The Aryl Hydrocarbon Receptor Is Required for Optimal Resistance to <i>Listeria monocytogenes</i> Infection in Mice
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Denison, M. S., S. Heath-Pagliuso. 1998. The Ah receptor: a regulator of the biochemical and toxicological actions of structurally diverse chemicals. Bull. Environ. Contam. Toxicol. 61: 557-568.
Marlowe, J. L., A. Puga. 2005. Aryl hydrocarbon receptor, cell cycle regulation, toxicity, and tumorigenesis. J. Cell. Biochem. 96: 1174-1184.
Schmidt, J. V., G. H. Su, J. K. Reddy, M. C. Simon, C. A. Bradfield. 1996. Characterization of a murine Ahr null allele: involvement of the Ah receptor in hepatic growth and development. Proc. Natl. Acad. Sci. USA 93: 6731-6736.
Denison, M. S., A. Pandini, S. R. Nagy, E. P. Baldwin, L. Bonati. 2002. Ligand binding and activation of the Ah receptor. Chem. Biol. Interact. 141: 3-24.
Gu, Y. Z., J. B. Hogenesch, C. A. Bradfield. 2000. The PAS superfamily: sensors of environmental and developmental signals. Annu. Rev. Pharmacol. Toxicol. 40: 519-561.
Taylor, B. L., I. B. Zhulin. 1999. PAS domains: internal sensors of oxygen, redox potential, and light. Microbiol. Mol. Biol. Rev. 63: 479-506.
Chen, H. S., G. H. Perdew. 1994. Subunit composition of the heteromeric cytosolic aryl hydrocarbon receptor complex. J. Biol. Chem. 269: 27554-27558.
Meyer, B. K., M. G. Pray-Grant, J. P. Vanden Heuvel, G. H. Perdew. 1998. Hepatitis B virus X-associated protein 2 is a subunit of the unliganded aryl hydrocarbon receptor core complex and exhibits transcriptional enhancer activity. Mol. Cell. Biol. 18: 978-988.
Enan, E., F. Matsumura. 1996. Identification of c-Src as the integral component of the cytosolic Ah receptor complex, transducing the signal of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) through the protein phosphorylation pathway. Biochem. Pharmacol. 52: 1599-1612.
Hankinson, O.. 1995. The aryl hydrocarbon receptor complex. Annu. Rev. Pharmacol. Toxicol. 35: 307-340.
Singh, N. P., M. Nagarkatti, P. S. Nagarkatti. 2007. Role of dioxin response element and nuclear factor-κB motifs in 2,3,7,8-tetrachlorodibenzo-p-dioxin-mediated regulation of Fas and Fas ligand expression. Mol. Pharmacol. 71: 145-157.
Fan, F., B. Yan, G. Wood, M. Viluksela, K. K. Rozman. 1997. Cytokines (IL-1β and TNFα) in relation to biochemical and immunological effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in rats. Toxicology 116: 9-16.
Jensen, B. A., R. J. Leeman, J. J. Schlezinger, D. H. Sherr. 2003. Aryl hydrocarbon receptor (AhR) agonists suppress interleukin-6 expression by bone marrow stromal cells: an immunotoxicology study. Environ. Health 2: 16-28.
N′Diaye, M., E. Le Ferrec, D. Lagadic-Gossmann, S. Corre, D. Gilot, V. Lecureur, P. Monteiro, C. Rauch, M. D. Galibert, O. Fardel. 2006. Aryl hydrocarbon receptor- and calcium-dependent induction of the chemokine CCL1 by the environmental contaminant benzoapyrene. J. Biol. Chem. 281: 19906-19915.
Vogel, C. F., E. Sciullo, P. Wong, P. Kuzmicky, N. Kado, F. Matsumura. 2005. Induction of proinflammatory cytokines and C-reactive protein in human macrophage cell line U937 exposed to air pollution particulates. Environ. Health Perspect. 113: 1536-1541.
Warren, T. K., K. A. Mitchell, B. P. Lawrence. 2000. Exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) suppresses the humoral and cell-mediated immune responses to influenza A virus without affecting cytolytic activity in the lung. Toxicol. Sci. 56: 114-123.
Hinsdill, R. D., D. L. Couch, R. S. Speirs. 1980. Immunosuppression in mice induced by dioxin (TCDD) in feed. J. Environ. Pathol. Toxicol. 4: 401-425.
Luster, M. I., G. A. Boorman, J. H. Dean, M. W. Harris, R. W. Luebke, M. L. Padarathsingh, J. A. Moore. 1980. Examination of bone marrow, immunologic parameters and host susceptibility following pre- and postnatal exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Int. J. Immunopharmacol. 2: 301-310.
Ward, E. C., M. J. Murray, L. D. Lauer, R. V. House, R. Irons, J. H. Dean. 1984. Immunosuppression following 7,12-dimethylbenzanthracene exposure in B6C3F1 mice, I: effects on humoral immunity and host resistance. Toxicol. Appl. Pharmacol. 75: 299-308.
