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Expression of Prostaglandin D2 Synthase in Activated Eosinophils in Nasal Polyps

Expression of Prostaglandin D2 Synthase in Activated Eosinophils in Nasal Polyps Abstract Objective To clarify the relationship between prostaglandin D2 production and eosinophil accumulation. Design Screening and diagnostic tests. Subjects Nineteen patients with chronic rhinosinusitis. Interventions Nasal polyps were obtained from 19 patients at endoscopic sinus surgery. Eosinophils in nasal polyps were counted after hematoxylin-eosin staining and immunostaining with antibodies against 2 eosinophil markers—major basic protein and EG2. Hematopoietic prostaglandin D2 synthase (HPGDS) expression was examined by semiquantitative Western blot analysis and by immunohistochemical staining with anti-HPGDS antibody. Results Nasal polyps were divided into 3 groups by the degree of eosinophilic infiltration. Western blot analysis revealed that HPGDS was more intensely and frequently expressed in the group with high infiltration than in the groups with low or medium infiltration. Hematopoietic prostaglandin D2 synthase was immunohistochemically found in a subpopulation of EG2-positive eosinophils that had accumulated in the nasal polyps but not in the EG2-negative resting eosinophils. The ratio of HPGDS-positive eosinophils to EG2-positive eosinophils in the group with high eosinophil infiltration (mean ± SD, 64.8% ± 19.2%) was twice that in the group with low eosinophil infiltration (30.5% ± 13.8%). Conclusion Prostaglandin D2 was actively produced by an EG2 and HPGDS double-positive subpopulation of activated eosinophils that had infiltrated into nasal polyps. Nasal polyposis is a condition involving chronic airway inflammation of the paranasal sinus mucosa, leading to protrusion of benign edematous polyps from the meatus into the nasal cavities.1 Histologically, nasal polyps typically show the presence of a chronic inflammatory infiltrate with a large number of eosinophils. Patients with asthma, acute recurrent or chronic sinusitis, aspirin-induced asthma, or allergy require more polypectomies and more topical corticosteroid treatments than do patients without these diseases.2 Both secretion eosinophilia and tissue eosinophilia were found most often in patients with aspirin-induced asthma, and these patients had the most active nasal polyposis, as judged by the degree of sinus involvement and number of reoperations and use of medication.3 Prostaglandin D2 (PGD2) is the major prostanoid produced at sites of inflammation and infection4,5 and has an important role in the inflammatory response.6-9 Hematopoietic PGD2 synthase (HPGDS)10-12 contributes to the production of PGD2 in antigen-presenting cells and mast cells in a variety of tissues13-15 and is involved in the activation and differentiation of mast cells as well as in chemotaxis or prolongation of cell survival of eosinophils. In an asthmatic model of knockout mice for D prostanoid 1, a receptor for PGD2, the infiltration of eosinophils was substantially reduced.16 In addition, PGD2 prolongs eosinophil survival by suppressing eosinophil apoptosis through the DP receptor.17,18 However, to our knowledge, no previous study has focused on the relationship between PGD2 production and eosinophil accumulation in nasal polyps. We investigated the expression and cellular localization of HPGDS in nasal polyps with high and low degrees of eosinophil infiltration and found that HPGDS was localized in a subpopulation of EG2-positive (activated) eosinophils in nasal polyposis. Our findings indicate that PGD2 is actively produced by EG2 and HPGDS double-positive activated eosinophils and suggest that the production of PGD2 likely contributes to the recurrence of nasal polyposis. Methods Antibodies Polyclonal rabbit antibodies against human cyclooxygenase (COX)–1, HPGDS, and lipocalin-type PGD synthase and monoclonal mouse anti-human COX-2 antibody were obtained from a