Abstract
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.
Keywords
C
According to several reports, the CYP2A enzymes are present at high levels in the respiratory tract. For example, CYP2A3 is reported to be highly expressed in the rat nasal mucosa (Bereziat et al. 1995; Thornton-Manning et al. 1997; Gu et al. 1998). Su and co-workers (1996) have demonstrated expression of CYP2A5 in the mouse olfactory mucosa and lung, whereas CYP2A12 was not detected at these sites (Ding et al. 1996). In the human nasal mucosa and respiratory tract there is only low expression of CYP2A6, whereas the expression of CYP2A13 is more pronounced (Getchell et al. 1993; Fernandez-Salguero and Gonzalez 1995; Koskela et al. 1999; Dahlin et al. 2000; Ding and Kaminsky 2003).
Several substrates of the CYP2A enzymes appear to be toxic and carcinogenic for the nasal and respiratory epithelia. Coumarin, the major model substrate of CYP2A5 and CYP2A6, has recently been demonstrated to be an olfactory toxicant (Zhuo et al. 1999). CYP2A5 has also been reported to catalyze the metabolism of the potent olfactory toxicant dichlobenil (Eriksson and Brittebo 1991; Gu et al. 1998), the tobacco-specific procarcinogen and olfactory toxicant NNK[4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone] and the procarcinogens aflatoxin B1 and N-nitrosodi-ethylamine (Brittebo et al. 1981; Liu et al. 1996; Gu et al. 1998; Felicia et al. 2000).
The CYP levels in extrahepatic tissues are usually low and do not markedly influence the overall metabolism of drugs and chemicals in the body. Instead, the high expression of CYP2A enzymes in the nasal mucosa, along with the organ-specific damage induced by some of their substrates at this site, suggests that these enzymes may play a role in the mechanism of toxicity of these compounds. To better understand the possible role of the CYP2A5 in organ-selective metabolism and toxicity, the cellular sites of expression of the enzyme in the mouse respiratory tissues have been examined by ISH and IHC.
Because the CYP2A5 level in the liver is usually increased after exposure to various hepatotoxicants, we have also examined the effects of two olfactory toxicants on the CYP2A5 expression pattern in the olfactory mucosa (Honkakoski et al. 1988; Kojo et al. 1991,1998; Donato et al. 2000). Dichlobenil is known to induce permanent changes, such as respiratory metaplasia and fibrosis, in the lamina propria of the dorsomedial part of the olfactory region (Bergman et al. 2002). Methimazole is less potent but induces a more widespread necrosis in the neuroepithelium and Bowman's glands. However, this damage is rapidly repaired.
In addition, the effects of two typical hepatic CYP2A5 inducers, pyrazole and phenobarbital, on the morphology and CYP2A5 expression pattern in the olfactory mucosa were investigated in a mouse strain known to respond to these compounds. Phenobarbital is a transcriptional activator of CYP2A5, whereas pyrazole induces a protein, heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1), which stabilizes the CYP2A5 mRNA and increases the expression by increasing the half-life of mRNA (Thulke-Gross et al. 1998).
The results of the present investigation revealed a distinct expression of CYP2A5 in specific cell types in the upper and lower respiratory tract, the excretory ducts of salivary and nasal glands, and the nasolacrimal duct epithelium. The expression of CYP2A5 is in accordance with the previously suggested role of the enzyme in organ-specific toxicity of some protoxicants and may indeed determine the susceptibility of cells and tissues to compounds activated by CYP2A5. Furthermore, olfactory toxicants induced characteristic changes in the expression pattern, whereas hepatic CYP2A5 inducers did not change the expression pattern in the olfactory mucosa.
