changes that develop in sick individuals during the course of an infection. At the molecular level, these changes are due to the brain effects of proinflammatory cytokines such as interleukin-1 (IL-1) and tumor necrosis factor alpha (TNFalpha). Peripherally released cytokines act on the brain via a fast transmission pathway involving primary afferent nerves innervating the bodily site of inflammation and a slow transmission pathway involving cytokines originating from the choroid plexus and circumventricular organs and diffusing into the brain parenchyma by volume transmission. At the behavioral level, sickness behavior appears to be the expression of a central motivational state that reorganizes the organism priorities to cope with infectious pathogens. There is evidence that the sickness motivational state can interact with other motivational states and respond to nonimmune stimuli probably by way of sensitization and/or classical conditioning. However, the mechanisms that are involved in plasticity of the sickness motivational state are not yet understood.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                18 June 2020
                2 July 2020
                Jul-Aug 2020
                : 7
                : 4
                : ENEURO.0505-19.2020
                Affiliations
                [1 ]Department of Psychological and Brain Sciences, University of Massachusetts , Amherst, MA 01003
                [2 ]Neuroscience and Behavior Program, University of Massachusetts , Amherst, MA 01003
                [3 ]Center for Neuroendocrine Studies, University of Massachusetts , Amherst, MA 01003
                Author notes

                The authors declare no competing financial interests.

                Author contributions: A.V.-P. and J.D.B. designed research; A.V.-P. and S.F. performed research; A.V.-P. and M.K.H. analyzed data; A.V.-P., M.K.H., and J.D.B. wrote the paper.

                This work was supported by the National Science Foundation Grant IOS 1050179 (to J.D.B.).

                M. K. Holder’s present address: School of Psychology, Georgia Institute of Technology, Atlanta, GA 30332.

                Correspondence should be addressed to Mary K. Holder at mary.holder@ 123456psych.gatech.edu .
                Author information
                https://orcid.org/0000-0002-3811-5028
                Article
                eN-NWR-0505-19
                10.1523/ENEURO.0505-19.2020
                7333979
                32554430
                2fa130fd-b0a7-4878-9cf4-14f8003ec023
                Copyright © 2020 Velez-Perez et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 27 November 2019
                : 5 May 2020
                : 9 June 2020
                Page count
                Figures: 7, Tables: 2, Equations: 0, References: 46, Pages: 14, Words: 00
                Funding
                Funded by: http://doi.org/10.13039/100000001National Science Foundation (NSF)
                Award ID: IOS 1050179
                Categories
                5
                Research Article: New Research
                Integrative Systems
                Custom metadata
                July/August 2020

                estradiol,iba1,mice,microglia,peripubertal development
                estradiol, iba1, mice, microglia, peripubertal development

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