The research of the Section on Neuroendocrine Immunology and Behavior (SNIB) focuses on (Project 1) molecular basis of differential hypothalamic pituitary adrenal (HPA) axis regulation in inbred rat strains and its relationship to inflammatory disease susceptibility and (Project 2) repression of the glucocorticoid receptor and other nuclear hormone receptors by Bacillus anthracis (anthrax) lethal toxin (LeTx) and its role in inflammatory shock. In Project 1, we have begun to explore the expression within the brain of immune molecules (cytokines and chemokines) in rodents exposed to bacterial cell wall products. Preliminary results indicate that certain immune molecules (chemokines) are expressed within the brain under these conditions. Project 2 focuses on validation and elucidation of the molecular mechanisms and therapeutic implications of our finding that Bacillus anthracis lethal toxin (LeTx) is a potent and selective repressor of nuclear hormone receptors, including the glucocorticoid receptor (GR) and progesterone receptor (PR). These findings have important implications for treatment and prevention of anthrax LeTx and other bacterial toxins? toxicity and lethality. We followed up on initial studies showing that nanomolar concentrations of LeTx selectively repress nuclear hormone receptor activity, including the glucocorticoid receptor (GR), the progesterone receptor (PR) and the estrogen receptor (ER) alpha but not the mineralocorticoid receptor (MR) or ER beta. Since GR antagonists or interruptions of the hypothalamic-pituitary-adrenal (HPA) axis render otherwise shock-resistant animals highly susceptible to the lethal effects of many bacterial products, we postulated that LeTx repression of GR and other nuclear hormone receptors might contribute to anthrax toxicity and lethality. In subsequent studies we have shown that interruption of the HPA axis by adrenalectomy is associated with enhanced LeTx mortality in otherwise LeTx resistant mouse strains. Furthermore, treatment of mice with glucorticoids was associated with enhanced mortality. Follow-up molecular studies show selective repression of nuclear hormone receptors that is partially receptor and partially promoter dependent. Chromatin immunoprecipitation (ChIP) experiments indicate that LeTx inhibits GR binding to the promoter, resulting in loss of both polymerase II binding and acetylation of histone H3 in target genes. Electrophoretic mobility shift assays (EMSA) indicate that this inhibition is not due to direct interaction of LF ? PA with the GR-GRE complex. Taken together, these findings indicate that LeTx represses GR activity through its effects on co-factor(s), or modification of the receptor. These findings together with the in vivo studies indicate that an intact HPA axis (neuroendocrine response) is required for resistance to anthrax lethal toxin, and that simple glucocorticoid replacement may not be sufficient and might be detrimental as a therapy for anthrax LeTx shock.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Intramural Research (Z01)
Project #
1Z01MH002585-15
Application #
7136243
Study Section
(DIRP)
Project Start
Project End
Budget Start
Budget End
Support Year
15
Fiscal Year
2005
Total Cost
Indirect Cost
Name
U.S. National Institute of Mental Health
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Thayer, Julian F; Verkuil, Bart; Brosschot, Jos F et al. (2010) Effects of the physical work environment on physiological measures of stress. Eur J Cardiovasc Prev Rehabil 17:431-9
Butts, Cherie L; Bowers, Eve; Horn, J Cash et al. (2008) Inhibitory effects of progesterone differ in dendritic cells from female and male rodents. Gend Med 5:434-47
Butts, Cherie L; Shukair, Shetha A; Duncan, Kristina M et al. (2007) Evaluation of steroid hormone receptor protein expression in intact cells using flow cytometry. Nucl Recept Signal 5:e007
Tait, A Sasha; Dalton, Monique; Geny, Blandine et al. (2007) The large clostridial toxins from Clostridium sordellii and C. difficile repress glucocorticoid receptor activity. Infect Immun 75:3935-40
Eskandari, Farideh; Martinez, Pedro E; Torvik, Sara et al. (2007) Low bone mass in premenopausal women with depression. Arch Intern Med 167:2329-36
Marques, Andrea H; Cizza, Giovanni; Sternberg, Esther (2007) [Brain-immune interactions and implications in psychiatric disorders] Rev Bras Psiquiatr 29 Suppl 1:S27-32
Sternberg, Esther M; Silverman, Marni N; Cizza, Giovanni (2007) The neuroendocrine system and rheumatoid arthritis: insights from anti-tumor necrosis factor-alpha therapy. J Rheumatol 34:1443-5
Butts, C L; Shukair, S A; Duncan, K M et al. (2007) Effects of dexamethasone on rat dendritic cell function. Horm Metab Res 39:404-12
Butts, Cherie L; Shukair, Shetha A; Duncan, Kristina M et al. (2007) Progesterone inhibits mature rat dendritic cells in a receptor-mediated fashion. Int Immunol 19:287-96
Sternberg, Esther M; Wilson, Matthew A (2006) Neuroscience and architecture: seeking common ground. Cell 127:239-42

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