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Deletion of the aryl hydrocarbon receptor enhances the inflammatory response to Leishmania major infection.

Abstract
The aryl hydrocarbon receptor (AhR) is a ligand-activated receptor that mediates the toxicity of environmental pollutants, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Recently, it has been shown that the AhR plays a role in immune and inflammatory regulation. However, most of these studies are based on the activation of AhR by exogenous ligands. Therefore, in the present study, we addressed the role of this transcription factor, in the absent of exogenous ligand, on the immune response to Leishmania major infection. Our results indicate that inactivation of the AhR results in an alteration of the levels of several cytokines. Lymph node cells from infected Ahr-null animals displayed an increase in IFNγ and IL-12 levels, together with a decrease in IL-4 and IL-10 levels compared to wild-type (wt) mice. Ahr-null mice also presented higher serum levels of the pro-inflammatory cytokine TNF-α prior to parasite inoculation and during infection compared to wt mice. Moreover, a 30% decrease in the population of T(reg) cells was observed in Ahr-null mice. This decrease was associated with a reduction in Foxp3 mRNA levels. Finally, the alteration in the cytokine profile results in a better resolution of the L. major infection.
AuthorsGuillermo Elizondo, Miriam Rodríguez-Sosa, Elizabet Estrada-Muñiz, Frank J Gonzalez, Libia Vega
JournalInternational journal of biological sciences (Int J Biol Sci) Vol. 7 Issue 9 Pg. 1220-9 ( 2011) ISSN: 1449-2288 [Electronic] Australia
PMID22110376 (Publication Type: Journal Article)
Chemical References
  • Antigens, Protozoan
  • Cytokines
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Interleukin-17
  • Polychlorinated Dibenzodioxins
  • Polycyclic Aromatic Hydrocarbons
  • Receptors, Aryl Hydrocarbon
  • Interleukin-10
  • Interleukin-4
Topics
  • Animals
  • Antigens, Protozoan (immunology)
  • Cytokines (metabolism)
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Forkhead Transcription Factors (metabolism)
  • Interleukin-10 (metabolism)
  • Interleukin-17 (metabolism)
  • Interleukin-4 (metabolism)
  • Leishmania major (immunology, pathogenicity)
  • Leishmaniasis, Cutaneous (immunology, parasitology)
  • Mice
  • Mice, Knockout
  • Polychlorinated Dibenzodioxins (pharmacology)
  • Polycyclic Aromatic Hydrocarbons (metabolism)
  • Polymerase Chain Reaction
  • Receptors, Aryl Hydrocarbon (genetics, metabolism)
  • T-Lymphocytes, Regulatory (immunology)

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