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Influence of oxidative stress on aryl hydrocarbon receptor signaling

thesis
posted on 2024-09-03, 04:28 authored by Afshin Mohammadibardbori

The aryl hydrocarbon receptor (AHR), a multifunctional protein and a key regulator of drug metabolizing enzymes, belongs to the basic-helix-loop-helix (bHLH)/PAS (Per-Arnt-Sim) super-family of transcription factors. The AHR responds to exogenous and endogenous chemicals by induction or repression of a large number of genes involved in many physiological processes and normal development.

The diverse spectrum of AHR activators from well-known planar hydrophobic halogenated aromatic hydrocarbons (HAHs) to chemical compounds whose structure and physicochemical properties are very different from classical AHR ligands suggests that the AHR has a tremendously promiscuous ligand binding pocket. Due to the absence of a 3D structure of the ligand binding domain, promiscuity of the AHR has remained elusive. However, increasing experimental evidence indicate that the non-typical AHR ligands might activate the AHR signaling pathway indirectly by inhibiting the metabolic turnover of an endogenous ligand of the AHR. Therefore, the objective of this thesis was to characterize the inhibition of degradation of 6-formylindolo[3,2-b]carbazole (FICZ), the suggested natural high affinity AHR ligand, as a mechanism that could explain the earlier described agonistic properties of structurally very diverse AHR activators. The obtained results show that FICZ is a potent AHR agonist in vitro and in vivo which can distribute to the body through systemic circulation and induce cytochrome P450 1A1 (CYP1A1) the prototypical AHR target in various organs. The studies presented in this thesis demonstrate that if the metabolic clearance of FICZ is compromised, femtomolar concentrations of FICZ are sufficient to activate AHR signaling.

The AHR signaling pathway seems to be sensitive to oxidative stress but the redox regulation of AHR has not been well characterized. Studies on dioxin and other reactive oxygen species (ROS) producing agents have demonstrated that the AHR is a mediator of oxidative stress. Indeed, AHR works in close concert with the master regulator of antioxidant responses, nuclear factor (erythroid-derived 2)-like 2 (Nrf2). Multiple sources of ROS appear to be involved in modulating AHR signaling and probably via three major systems, microsomes, mitochondria and NADPH oxidase enzymes (NOXs). Furthermore, it has been observed that many environmental pollutants, including metals and other NOX-activators increase the levels of the diffusible molecule hydrogen peroxide (H2O2) and change the cellular redox status and thereby interfere with cell growth kinetics and the endogenous functions of the AHR.

To increase the understanding of downstream adaptive responses to oxidative stress, including up-regulation of antioxidant genes and modulation of AHR signaling was another objective of this work. The findings demonstrate that superoxide anion (O2−.) or H2O2 produced by NOXs can negatively and positively modulate the AHR signaling pathway. The importance of cellular redox levels which can influence endogenously activated AHR signaling broadens our earlier knowledge and explains why many oxidants behave both as AHR antagonists and agonists.

In summary, this thesis extends the mechanistic understanding of the promiscuity of AHR and provides important information with regard to the redox regulation of AHR endogenous signaling.

List of scientific papers

I. Wincent E, Bengtsson J, Mohammadi Bardbori A, Alsberg T, Luecke S, Rannug U, Rannug A. (2012). Inhibition of cytochrome P4501-dependent clearance of the endogenous agonist FICZ as a mechanism for activation of the aryl hydrocarbon receptor. Proc Natl Acad Sci U S A. 109(12):4479-84.
https://doi.org/10.1073/pnas.1118467109

II. Mohammadi-Bardbori A, Bengtsson J, Rannug U, Rannug A, Wincent E. (2012). Quercetin, resveratrol and curcumin are indirect activators of the aryl hydrocarbon receptor (AHR). Chem Res Toxicol. 17;25(9):1878-84.
https://doi.org/10.1021/tx300169e

III. Mohammadi-Bardbori A, Vikström Bergander L, Rannug U, and Rannug A. NADPH oxidase has a central role in aryl hydrocarbon receptor signaling and regulation of cell growth by arsenic, cadmium, mercury and nickel. [Manuscript]

History

Defence date

2013-06-05

Department

  • Institute of Environmental Medicine

Publisher/Institution

Karolinska Institutet

Main supervisor

Rannug, Agneta

Publication year

2013

Thesis type

  • Doctoral thesis

ISBN

978-91-7549-163-9

Number of supporting papers

3

Language

  • eng

Original publication date

2013-05-13

Author name in thesis

Mohammadi Bardbori, Afshin

Original department name

Institute of Environmental Medicine

Place of publication

Stockholm

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