The overarching goal of this work is to understand the process of sexual differentiation of the brain. Currently, the hormonal control of cell death is the best-established mechanism for creating sex differences in the nervous system. Nonetheless, very little is known about how hormones such as testosterone regulate neuronal cell death. This project will examine the mechanisms underlying hormonally controlled cell death in three well-studied model systems of the brain and spinal cord: the bed nucleus of the stria terminalis (BNST), the anteroventral periventricular nucleus (AVPV) of the hypothalamus, and the spinal nucleus of the bulbocavernosus (SNB). Mice will be used throughout, to take advantage of the power of genetically manipulated strains. Testosterone decreases cell death in the BNST and SNB, and increases it in AVPV. To specify the steps between production of testosterone and the decision of a cell to live or die, and to gain insight into how testosterone exerts opposite effects on cell survival in the different nuclei, the hormone metabolites and receptors that mediate hormonal effects will be identified in Aim 1. It will be determined whether androgenic or estrogenic metabolites of testosterone control sexual differentiation in the three model systems, and receptor subtype-specific agonists will be used to zero in on the specific receptors involved. The pro-apoptotic protein, Bax is required for cell death in the BNSTp, AVPV, and SNB.
In Aim 2 the subcellular localization of Bax, and the expression of proteins that interact with Bax will be examined in control and testosterone-treated animals. Because testosterone pushes cell death in opposite directions in the BNST and AVPV, it is predicted that hormone treatments will differentially affect death-regulatory proteins in these neural areas. Finally, Aim 3 will test the hypothesis that chromatin remodeling is required for sexual differentiation of the brain. This hypothesis will be tested by examining the effect on sexual differentiation of disrupting histone deacetylation during a critical perinatal period and by identifying hormone-dependent changes in histones associated with the cell death genes shown to be important in Aim 2. Together, these studies will determine at a mechanistic level how hormones control sexual differentiation of the nervous system. This work is relevant to understanding sex differences in susceptibility to human neurodevelopmental disorders, and psychiatric and neurodegenerative diseases in adulthood.

Public Health Relevance

Many neurological and psychiatric disorders exhibit sex differences in incidence, severity, or response to treatment. Differences in brain development in males and females likely explain some of these gender differences. This work explores the mechanisms responsible for the development of sex differences in the brain, including a brain region important for sex differences in anxiety and the response to stress.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH068482-10
Application #
8464267
Study Section
Neuroendocrinology, Neuroimmunology, and Behavior Study Section (NNB)
Program Officer
Panchision, David M
Project Start
2003-07-01
Project End
2014-04-30
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
10
Fiscal Year
2013
Total Cost
$245,023
Indirect Cost
$77,487
Name
Georgia State University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
837322494
City
Atlanta
State
GA
Country
United States
Zip Code
30302
Shen, Erica Y; Ahern, Todd H; Cheung, Iris et al. (2015) Epigenetics and sex differences in the brain: A genome-wide comparison of histone-3 lysine-4 trimethylation (H3K4me3) in male and female mice. Exp Neurol 268:21-9
Ahern, Todd H; Krug, Stefanie; Carr, Audrey V et al. (2013) Cell death atlas of the postnatal mouse ventral forebrain and hypothalamus: effects of age and sex. J Comp Neurol 521:2551-69
Gilmore, Richard F; Varnum, Megan M; Forger, Nancy G (2012) Effects of blocking developmental cell death on sexually dimorphic calbindin cell groups in the preoptic area and bed nucleus of the stria terminalis. Biol Sex Differ 3:5
Holmes, Melissa M; Niel, Lee; Anyan, Jeff J et al. (2011) Effects of Bax gene deletion on social behaviors and neural response to olfactory cues in mice. Eur J Neurosci 34:1492-9
Murray, E K; Varnum, M M; Fernandez, J L et al. (2011) Effects of neonatal treatment with valproic acid on vasopressin immunoreactivity and olfactory behaviour in mice. J Neuroendocrinol 23:906-14
Semaan, Sheila J; Murray, Elaine K; Poling, Matthew C et al. (2010) BAX-dependent and BAX-independent regulation of Kiss1 neuron development in mice. Endocrinology 151:5807-17
Hisasue, Shin-ichi; Seney, Marianne L; Immerman, Eleanor et al. (2010) Control of cell number in the bed nucleus of the stria terminalis of mice: role of testosterone metabolites and estrogen receptor subtypes. J Sex Med 7:1401-9
Forger, Nancy G; de Vries, Geert J (2010) Cell death and sexual differentiation of behavior: worms, flies, and mammals. Curr Opin Neurobiol 20:776-83
McCarthy, Margaret M; Auger, Anthony P; Bale, Tracy L et al. (2009) The epigenetics of sex differences in the brain. J Neurosci 29:12815-23
Holmes, M M; McCutcheon, J; Forger, N G (2009) Sex differences in NeuN- and androgen receptor-positive cells in the bed nucleus of the stria terminalis are due to Bax-dependent cell death. Neuroscience 158:1251-6

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