Materials and Methods
Chemicals
AdvanTaq DNA polymerase was purchased from Clontech Laboratories (Palo Alto, CA). Biotinylated goat anti-rabbit IgG, diaminobenzidine tetrahydrochloride (DAB), and streptavidin-HPR complex were obtained from Santa Cruz Biotechnology (Santa Cruz, CA) and also from Dakopatts AB (Älvsjö, Sweden). Bovine serum albumin (BSA) and pyrazole were purchased from Sigma-Aldrich Sweden AB (Stockholm, Sweden). Pertex was obtained from Histolab Product AB (Gothenburg, Sweden). Alkaline phosphatase-conjugated Fab fragment of sheep anti-DIG antibodies was obtained from Roche Diagnostics Scandinavia AB (Bromma, Sweden). Phenobarbital was purchased from Apoteket AB (Stockholm, Sweden). 2,6-Dichlorobenzonitrile (dichlobenil) was purchased from Aldrich Chemie (Steinheim, Germany) and methimazole was purchased from Sigma (St Louis, MO). Dimethyl sulfoxide (DMSO) was purchased from Merck (Darmstadt, Germany).
Antibody and Probe
A polyclonal antibody against the mouse CYP2A5 was raised in rabbits as previously described (Lang et al. 1989). The specificity of the antibody was tested by Western blotting and immunoinhibition analyses using mouse liver microsomes. The immunoblotting confirmed the presence of a major band corresponding to CYP2A5 (49.5 kD), while the immunoinhibition revealed that the highly homologous CYP2A4 with the same molecular mass was also recognized. It is not known if the antibody crossreacts with CYP2A12 or CYP2G1. The pUC9 plasmid containing CYP2A5 cDNA, used to produce the ISH probes, was kindly provided by Dr. Negishi (LRDT, NIEHS; Research Triangle Park, NC) (Squires and Negishi 1988).
Animals
Male (n = 3) and female (n = 3) NMRI mice were obtained from B&K Universal (Stockholm, Sweden). The mice were 9–10 weeks old and their weight ranged from 37 to 41 g (males) and from 30 to 32 g (females). In the study on olfactory toxicants, the female mice (n = 18) weighed 20–22 g. In addition, male DBA/2J (n = 9) were obtained from Möllegaard Glostrup, Denmark). The DBA/2J mice (20 g body weight) were 7 weeks old. The mice were housed at 22C with a 12-hr light/dark cycle and were given a standard pellet diet and tapwater ad libitum. The animals had at least 1 week of acclimatization. The animal studies were conducted in accordance with the guidelines of the Swedish National Board for Laboratory Animals (CFN) policy LSFS 1988:45. In addition, the studies were approved by the local Ethics Committee for Animal Research.
Untreated Mice
Male (n = 3) and female (n = 3) NMRI mice were anesthetized with gaseous CO2 and exsanguinated. Liver, lung, trachea, and salivary glands were excised and fixed in ice-cold 4% phosphate-buffered formaldehyde (pH 7.4). In addition, the entire nasal regions were dissected by removing the eyes, the integument, the lower jaws, and brain from the skull. The nasal passages were then gently perfused with phosphate-buffered formaldehyde via the nasopharyngeal duct. The nasal regions were decalcified with 5% EDTA in formaldehyde and cut into two blocks by slicing them transversely, perpendicularly to the hard palate through the first palate ridge of the mouse nasal cavity (Young 1981). The tissue blocks were embedded in low melting temperature paraffin. Transverse tissue sections (4 μm) were taken through the nose on levels 2, 3, and 4 according to the system of Young (1981) and were used for IHC and for ISH.
Effects of the Olfactory Toxicants Dichlobenil and Methimazole
Female NMRI mice were injected IP on days 0 and 3 with dichlobenil (25 mg/kg; n = 5) or methimazole (50 mg/kg; n = 5). Control mice were injected IP with DMSO (n = 4) or saline (n = 4). Four days or 2 weeks after the first administration the mice were anesthetized with gaseous CO2 and exsanguinated. The nasal region was excised, fixed, decalcified, and embedded in paraffin. Paraffin sections were used for IHC and histology. Sections used for histology were stained with hematoxylin-eosin or PAS (periodic acid-Schiff reagent).
Effects of the Hepatotoxicants Pyrazole and Phenobarbital
Male DBA/2J mice were injected IP with pyrazole (180 mg/kg; n = 3) three times (0, 24, 48 hr) or phenobarbital (80 mg/kg; n = 3). Control mice (n = 3) were injected IP with saline. At 24 hr after the last injection the mice were anesthetized with gaseous CO2 and exsanguinated. The nasal region and liver were excised and processed for IHC and histology as described above.
