Xenobiotic Receptors and Their Mates in Atopic Dermatitis

Int J Mol Sci. 2019 Aug 29;20(17):4234. doi: 10.3390/ijms20174234.

Abstract

Atopic dermatitis (AD) is the most common inflammatory skin disease worldwide. It is a chronic, relapsing and pruritic skin disorder which results from epidermal barrier abnormalities and immune dysregulation, both modulated by environmental factors. AD is strongly associated with asthma and allergic rhinitis in the so-called 'atopic march.' Xenobiotic receptors and their mates are ligand-activated transcription factors expressed in the skin where they control cellular detoxification pathways. Moreover, they regulate the expression of genes in pathways involved in AD in epithelial cells and immune cells. Activation or overexpression of xenobiotic receptors in the skin can be deleterious or beneficial, depending on context, ligand and activation duration. Moreover, their impact on skin might be amplified by crosstalk among xenobiotic receptors and their mates. Because they are activated by a broad range of endogenous molecules, drugs and pollutants owing to their promiscuous ligand affinity, they have recently crystalized the attention of researchers, including in dermatology and especially in the AD field. This review examines the putative roles of these receptors in AD by critically evaluating the conditions under which the proteins and their ligands have been studied. This information should provide new insights into AD pathogenesis and ways to develop new therapeutic interventions.

Keywords: AHR; LXR; PPAR; PXR; atopic dermatitis; inflammation; pollution; skin; xenobiotic receptors.

Publication types

  • Review

MeSH terms

  • Asthma / genetics
  • Asthma / immunology
  • Asthma / metabolism
  • Dermatitis, Atopic / genetics
  • Dermatitis, Atopic / immunology
  • Dermatitis, Atopic / metabolism*
  • Eczema / genetics
  • Eczema / immunology
  • Eczema / metabolism
  • Epidermis / immunology
  • Epidermis / metabolism
  • Epidermis / pathology
  • Gene Expression Regulation / immunology
  • Ligands
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Rhinitis, Allergic / genetics
  • Rhinitis, Allergic / immunology
  • Rhinitis, Allergic / metabolism
  • Skin / immunology
  • Skin / metabolism*
  • Skin / pathology
  • Xenobiotics / metabolism*

Substances

  • Ligands
  • Receptors, Cytoplasmic and Nuclear
  • Xenobiotics