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Cell-specific expression of CYP2A5 in the mouse respiratory tract: effects of olfactory toxicants.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Pharmacy, Department of Pharmaceutical Biosciences.
Uppsala University, Disciplinary Domain of Science and Technology, Biology, Department of Organism Biology, Environmental Toxicology.
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2003 (English)In: Journal of Histochemistry and Cytochemistry, ISSN 0022-1554, E-ISSN 1551-5044, Vol. 51, no 11, 1545-1555 p.Article in journal (Refereed) Published
Abstract [en]

We performed a detailed analysis of mouse cytochrome P450 2A5 (CYP2A5) expression by in situ hybridization (ISH) and immunohistochemistry (IHC) in the respiratory tissues of mice. The CYP2A5 mRNA and the corresponding protein co-localized at most sites and were predominantly detected in the olfactory region, with an expression in sustentacular cells, Bowman's gland, and duct cells. In the respiratory and transitional epithelium there was no or only weak expression. The nasolacrimal duct and the excretory ducts of nasal and salivary glands displayed expression, whereas no expression occurred in the acini. There was decreasing expression along the epithelial linings of the trachea and lower respiratory tract, whereas no expression occurred in the alveoli. The hepatic CYP2A5 inducers pyrazole and phenobarbital neither changed the CYP2A5 expression pattern nor damaged the olfactory mucosa. In contrast, the olfactory toxicants dichlobenil and methimazole induced characteristic changes. The damaged Bowman's glands displayed no expression, whereas the damaged epithelium expressed the enzyme. The CYP2A5 expression pattern is in accordance with previously reported localization of protein and DNA adducts and the toxicity of some CYP2A5 substrates. This suggests that CYP2A5 is an important determinant for the susceptibility of the nasal and respiratory epithelia to protoxicants and procarcinogens.

Place, publisher, year, edition, pages
2003. Vol. 51, no 11, 1545-1555 p.
Keyword [en]
Animals, Aryl Hydrocarbon Hydroxylases/*biosynthesis, Environmental Pollutants/*toxicity, Enzyme Induction, Female, Immunohistochemistry, In Situ Hybridization, Male, Methimazole/toxicity, Mice, Mice, Inbred DBA, Mixed Function Oxygenases/*biosynthesis, Nasolacrimal Duct/cytology/drug effects/metabolism, Nitriles/toxicity, Olfactory Mucosa/cytology/drug effects/metabolism, Phenobarbital/toxicity, Pyrazoles/toxicity, Respiratory System/cytology/drug effects/*metabolism, Salivary Glands/cytology/drug effects/metabolism, Support, Non-U.S. Gov't
National Category
Biological Sciences
Research subject
Ecotoxicology
Identifiers
URN: urn:nbn:se:uu:diva-67120PubMedID: 14566026OAI: oai:DiVA.org:uu-67120DiVA: diva2:95031
Available from: 2008-11-28 Created: 2008-11-28 Last updated: 2017-11-28Bibliographically approved

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PubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=14566026&dopt=Citationhttp://www.jhc.org/cgi/content/abstract/51/11/1545

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Piras, ElenaBergström, UlrikaLang, MattiBrittebo, Eva B.

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