Immunohistochemistry
CYP2A5 was localized using the immunoperoxidase procedure with the streptavidin-horseradish peroxidase complex and DAB as the chromogen. Tissue sections were deparaffinized with xylene and hydrated gradually through a graded alcohol series (99.5%, 95%, and 70%). After washes with PBS and 3% Triton X-100 in PBS (PBS-T), to quench endogenous peroxidase activity, the sections were incubated for 30 min with 1% H2O2 in PBS-T. Nonspecific binding was blocked with 4% BSA in PBS for 1 hr. The sections were incubated overnight in a humidified chamber with the primary antibody (dilution 1:700) anti-CYP2A5. The next day the sections were rinsed and washed three times in PBS and PBS-T. The sections were then incubated for 1 hr with biotinylated secondary antibody (biotinylated goat anti-rabbit IgG) and for 30 min with streptavidin-HRP conjugate. The CYP2A5 was localized by the development of substrate-chromogen mixture (DAB). Some of the sections were counterstained with Gill's hematoxylin and were mounted immediately with Pertex. Staining specificity was appraised by substitution of the primary antibody with rabbit normal serum and of the secondary antibody with goat-normal serum.
In Situ Hybridization
Amplification of 1 ng of CYP2A5 cDNA was performed by the polymerase chain reaction (PCR) in a total volume of 50 μl, which contained sense and reverse primers (0.25 μM), 10 × PCR buffer (50 mM KCl, 10 mM Tris-HCl, 0.1% Triton X-100, and 2.5 mM MgCl2), dNTPs (0.2 μM), and 1 μl of DNA polymerase. The double-stranded DNA, including in its sequence the T7 promoter for posterior in vitro transcription of the antisense probe, was amplified using the 5′-TAATACGACTCACTATAGGGAGATGCCATA-3′ and 5′-ACCGCCACCATGCTGACCTCAGGA-3′ primers. Similarly, the primers for the sense probe were 5′-TAATACGACTCACTATAGGGAGAATGCTTGACCTCAGGACTCCT-3′ and 5′-TGCCATAAATAATATCTACT-3′ primers. These primers bind with the nucleotides 1670–1689 (T7 primers) and 1456–1475 of the CYP2A5 cDNA (Squires and Negishi 1988). The samples were incubated at 94C for 4 min and then amplified during 40 cycles (94C for 15 sec; 60C for 30 sec; 68C for 30 sec) with a final extension at 68C for 7 min. Amplified cDNA was ethanol-precipitated and dissolved in a final volume of 10 μl diethyl pyrocarbonate-treated water (DEPC). Single-stranded RNA probes (sense and antisense) labeled with digoxigenin-UTP were synthesized by in vitro transcription using T7 polymerase. ISH was carried out on paraffin-sectioned material according to the protocol described by Wilkinson (1992). In brief, the sections were dewaxed, rehydrated, and then pretreated with proteinase K (10 μg/ml in PBS) for 7 min. After fixation in 4% paraformaldehyde in PBS, the sense and antisense probes, diluted in hybridization buffer (50% formamide, 5 × SSC, 50 μg/ml yeast RNA, 1% SDS, and 50 μg/ml heparin), were added. After hybridization overnight at 65C, the sections were washed in 4 × SSC, followed by washes in 50% formamide, 5 × SSC, 1% SDS, and in 50% formamide and 2 × SSC at 65C. Sections were finally washed in 25 mM Tris-HCl, pH 7.5, containing 140 mM NaCl and 1% Tween-20. The pre-treatment and application of the alkaline phosphatase-conjugated Fab fragments of sheep anti-DIG antibodies, as well as the color development, were performed according to the manufacturer's recommendation (Roche Diagnostics Scandinavia). After color development, the sections were washed in PBS, dehydrated in 99.5% ethanol, cleared with xylene, and mounted in Pertex. Sections of the liver, nose, trachea, and lung were hybridized with the sense probe of CYP2A5 as negative controls.
