Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

The arylhydrocarbon receptor repressor (AhRR): structure, expression, and function.

Thomas Haarmann-Stemmann1, Josef Abel

  • 1Arbeitsgruppe Toxikologie, Institut für umweltmedizinische Forschung (IUF) an der Heinrich-Heine-Universität Düsseldorf gGmbH, Auf'm Hennekamp 50, D-40225 Düsseldorf, Germany. haarmann@uni-dusseldorf.de

Biological Chemistry
|September 16, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Toxin of the Year: Airborne PM<sub>2.5</sub>.

Dermatitis : contact, atopic, occupational, drug·2026
Same author

Regional and size-dependent effects of ambient agricultural particulate matter on Ah-receptor activity and inflammatory responses in human U937 macrophages.

Inhalation toxicology·2026
Same author

Erlotinib and Leflunomide Disrupt 6-Formylindolo[3,2-b]Carbazole Metabolism and Sensitize Keratinocytes to UVA Radiation-Induced Apoptosis.

Photodermatology, photoimmunology & photomedicine·2026
Same author

Evidence For a Fibrogenic Interaction Between the Aryl Hydrocarbon Receptor and the Wnt/β-Catenin Pathways in Human Keratinocytes and Fibroblasts.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology·2026
Same author

[Environmental dermatology].

Dermatologie (Heidelberg, Germany)·2026
Same author

The aryl hydrocarbon receptor: structure, signaling, physiology and pathology.

Signal transduction and targeted therapy·2026
Same journal

Neuronal membrane organization by the submembranous spectrin-ankyrin scaffold: evolution, specialization and disease.

Biological chemistry·2026
Same journal

Golgi-associated membrane scaffolds: roles in health and disease.

Biological chemistry·2026
Same journal

Mechanistic insights on spatiotemporal control of Ras-signaling.

Biological chemistry·2026
Same journal

Cysteine cathepsin proteases in apicomplexan parasites.

Biological chemistry·2026
Same journal

Electron donating and withdrawing groups affect the antioxidant activity of 4'-aminochalcones on gentamicin-induced kidney cell injury.

Biological chemistry·2026
Same journal

CNKSR2 scaffold function in the mammalian nervous system.

Biological chemistry·2026
See all related articles

The aryl hydrocarbon receptor repressor (AhRR) is a recently identified gene. Its role in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) toxicity and its in vivo function remain unclear, necessitating further research.

Area of Science:

  • Environmental Toxicology
  • Molecular Biology
  • Cell Signaling

Background:

  • The aryl hydrocarbon receptor (AhR) pathway mediates cellular responses to environmental chemicals like 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD).
  • While the AhR's role in TCDD toxicity is understood, the function of the aryl hydrocarbon receptor repressor (AhRR) in this pathway is largely unknown.
  • AhRR is ubiquitously expressed in mammalian tissues and its expression is modulated by AhR ligands, showing cell-, tissue-, and species-specific patterns.

Purpose of the Study:

  • To review the current knowledge on AhRR.
  • To highlight the unclear role of AhRR in TCDD-stimulated AhR signaling.
  • To stimulate further research into AhRR's physiological and toxicological significance.

Main Methods:

  • Literature review of existing studies on AhRR.

Related Experiment Videos

  • Analysis of AhRR expression patterns in various contexts.
  • Examination of proposed inhibitory activity of AhRR on AhR signaling.
  • Main Results:

    • AhRR expression is widespread but exhibits significant cell-, tissue-, and species-specificity.
    • Overexpression studies suggest AhRR may inhibit AhR signaling.
    • There is a lack of in vivo data to confirm AhRR's functional activity.

    Conclusions:

    • The precise physiological function of AhRR is yet to be elucidated.
    • Further in vivo studies are required to understand AhRR's role in dioxin toxicity.
    • Research into AhRR is crucial for a comprehensive understanding of AhR signaling and TCDD-induced effects.