House, R. V., L. D. Lauer, M. J. Murray, P. T. Thomas, J. P. Ehrlich, G. R. Burleson, J. H. Dean. 1990. Examination of immune parameters and host resistance mechanisms in B6C3F1 mice following adult exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin. J. Toxicol. Environ. Health 31: 203-215.
Kerkvliet, N. I., L. Baecher-Steppan, D. M. Shepherd, J. A. Oughton, B. A. Vorderstrasse, G. K. DeKrey. 1996. Inhibition of TC-1 cytokine production, effector cytotoxic T lymphocyte development and alloantibody production by 2,3,7,8-tetrachlorodibenzo-p-dioxin. J. Immunol. 157: 2310-2319.
Kerkvliet, N. I.. 2002. Recent advances in understanding the mechanisms of TCDD immunotoxicity. Int. Immunopharmacol. 2: 277-291.
McMillan, B. J., S. N. McMillan, E. Glover, C. A. Bradfield. 2007. 2,3,7,8-tetrachlorodibenzo-p-dioxin induces premature activation of the KLF2 regulon during thymocyte development. J. Biol. Chem. 282: 12590-12597.
Fernandez-Salguero, P., T. Pineau, D. M. Hilbert, T. McPhail, S. S. Lee, S. Kimura, D. W. Nebert, S. Rudikoff, J. M. Ward, F. J. Gonzalez. 1995. Immune system impairment and hepatic fibrosis in mice lacking the dioxin-binding Ah receptor. Science 268: 722-726.
Kerkvliet, N. I., J. A. Oughton. 1993. Acute inflammatory response to sheep red blood cell challenge in mice treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD): phenotypic and functional analysis of peritoneal exudate cells. Toxicol. Appl. Pharmacol. 119: 248-257.
Doi, H., T. Baba, C. Tohyama, K. Nohara. 2003. Functional activation of arylhydrocarbon receptor (AhR) in primary T cells by 2,3,7,8-tetrachlorodibenzo-p-dioxin. Chemosphere 52: 655-662.
Ito, T., S. Tsukumo, N. Suzuki, H. Motohashi, M. Yamamoto, Y. Fujii-Kuriyama, J. Mimura, T. M. Lin, R. E. Peterson, C. Tohyama, K. Nohara. 2004. A constitutively active arylhydrocarbon receptor induces growth inhibition of jurkat T cells through changes in the expression of genes related to apoptosis and cell cycle arrest. J. Biol. Chem. 279: 25204-25210.
Laiosa, M. D., A. Wyman, F. G. Murante, N. C. Fiore, J. E. Staples, T. A. Gasiewicz, A. E. Silverstone. 2003. Cell proliferation arrest within intrathymic lymphocyte progenitor cells causes thymic atrophy mediated by the aryl hydrocarbon receptor. J. Immunol. 171: 4582-4591.
Staples, J. E., F. G. Murante, N. C. Fiore, T. A. Gasiewicz, A. E. Silverstone. 1998. Thymic alterations induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin are strictly dependent on aryl hydrocarbon receptor activation in hemopoietic cells. J. Immunol. 160: 3844-3854.
Van Grevenynghe, J., S. Rion, E. Le Ferrec, M. Le Vee, L. Amiot, R. Fauchet, O. Fardel. 2003. Polycyclic aromatic hydrocarbons inhibit differentiation of human monocytes into macrophages. J. Immunol. 170: 2374-2381.
Laupeze, B., L. Amiot, L. Sparfel, E. Le Ferrec, R. Fauchet, O. Fardel. 2002. Polycyclic aromatic hydrocarbons affect functional differentiation and maturation of human monocyte-derived dendritic cells. J. Immunol. 168: 2652-2658.
Kerkvliet, N. I., D. M. Shepherd, L. Baecher-Steppan. 2002. T lymphocytes are direct, aryl hydrocarbon receptor (AhR)-dependent targets of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD): AhR expression in both CD4+ and CD8+ T cells is necessary for full suppression of a cytotoxic T lymphocyte response by TCDD. Toxicol. Appl. Pharmacol. 185: 146-152.
Funatake, C. J., N. B. Marshall, L. B. Steppan, D. V. Mourich, N. I. Kerkvliet. 2005. Cutting edge: activation of the aryl hydrocarbon receptor by 2,3,7,8-tetrachlorodibenzo-p-dioxin generates a population of CD4+ CD25+ cells with characteristics of regulatory T cells. J. Immunol. 175: 4184-4188.
Lawrence, B. P., A. D. Roberts, J. J. Neumiller, J. A. Cundiff, D. L. Woodland. 2006. Aryl hydrocarbon receptor activation impairs the priming but not the recall of influenza virus-specific CD8+ T cells in the lung. J. Immunol. 177: 5819-5828.