Evaluation
The HC staining was performed twice in at least five sections per tissue for untreated NMRI mice and was performed three times with at least two sections per tissue for NMRI mice treated with test chemical or vehicle. The IHC staining was also performed twice in at least six sections per tissue for DBA/2J mice treated with test chemical or vehicle. The in situ staining was evaluated in one male and one female NMRI mouse in at least two sections per tissue except for the salivary glands, for which only one female mouse was evaluated. The evaluation of the staining was performed independently by two persons. The tissue sections used for IHC and ISH were photographed in a Leitz DM RXE microscope (Leica) using Nomarski differential interference technique with a digital camera (Hamamatsu; Tokyo, Japan). Images were processed in Adobe Photoshop 6.0 and Adobe Illustrator 10.
Results
Untreated Mice
Table 1 describes the evaluation of the cellular staining for CYP2A5 mRNA and protein in various tissues of NMRI mice. A general pattern of staining was clearly observed in various tissues among the individuals. In addition, there were no major qualitative differences in the staining pattern between male and female mice, except for a somewhat higher level of staining of the female liver. In the nasal passages, distinct staining for CYP2A5 mRNA and protein was detected in the apical part of the sustentacular cells and in the excretory duct and acini of Bowman's glands in the olfactory mucosa, and also in the transitional epithelium (Figures 1A and 2A). In the lateral parts of the olfactory region, the staining of the sustentacular cells and Bowman's glands was less intense.
Summary of immunohistochemistry and in situ hybridization of CYP2A5 in selected mouse tissues a
+ + +, intense staining; ++, moderate staining; +, weak staining; -, no staining.
In the basal part of the olfactory epithelium there was distinct IHC staining, most likely corresponding to the foot processes of the sustentacular cells, whereas there was no in situ staining at this site (Figures 1A and 2A). Otherwise, there was an almost identical localization of CYP2A5 mRNA and protein, indicating that regulation of expression of the enzyme at these sites is pretranslational and that the staining is specific.
The nasal respiratory mucosa presented no or weak staining in the epithelium and in the excretory ducts of seromucous glands in the lamina propria. There was also staining of excretory ducts of nasal glands around the maxillary sinuses and in the nasolacrimal duct epithelium (Figures 1C and 2C). In the lower respiratory tract there was staining of the apical parts of the columnar epithelium of the trachea (Figures 1E and 2E), bronchi, and bronchioles (Figures 1D and 2F). Staining of the apical part of the epithelium corresponded to non-ciliated Clara cells protruding into the lumen. Staining of the columnar epithelium decreased along the respiratory airways and the lowest level of staining occurred in the bronchioles. There was also staining of the striated and excretory ducts in the salivary glands (Figure 2D) and in the centrilobular region of the liver (data not shown).
No staining was observed in the lung parenchyma of the lung (Figure 1D), the nasal-associated lymphoid tissues, squamous epithelium of the oral cavity, acini of nasal glands around the maxillary sinuses, and acini of salivary glands. In addition, staining was not observed in the tissues after omission of the primary or the secondary antibody for the IHC studies and the use of the sense probe for the ISH (examples shown in Figures 1B and 2B).
Effects of the Olfactory Toxicants Dichlobenil and Methimazole
Dichlobenil. As previously reported, dichlobenil selectively targeted the dorsomedial part of the olfactory region whereas the lateral part was undamaged (Bergman et al. 2002). Four days after exposure to dichlobenil, the olfactory epithelium was thin and disorganized in the dorsomedial part of the olfactory region. The Bowman's glands were necrotic or had disappeared. At 2 weeks after administration there was an atypical ciliated respiratory-like epithelium and frequent invaginations of respiratory-like epithelium appeared in the dorsomedial region. In addition, there was fibrosis and the Bowman's glands had disappeared in the dorsomedial region. In the vehicle-treated controls the olfactory mucosa was intact.