commercial supplier (Cayman Chemical Co, Ann Arbor, Michigan). Monoclonal mouse antibodies against human eosinophil major basic protein (MBP) (clone BMK13; Biodesign International, Saco, Maine), eosinophil cationic protein (clone EG2; Pharmacia, Uppsala, Sweden), mast cell tryptase (Chemicon International, Temecula, California), CD68 (DAKO Corp, Carpenteria, California), avidin-biotin-peroxidase complex kit, 3,3′5,5′-tetramethylbenzidine peroxidase substrate kit, and normal rabbit and mouse immunoglobulins (all from Vector Laboratories Inc, Burlingame, California) were purchased from the manufacturers. Tissue handling Nasal polyps were obtained in 19 patients with chronic sinusitis undergoing endoscopic polypectomy. Informed consent was obtained from all patients. Patients were excluded from the study if they had taken systemic corticosteroid or nasal corticosteroid agents during the month before the study. Each nasal polyp was divided in half. One specimen was snap-frozen in liquid nitrogen and kept at −80°C and the other was fixed in a 10% neutral formaldehyde solution and embedded in paraffin. The paraffin-embedded blocks were then cut into 4-μm-thick consecutive sections. Immunohistochemical analysis Paraffin sections were incubated for 1 hour with 10% goat serum to mask the nonspecific binding sites and then at 4°C overnight with antibodies against COX-1 (1:1000), lipocalin-type PGD synthase (1:5000), HPGDS (1:10000), COX-2 (1:1000), EG2 (1:1000), MBP (1:100), mast cell tryptase (1:1000), or CD68 (ready-to-use solution). The sections were then reacted with biotinylated secondary antibodies against rabbit and mouse IgG. Thereafter, they were incubated for 30 minutes with the avidin-biotin-peroxidase complex kit and the signal was visualized with diaminobenzidine tetrahydrochloride as a chromogen. Negative controls consisted of normal rabbit or mouse immunoglobulin or the antibody absorbed with an excess amount of the recombinant HPGDS. In double staining, MBP or CD68 was immunostained in brown with diaminobenzidine tetrahydrochloride and EG2 or HPGDS, and in blue with 3,3′5,5′-tetramethylbenzidine. For double immunofluorescence staining, the slides were incubated with rabbit antibody against HPGDS and mouse antibody against mast cell tryptase, MBP, EG2, or CD68 and then with Alexa Fluor 488–labeled anti-rabbit IgG and Alexa Fluor 546–labeled anti-mouse IgG antibodies (diluted 1:500; Molecular Probes, Invitrogen Corp, Carlsbad, California). Red and green fluorescences were observed with a confocal fluorescence microscope (Radiance 2000; Bio-Rad Laboratories Inc, Hercules, California). Western blot analysis Nasal polyps were homogenized in phosphate-buffered saline solution (1 mL/100 mg wet weight of tissues). After centrifugation of the homogenates at 100 000g at 4°C for 1 hour, proteins in the resultant supernatant were separated by sodium dodecylsulfate–polyacrylamide gel electrophoresis in a 10%:20% gradient gel, and microsomal proteins in a 4%:20% gel. Proteins were transferred onto polyvinyl difluoride membranes (Immobilon; Millipore Corp, Bedford, Massachusetts) electrophoretically at 100 mA for 1 hour. After blockage of nonspecific binding sites for 1 hour at 25°C with phosphate-buffered saline solution containing 5% skim milk and 0.1% polysorbate 20 (Tween 20; Wako Junyaku, Osaka, Japan), the membranes were incubated at 4°C overnight with antibodies against human COX-1, HPGDS, lipocalin-type PGD synthase (1:5000), or COX-2 (1:1000) followed by horseradish peroxidase–coupled antibodies against mouse or rabbit IgG (1 mg/mL; Jackson ImmunoResearch Laboratories Inc, West Grove, Pennsylvania). The blot was then incubated with an electrochemiluminescence detection reagent (Amersham International PLC, Buckinghamshire, England) and subsequently exposed to an autoradiographic film (Kodak XOMAT AR film; Eastman Kodak Co, Rochester, New York). Statistical analysis Data comparison within different groups was performed with the Kruskal-Wallis