Kathariou, S.. 2002. Listeria monocytogenes virulence and pathogenicity, a food safety perspective. J. Food Prot. 65: 1811-1829.
Centers for Disease Control (CDC) 2001. Preliminary FoodNet data on the incidence of foodbourne illnesses—selected states, United States, 2000. Morbid Mortal. Wkly. Rep. 50: 241-246.
Vazquez-Boland, J. A., M. Kuhn, P. Berche, T. Chakraborty, G. Dominguez-Bernal, W. Goebel, B. Gonzalez-Zorn, J. Wehland, J. Kreft. 2001. Listeria pathogenesis and molecular virulence determinants. Clin. Microbiol. Rev. 14: 584-640.
Cossart, P., J. Pizarro-Cerda, M. Lecuit. 2003. Invasion of mammalian cells by Listeria monocytogenes: functional mimicry to subvert cellular functions. Trends Cell Biol. 13: 23-31.
Sugita-Konishi, Y., K. Kobayashi, H. Naito, K. Miura, Y. Suzuki. 2003. Effect of lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin on the susceptibility to Listeria infection. Biosci. Biotechnol. Biochem. 67: 89-93.
Vos, J. G., J. G. Kreeftenberg, H. W. Engel, A. Minderhoud, L. M. Van Noorle Jansen. 1978. Studies on 2,3,7,8-tetrachlorodibenzo-p-dioxin induced immune suppression and decreased resistance to infection: endotoxin hypersensitivity, serum zinc concentrations and effect of thymosin treatment. Toxicology 9: 75-86.
Czuprynski, C. J., N. G. Faith. 2002. Sodium bicarbonate enhances the severity of infection in neutropenic mice orally inoculated with Listeria monocytogenes EGD. Clin. Diagn. Lab. Immunol. 9: 477-481.
Czuprynski, C. J., P. M. Henson, P. A. Campbell. 1984. Killing of Listeria monocytogenes by inflammatory neutrophils and mononuclear phagocytes from immune and nonimmune mice. J. Leukocyte Biol. 35: 193-208.
Murali-Krishna, K., J. D. Altman, M. Suresh, D. J. Sourdive, A. J. Zajac, J. D. Miller, J. Slansky, R. Ahmed. 1998. Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. Immunity 8: 177-187.
Pande, K., S. M. Moran, C. A. Bradfield. 2005. Aspects of dioxin toxicity are mediated by interleukin 1-like cytokines. Mol. Pharmacol. 67: 1393-1398.
Mocci, S., S. A. Dalrymple, R. Nishinakamura, R. Murray. 1997. The cytokine stew and innate resistance to L. monocytogenes. Immunol. Rev. 158: 107-114.
Hsieh, C. S., S. E. Macatonia, C. S. Tripp, S. F. Wolf, A. O’Garra, K. M. Murphy. 1993. Development of TH1 CD4+ T cells through IL-12 produced by Listeria-induced macrophages. Science 260: 547-549.
Dai, W. J., G. Kohler, F. Brombacher. 1997. Both innate and acquired immunity to Listeria monocytogenes infection are increased in IL-10-deficient mice. J. Immunol. 158: 2259-2267.
Moore, K. W., R. de Waal Malefyt, R. L. Coffman, A. O’Garra. 2001. Interleukin-10 and the interleukin-10 receptor. Annu. Rev. Immunol. 19: 683-765.
Pasche, B., S. Kalaydjiev, T. J. Franz, E. Kremmer, V. Gailus-Durner, H. Fuchs, M. Hrabe de Angelis, A. Lengeling, D. H. Busch. 2005. Sex-dependent susceptibility to Listeria monocytogenes infection is mediated by differential interleukin-10 production. Infect. Immun. 73: 5952-5960.
Tripp, C. S., S. F. Wolf, E. R. Unanue. 1993. Interleukin 12 and tumor necrosis factor α are costimulators of interferon γ production by natural killer cells in severe combined immunodeficiency mice with listeriosis, and interleukin 10 is a physiologic antagonist. Proc. Natl. Acad. Sci. USA 90: 3725-3729.
Vorderstrasse, B. A., L. B. Steppan, A. E. Silverstone, N. I. Kerkvliet. 2001. Aryl hydrocarbon receptor-deficient mice generate normal immune responses to model antigens and are resistant to TCDD-induced immune suppression. Toxicol. Appl. Pharmacol. 171: 157-164.
Foulds, K. E., M. J. Rotte, R. A. Seder. 2006. IL-10 is required for optimal CD8 T cell memory following Listeria monocytogenes infection. J. Immunol. 177: 2565-2574.
Harty, J. T., M. J. Bevan. 1995. Specific immunity to Listeria monocytogenes in the absence of IFN γ. Immunity 3: 109-117.
Harty, J. T., R. D. Schreiber, M. J. Bevan. 1992. CD8 T cells can protect against an intracellular bacterium in an interferon γ-independent fashion. Proc. Natl. Acad. Sci. USA 89: 11612-11616.