In situ hybridization of CYP2A5 mRNA in selected tissues of NMRI mice. (
In the present study, 4 days after treatment with dichlobenil (Figure 3D) there was staining for CYP2A5 in some cells in the damaged and disorganized epithelium in the dorsomedial part of the olfactory region. There was no staining of the necrotic Bowman's glands in the lamina propria. Intact Bowman's glands in the undamaged lateral part of the olfactory region displayed weak staining, similar to that of control. At 2 weeks after administration, there was staining of the atypical respiratory-like epithelium and of the invaginations into the lamina propria. The stained cells were columnar. There was no staining of the fibrotic lamina propria in the dorsomedial part of the olfactory region (Figure 3F). Furthermore, there was no increased staining of the epithelium or glands in the border zone between damaged and undamaged mucosa 2 weeks after administration. In vehicle-treated NMRI mice (Figure 3B) the staining for CYP2A5 protein was similar to that observed in untreated NMRI mice.
Immunohistochemical staining of CYP2A5 in selected tissues of NMRI mice. (
Immunohistochemical staining of CYP2A5 in the olfactory mucosa of NMRI mice treated with the olfactory toxicants dichlobenil or methimazole. (
Methimazole. As previously reported, there was a thin and disorganized ol-factory epithelium in the ol factory region 4 days after administration of methimazole (Bergman et al. 2002). Most of the Bowman's glands had disappeared but a few scattered glands were observed. After 2 weeks the epithelium in the dorsomedial part was thin and disorganized and included cysts containing a homogeneous material, whereas the epithelium in the lateral part of the olfactory region was restored. In the lamina propria there were many Bowman's glands with an intact appearance. In the vehicle-treated controls the olfactory mucosa was intact.
In the present study, at 4 days after treatment with methimazole (Figure 3C) there was only weak staining for CYP2A5 in some cells of the regenerating olfactory epithelium but no staining of the necrotic lamina propria. At 2 weeks after administration (Figure 3E), staining was present in sustentacular cells in the regenerated olfactory epithelium and in some columnar cells of the disorganized epithelium in the dorsomedial part. The stained cells were focally distributed and in some regions the sustentacular cells did not display any stained foot processes. Most of the Bowman's glands were stained but scattered acini displayed no staining. In vehicle-treated NMRI mice (Figure 3B), the staining for CYP2A5 protein was similar to that observed in untreated NMRI mice.
Effects of the Hepatic CYP2A5 Inducers Pyrazole and Phenobarbital
Histological evaluation revealed that the olfactory mucosa of DBA/2J mice pretreated with pyrazole or phenobarbital was similar to that of saline-treated control animals. In all animals there was an intense PAS reaction of the contents of the Bowman's glands. In the livers of pyrazole- and phenobarbital-pretreated mice there was a decreased PAS reaction (marker for glycogen depletion) in the centrilobular parts. The decrease was most marked in the pyrazole-treated mice. In the saline-treated controls there was a homogeneous reaction for PAS throughout the liver.
The staining for CYP2A5 protein in the olfactory mucosa was not increased in the pyrazole- or phenobarbital-treated mice compared to the vehicle-treated controls. In the pyrazole-treated mice there was markedly increased staining of the CYP2A5 protein in the centrilobular region of the liver, especially in cells adjacent to the damaged centrilobular region. In the phenobarbital-treated mice there was only slightly increased staining of the centrilobular region of the liver. In the saline-treated DBA/2J mice, the localization of CYP2A5 protein in the nasal region and liver was similar to that observed in NMRI mice.
Discussion
The results of the present investigation revealed a highly specific expression of CYP2A5 mRNA and protein in the upper and lower respiratory tract, the excretory ducts of salivary and nasal glands, and in the nasolacrimal duct epithelium. There was a predominant expression of CYP2A5 in the olfactory mucosa; the apical parts of the sustentacular cells and the acini and excretory ducts of Bowman's glands expressed CYP2A5 mRNA and protein. Interestingly, there was no staining for mRNA in the basal part of the olfactory epithelium, although the protein was present at this site, suggesting a transfer of CYP2A5 protein from the apical part of the sustentacular cells to the foot processes. Pretreatment with the hepatic CYP2A5 inducers pyrazole and phenobarbital did not change the expression pattern of the enzyme in the olfactory mucosa, whereas the olfactory toxicants dichlobenil and methimazole induced characteristic changes in the expression pattern at this site.