test. The significance of differences between 2 groups was calculated using the Mann-Whitney test for unpaired data. P < .05 was considered statistically significant. Results Patient characteristics Clinical characteristics of the 19 patients are given in the Table. Patients were divided into 3 groups, as follows: low eosinophilic infiltration group, characterized by eosinophil infiltration representing less than 10% of the total inflammatory cell infiltrate in the polyp; medium eosinophilic infiltration group, in which eosinophils composed 10% to 20% of the total infiltrate; and high eosinophilic infiltration group, in which eosinophils constituted more than 20% of the total inflammatory cells. There were no significant differences between the 3 groups for age, sex, or prevalence of allergic rhinitis. Although the percentage of peripheral blood eosinophils was statistically the same in low and high eosinophilic infiltration groups, the number of eosinophils in the polyps increased from (mean ± SD) 57.3 ± 48.3/mm2 in the low eosinophilic infiltration group to 775 ± 393/mm2 in the high eosinophilic infiltration group, indicating that eosinophilic accumulation is tissue-specific. Expression of hpgds in nasal polyps with high and low eosinophilic infiltration Western blot analysis revealed that the HPGDS immunoreactive protein was expressed in all samples (n = 7 for each group) of nasal polyps (Figure 1). The intensity of the HPGDS-positive band was weak for 3 samples (L2, L3, and L4) and strong for 2 samples (L6 and L7) in the low eosinophilic infiltration group and for 6 samples (H2 to H7) in the high eosinophilic infiltration group, indicating that HPGDS was more frequently and intensely expressed in polyps with high infiltration compared with polyps with low infiltration. For optical density values obtained by densitometric analysis, the density in the high eosinophilic infiltration group was higher than in the low eosinophilic infiltration group; however, there was no statistical difference between the groups. COX-2 expression was high in 2 samples (L4 and H4) and was not detected in 4 samples (L6, H2, H3, and H5). COX-1 immunoreactivity was observed in all samples. There were no significant differences in expression of COX-1 and COX-2 between the 2 groups. Therefore, expression of HPGDS was characteristic of nasal polyps with high eosinophilic infiltration, yet not specific to them because HPGDS was often observed in polyps with low eosinophilic infiltration. Immunohistochemical localization of hpgds in inflammatory cells of nasal polyps All samples were examined by immunohistochemical staining with anti-HPGDS antibody and antibodies against several marker proteins for eosinophils (MBP and EG2), monocytes (CD68), and mast cells (tryptase). Figure 2 shows typical results of hematoxylin-eosin staining and immunoperoxidase staining for MBP, EG2, CD68, and tryptase, and HPGDS in nasal polyps in the high and low eosinophilic infiltration groups. Results of confocal double-immunofluorescence staining of polyps with low and high eosinophilic infiltration with anti-CD68 or anti–mast cell tryptase antibody and anti-HPGDS antibody are shown in Figure 3, and with anti-MBP or EG2 antibody and anti-HPGDS antibody in Figure 4. Hematoxylin-eosin staining revealed that monocytes, plasma cells, lymphocytes, and a few eosinophils had infiltrated into polyps with low eosinophilic infiltration (Figure 2A). In contrast, eosinophils were the dominant cells in the infiltrate in polyps with high eosinophilic infiltration (Figure 2B). We used 2 recognized eosinophilic markers, MBP and EG2, to differentiate resting from activated eosinophils. Anti-MBP antibody recognizes both resting and activated eosinophils, whereas EG2 antibody reacts selectively with activated eosinophils. In polyps with low eosinophilic infiltration (eg, L1), eosinophils stained positive with the anti-MBP antibody (brown in Figure 2C) but scarcely with the EG2 antibody (blue in