Activation of xenobiotic receptors: driving into the nucleus

H Li, H Wang - Expert opinion on drug metabolism & toxicology, 2010 - Taylor & Francis
H Li, H Wang
Expert opinion on drug metabolism & toxicology, 2010Taylor & Francis
Importance of the field: Xenobiotic receptors (XRs) play pivotal roles in regulating the
expression of genes that determine the clearance and detoxification of xenobiotics, such as
drugs and environmental chemicals. Recently, it has become increasingly evident that most
XRs shuttle between the cytoplasm and nucleus, and activation of such receptors is directly
associated with xenobiotic-induced nuclear import. Areas covered in this review: The scope
of this review covers research literature that discusses nuclear translocation and activation …
Importance of the field: Xenobiotic receptors (XRs) play pivotal roles in regulating the expression of genes that determine the clearance and detoxification of xenobiotics, such as drugs and environmental chemicals. Recently, it has become increasingly evident that most XRs shuttle between the cytoplasm and nucleus, and activation of such receptors is directly associated with xenobiotic-induced nuclear import.
Areas covered in this review: The scope of this review covers research literature that discusses nuclear translocation and activation of XRs, as well as unpublished data generated from this laboratory. Specific emphasis is given to the constitutive androstane receptor (CAR), the pregnane X receptor and the aryl hydrocarbon receptor.
What the readers will gain: A number of molecular chaperons presumably associated with cellular localization of XRs have been identified. Primary hepatocyte cultures have been established as a unique model retaining inactive CAR in the cytoplasm. Moreover, several splicing variants of human CAR exhibit altered cellular localization and chemical activation.
Take home message: Nuclear accumulation is an essential step in the activation of XRs. Although great strides have been made, much remains to be understood concerning the mechanisms underlying intracellular localization and trafficking of XRs, which involve both direct ligand-binding and indirect pathways.
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