The predominant expression of CYP2A5 in the mouse olfactory mucosa is in agreement with previous studies demonstrating that CYP2A5 is a major CYP in this tissue (Walters et al. 1993; Thornton-Manning et al. 1997; Gu et al. 1998). It cannot be excluded that the antibody or the cRNA probe used in this study might crossreact with CYP2A12 and CYP2A4. However, these isoforms are reported to be expressed at much lower levels than CYP2A5 in the mouse olfactory mucosa (Ding et al. 1996). Therefore, the signals detected in the olfactory mucosa are a bona fide reflection of the CYP2A5 level, with only a minor contribution of other CYP2A isoforms. No data are available on the cellular expression of CYP2A12 and CYP2A4 in other sites of the respiratory tract. Gu and co-workers (1998) have reported that several antibodies against CYP2A also react with CYP2G1. This has, however, not been determined for the antibody used in this study.
The predominant expression of CYP2A5 and some minor CYP forms in the olfactory mucosa may be of importance for the protection of neurons in the olfactory pathways against chemically induced damage (Adams et al. 1991; Chen et al. 1992). A rapid biotransformation would increase the clearance of airborne compounds in the neuroepithelium but might also lead to a decreased transfer of potential neurotoxicants to the brain via the olfactory pathways. The olfactory neurons have dendrites projecting into the olfactory mucus and axons projecting directly into the olfactory bulb. This connection may therefore be a portal of entry of drugs and toxicants into the brain, thus circumventing the blood-brain barrier. A significant uptake of some drugs and chemicals has been reported in the ipsilateral olfactory bulb after a unilateral intranasal instillation (Dahlin et al. 2000; Bergstrom et al. 2002).
Previous studies have demonstrated a high rate of metabolic activation of some CYP2A5 and CYP2A3 substrates, such as the herbicide dichlobenil and the tobacco-specific carcinogen NNK, into reactive intermediates in the rodent olfactory mucosa (Eriksson and Brittebo 1991; Ding et al. 1996; Gu et al. 1998). Light microscopic autoradiography studies have revealed a preferential localization of protein adducts of radio-labeled dichlobenil and NNK in Bowman's glands (Tjalve et al. 1985; Brandt et al. 1990). Furthermore, IHC studies have reported a selective localization of NNK DNA adducts in these glands (Van Benthem et al. 1994). The alkylation of vital macromolecules in the Bowman's glands may result in a changed or impaired function leading to detrimental consequences, and both dichlobenil and NNK are reported to initially damage these glands (Belinsky et al. 1987; Brandt et al. 1990).
The present study revealed that pretreatment with the olfactory toxicants dichlobenil and methimazole induced characteristic changes in the olfactory expression pattern of CYP2A5. At 4 days after treatment with dichlobenil or methimazole there was no expression of CYP2A5 in the damaged Bowman's glands in the lamina propria. At 2 weeks after treatment with dichlobenil there was no expression of the enzyme in the fibrotic lamina propria. In contrast, 2 weeks after treatment with methimazole the expression of CYP2A5 in the regenerated Bowman's glands was similar to that in the controls, confirming that methimazole-induced effects at this site are reversible.
Interestingly, our study also revealed that there was distinct CYP2A5 expression in the damaged and disorganized epithelium 4 days after the administration of dichlobenil and methimazole. At 2 weeks after treatment with methimazole, the neuroepithelium was still thin and disorganized in the dorsomedial part. CYP2A5 was expressed in sustentacular cells in the restored part and in columnar cells in the disorganized epithelium. A slow recovery of CYP2A expression in the sustentacular cells has also been observed in rats 4–6 weeks after treatment with the reversible olfactory toxicant methyl bromide (Schwob et al. 1995). However, no recovery of CYP2A expression was reported in methyl bromide-induced respiratory-like epithelium in the olfactory region of rats (Schwob et al. 1995). In contrast, the present results demonstrated that the dichlobenil-induced respiratory-like epithelium expressed CYP2A5. At 2 weeks after treatment with dichlobenil there was expression of CYP2A5 in the atypical respiratory-like epithelium and in invaginations of the epithelium into the lamina propria. In olfactory mucosa recovering from a toxic insult, the sustentacular cells have been suggested to originate from both the Bowman's glands and basal cells (Huard et al. 1998). Because no intact Bowman's glands were present in the fibrotic lamina propria, these glands are most likely not stem cells for the respiratory-like epithelium expressing CYP2A5 in dichlobenil-treated mice. These respiratory-like cells could thus originate from undamaged basal cells, but the molecular mechanisms and lineage relationships involved in the respiratory metaplasia are unclear. In addition, because the respiratory epithelium of vehicle-treated mice showed negligible expression of CYP2A5, it seems less likely that the CYP2A5-expressing cells in the respiratory-like epithelium are related to the columnar cells in the normal respiratory epithelium.