Figure 2C), indicating that most of the eosinophils that had infiltrated into the polyp had not been activated. Approximately 60% of the MBP-immunoreactive eosinophils in polyps with high eosinophilic infiltration (eg, H3) stained positive with the EG2 antibody (Figure 2D), indicating that most of them were active. As can be seen in the Table, the percentage of activated eosinophils in the polyps, expressed by the ratio of EG2-positive cells to MBP-positive cells, varied from 0.7% to 90% in polyps with low eosinophilic infiltration and from 14% to 99% in polyps with high eosinophilic infiltration. The mean (± SD) ratio was not statistically different between the 2 groups (46.8% ± 29.2% and 65.8% ± 34.7%, respectively). There were no significant differences in the number of cells positive for mast cell tryptase or CD68 between the 2 groups (Figure 2E-H). In polyps with low eosinophilic infiltration (Figure 2I), HPGDS immunoreactivity was found in monocytes, mast cells, and eosinophils, in equal proportions. The HPGDS-positive monocytes were colabeled with anti-CD68 antibody (Figure 3A), the HPGDS-positive mast cells with antitryptase antibody (Figure 3B), and HPGDS-positive eosinophils with anti-MBP antibody (Figure 4A). The HPGDS immunoreactivity was not detected in a subpopulation of MBP-positive or EG2-positive eosinophils (Figure 4A and B). In the high eosinophilic infiltration group (Figure 2J), HPGDS immunoreactivity was found in a large number of eosinophils, most of which were colabeled with anti-MBP antibody (Figure 4C) or EG2 antibody (Figure 4D). The EG2-negative eosinophils were rarely labeled with anti-HPGDS antibody in either group, indicating that HPGDS expression was a marker of activated eosinophils. Hpgds expression in a subpopulation of eg2-positive activated eosinophils in nasal polyps The Table also gives the percentages of eosinophils simultaneously labeled with antibodies against either of the 2 eosinophilic markers MBP and EG2, and the anti-HPGDS antibody in all samples. The ratio of HPGDS and MBP double-positive cells to MBP-positive eosinophils was relatively low in the group with low eosinophilic infiltration (12.1% ± 13.3%) but was 3.5-fold higher in the group with high eosinophilic infiltration (43.8% ± 26.0%). The ratio of HPGDS-positive cells to EG2-positive eosinophils in the group with high infiltration (64.8% ± 19.2%) was twice that in the group with low infiltration (30.5% ± 13.8%). In both cases, the differences in these ratios between the 2 groups of patients was statistically significant (P < .002). Our results show that HPGDS was not expressed in resting eosinophils (MBP-positive and EG2-negative cells) in the peripheral blood (data not shown) or in polyps. The HPGDS was expressed specifically in about 30% and 60% of the EG2-positive (activated) eosinophils in the groups with low and high eosinophilic infiltration, respectively. The percentage of EG2 and HPGDS double-positive cells in eosinophils was relatively higher in the group with high vs low eosinophilic infiltration; the high eosinophilic infiltration group had more active nasal polyposis. Together these results suggest that HPGDS was expressed in more activated eosinophils than EG2-positive eosinophils in nasal polyps and contributes to tissue-specific eosinophilia and the recurrence of nasal polyps. Comment To our knowledge, this is the first study to find that HPGDS was expressed in a subpopulation of EG2-positive (activated) eosinophils that had infiltrated into human nasal polyps. We found no previous report of the localization of HPGDS in eosinophils, although HPGDS was previously found in antigen-presenting cells, mast cells, and megakaryocytes in the peripheral tissue7,19-21 and in helper T cells in the peripheral blood.22 Nantel et al21 in 2004 reported that HPGDS was not detected in eosinophils in human nasal polyps. We also found that HPGDS was not expressed in MBP-positive but EG2-negative eosinophils, which were dominant in most