TY - JOUR
T1 - Regulation of cytochrome P450 gene expression in the olfactory mucosa
AU - Ling, Guoyu
AU - Gu, Jun
AU - Genter, Mary Beth
AU - Zhuo, Xiaoliang
AU - Ding, Xinxin
N1 - Funding Information:
We thank Drs. Laurence Kaminsky and Adriana Verschoor for critical readings of the manuscript. This work was supported in part by National Institutes of Health research grants CA092596 and ES07462 (to X.D.), and AG13837, DC006505, and ES08788 (to M.B.G.).
PY - 2004/4/15
Y1 - 2004/4/15
N2 - The mammalian olfactory mucosa (OM) is unique among extrahepatic tissues in having high levels, and tissue-selective forms, of cytochrome P450 (CYP) enzymes. These enzymes may have important toxicological implications, as well as biological functions, in this chemosensory organ. In addition to a tissue-selective, abundant expression of CYP1A2, CYP2A, and CYP2G1, some of the OM CYPs are also known to have an early developmental expression, a resistance to xenobiotic inducers, and a lack of responsiveness to circadian rhythm. Efforts to fully characterize the regulation of CYP expression in the OM, and to identify the underlying mechanisms, are important for our understanding of the physiological functions and toxicological significance of these biotransformation enzymes, and may also shed unique light on the general mechanisms of CYP regulation. The aim of this mini-review is to provide a summary of current knowledge of the various modes of regulation of CYPs expressed in the OM, an update on our mechanistic studies on tissue-selective CYP expression, and a review of the literature on xenobiotic inducibility of OM CYPs. Our goal is to stimulate further studies in this exciting research area, which is of considerable importance, in view of the constant exposure of the human nasal tissues to inhaled, as well as systemically derived, chemicals, the prevalence of olfactory system damage in individuals with neurodegenerative diseases, and the current uncertainty in risk assessments for potential olfactory toxicants.
AB - The mammalian olfactory mucosa (OM) is unique among extrahepatic tissues in having high levels, and tissue-selective forms, of cytochrome P450 (CYP) enzymes. These enzymes may have important toxicological implications, as well as biological functions, in this chemosensory organ. In addition to a tissue-selective, abundant expression of CYP1A2, CYP2A, and CYP2G1, some of the OM CYPs are also known to have an early developmental expression, a resistance to xenobiotic inducers, and a lack of responsiveness to circadian rhythm. Efforts to fully characterize the regulation of CYP expression in the OM, and to identify the underlying mechanisms, are important for our understanding of the physiological functions and toxicological significance of these biotransformation enzymes, and may also shed unique light on the general mechanisms of CYP regulation. The aim of this mini-review is to provide a summary of current knowledge of the various modes of regulation of CYPs expressed in the OM, an update on our mechanistic studies on tissue-selective CYP expression, and a review of the literature on xenobiotic inducibility of OM CYPs. Our goal is to stimulate further studies in this exciting research area, which is of considerable importance, in view of the constant exposure of the human nasal tissues to inhaled, as well as systemically derived, chemicals, the prevalence of olfactory system damage in individuals with neurodegenerative diseases, and the current uncertainty in risk assessments for potential olfactory toxicants.
KW - 2,6-dichlorobenzonitrile
KW - 3-MC
KW - 3-methylcholanthrene
KW - AhR
KW - BaP
KW - CYP
KW - DCBN
KW - LCR
KW - LSF
KW - NFI
KW - OM
KW - aryl hydrocarbon receptor
KW - benzo[a]pyrene
KW - cytochrome P450
KW - locus control region
KW - lung-specific factor
KW - mEH
KW - microsomal epoxide hydrolase
KW - nuclear factor 1
KW - olfactory mucosa
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U2 - 10.1016/j.cbi.2004.02.003
DO - 10.1016/j.cbi.2004.02.003
M3 - Review article
C2 - 15135081
AN - SCOPUS:2342512149
SN - 0009-2797
VL - 147
SP - 247
EP - 258
JO - Chemico-Biological Interactions
JF - Chemico-Biological Interactions
IS - 3
ER -