Recent studies have indicated that the induction of hepatic CYP2A5 by typical inducers is not due to the compounds per se but instead is related to hepatotoxic effects (Gilmore et al. 2003). The present results demonstrated that the hepatic CYP2A5 inducers pyrazole and phenobarbital neither damaged the olfactory mucosa nor changed the expression of CYP2A5 at this site. The lack of induction may be related to the lack of toxicity of these compounds in the olfactory mucosa. Gilmore and co-workers (2003) have suggested that an increased CYP2A5 expression in areas adjacent to damaged hepatocytes may be related to oxidative injury in these cells. Increased CYP2A6 expression has also been found in areas adjacent to liver tumors (Kojo et al. 1998). Previous studies have revealed a distinct border zone with markedly increased neurogenesis between damaged and undamaged parts of the olfactory region 2 weeks after exposure to the olfactory toxicant dichlobenil (Bergman et al. 2002). However, there was no increase in expression of CYP2A5 in the neuroepithelium or Bowman's glands in this border zone of dichlobenil-treated mice.
Site-selective and region-specific differences are often reported for CYPs in the respiratory tissues. The present study also revealed a decreasing expression of CYP2A5 mRNA and protein along the epithelial linings of the trachea, bronchi, and bronchioles. CYP2A5 expression was not observed in the lung alveolar region, indicating that alveolar cells, endothelial cells, and macrophages do not express this enzyme. The metabolism of CYP2A5 substrates is generally low in the lung, but it should be noted that a distinct localization of protein adducts of some CYP2A5/3 substrates, dichlobenil and NNK, in the epithelium of the trachea and bronchi/bronchioles of rodents has been reported (Bakke et al. 1988). NNK is also known to induce tumors in the lung of rodents (Belinsky et al. 1990).
The present study also revealed a weak expression in the excretory ducts of seromucous glands in the nasal septum as well as in sublingual and submandibular glands, whereas no staining occurred in the acini. There was also CYP2A5 expression in the squamous epithelium in the nasolacrimal duct and weak expression in the excretory ducts of the glands around the maxillary sinuses. Little is known about the metabolism and effects of chemicals in excretory ducts. In the epithelium of the rat nasolacrimal duct, a selective localization of NNK has been reported (Lofberg et al. 1982), suggesting that a biotransformation can occur at this site.
In summary, the results of the present study demonstrated a cell-specific expression of CYP2A5 mRNA and protein in the mouse respiratory tract, excretory ducts of nasal and salivary glands, and the nasolacrimal duct epithelium. In the nasal region differential expression was observed. There was marked expression in sustentacular cells and Bowman's glands in the olfactory mucosa, whereas in the respiratory mucosa there was no or only weak expression. Typical hepatic CYP2A5 inducers did not change the expression pattern in the olfactory mucosa. In contrast, olfactory toxicants induced characteristic changes. The damaged Bowman's glands did not express CYP2A5, whereas the damaged epithelium expressed the enzyme. The results also revealed a decreasing expression of CYP2A5 along the epithelial linings of trachea and lower respiratory tract. The cell-specific expression of CYP2A5 indicates that this CYP isoform plays a key role in determining the susceptibility of the respiratory tract after exposure to air- and blood-borne protoxicants and procarcinogens. Indeed, previous reports have demonstrated a cell-specific localization of protein and DNA adducts of some CYP2A5 substrates in the respiratory tract.
Footnotes
Acknowledgements
Supported by The Swedish Research Council (EBB) and The Italian National Council of Research (EP).