Aryl hydrocarbon receptor

From WikiMD's Food, Medicine & Wellness Encyclopedia

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Aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor that is involved in the regulation of biological responses to planar aromatic (hydrocarbons). AHR is a member of the basic helix-loop-helix (bHLH)–Per-Arnt-Sim (PAS) superfamily of transcription factors. This receptor is best known for its role in mediating the toxic effects of dioxin and related compounds, but it also plays important roles in development, immune system function, and homeostasis.

Structure and Function[edit | edit source]

The AHR protein has several domains critical for its function: a bHLH domain for DNA binding, two PAS domains for ligand binding and dimerization, and a transactivation domain. Upon binding to its ligands, which can be endogenous or exogenous, AHR translocates from the cytoplasm to the nucleus, where it dimerizes with the AHR nuclear translocator (ARNT). This AHR/ARNT complex then binds to xenobiotic response elements (XREs) in the DNA, leading to the transcription of genes involved in xenobiotic metabolism, such as those encoding for cytochrome P450 enzymes.

Ligands[edit | edit source]

AHR ligands include a wide variety of environmental pollutants, such as dioxins, polycyclic aromatic hydrocarbons (PAHs), and certain plant flavonoids. These compounds are generally planar and hydrophobic, allowing them to easily diffuse across cell membranes and bind to AHR. The diversity of AHR ligands suggests that AHR may have evolved as a sensor for foreign compounds, facilitating the organism's ability to respond to environmental challenges.

Biological Roles[edit | edit source]

Beyond its role in xenobiotic metabolism, AHR is involved in several physiological processes. It has been implicated in the regulation of cell proliferation and differentiation, apoptosis, and immune system function. In the immune system, AHR influences the behavior of various cell types, including T cells and dendritic cells, affecting both innate and adaptive immunity. AHR also plays a role in the development of certain organs, such as the liver and the lung.

Pathological Roles[edit | edit source]

While AHR plays crucial roles in metabolism and normal physiological processes, its activation by toxic environmental ligands can lead to adverse health effects. For example, exposure to high levels of dioxins, which are potent AHR ligands, has been associated with various diseases, including cancer, developmental defects, and immune system dysfunction. The role of AHR in mediating the effects of environmental toxins has made it a target of interest for research into the prevention and treatment of these conditions.

Research and Therapeutic Potential[edit | edit source]

Given its central role in mediating responses to environmental toxins and its involvement in various physiological processes, AHR is a target of ongoing research. Scientists are exploring the potential of modulating AHR activity to treat diseases related to its dysfunction. For example, AHR antagonists are being investigated for their potential to mitigate the toxic effects of dioxin exposure. Conversely, AHR agonists may have therapeutic potential in diseases where AHR activation is beneficial, such as certain autoimmune disorders.



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Contributors: Prab R. Tumpati, MD