of the samples with low eosinophilic infiltration. For example, in sample L1 with low infiltration of a polyp, many eosinophils accumulated in the polyp (140 cells/mm2) but the percentage of HPGDS-positive eosinophils was low (0.4%); thus, HPGDS-negative eosinophils were dominant in this case. It would seem that Nantel and colleagues examined the low infiltration polyps rich in preactivated EG2-negative eosinophils. However, even in the low infiltration group, samples L6 and L7 with slight and mild eosinophilic infiltration (5 and 40 cells/mm2, respectively) showed strong expression of HPGDS-immunoreactive protein, as determined at Western blot analysis, and a high percentage of HPGDS-positive activated eosinophils (20% and 38%, respectively) that had infiltrated into the polyp. Commonly, 8% to 70% of MBP-positive eosinophils were positive for HPGDS. The percentage of HPGDS-positive cells in EG2-positive (activated) eosinophils also was higher, being twice that in polyps with high vs low infiltration. These results suggest that HPGDS is not only a marker of eosinophilic inflammation but also a sign of activation of infiltrating eosinophils. Prostaglandin D2 exerts its actions by binding to 2 types of receptors: DP (DP1) and CRTH2 (chemoattractant receptor–homologous molecule expressed on Th2 [DP2]). Both of these receptors are expressed on eosinophils. We also detected DP messenger RNA (mRNA) in the nasal polyps, the level of which was slightly higher than that of CRTH2 mRNA (data not shown). The level of HPGDS mRNA was significantly correlated with that of DP mRNA but not with that of CRTH2 mRNA (data not shown). Prostaglandin D2 induces chemotaxis of eosinophils, basophils, and Th2 cells that is CRTH2-mediated.17,23 Stimulation of DP delays the onset of apoptosis of cultured eosinophils.17,18 Our findings, together with previous observations, suggest that the local production of PGD2 by HPGDS-positive activated eosinophils is likely of great importance for further infiltration of eosinophils and more prolonged survival of tissue eosinophils in nasal polyps. The results of this study indicate that HPGDS is expressed in a subpopulation of activated eosinophils that accumulate in nasal polyps. Furthermore, our data suggest that PGD2 produced by HPGDS-positive activated eosinophils may be an important prognostic factor for the clinical course of nasal polyposis. Back to top Article Information Correspondence: Sawaka Hyo, MD, Department of Otorhinolaryngology, Osaka Medical College, Daigaku-cho, Takatsuki City, Osaka 569, Japan (oto039@poh.osaka-med.ac.jp). Submitted for Publication: March 30, 2006; final revision received September 9, 2006; accepted September 28, 2006. Author Contributions: Dr Hyo had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Hyo, Kawata, Kadoyama, Eguchi, Kubota, Takenaka, and Urade. Acquisition of data: Hyo. Analysis and interpretation of data: Hyo, Kawata, and Urade. Drafting of the manuscript: Hyo and Eguchi. Critical revision of the manuscript for important intellectual content: Hyo, Kawata, Kadoyama, Kubota, Takenaka, and Urade. Statistical analysis: Hyo, Kawata, and Eguchi. Obtained funding: Hyo, Kawata, Kadoyama, and Urade. Administrative, technical, and material support: Kawata, Kadoyama, Kubota, and Urade. Study supervision: Kubota, Takenaka, and Urade. Financial Disclosure: None reported. Funding/Support: This study was supported by the Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation, by a research grant from the Japan Foundation for Applied Enzymology, and by TAIHO Pharmaceutical Co Ltd. Role of the Sponsor: TAIHO Pharmaceutical Co Ltd had no role in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript. Additional Contributions: Mss Shigeko Matsumoto and Nanae Nagata provided expert technical support, and Michitoshi Araki, MD, and Yasuhito Hattori, MD, provided advice on the clinical data. References 1. Mygind N Nasal polyposis. J Allergy Clin Immunol 1990;86 (6, pt 1) 827- 829PubMedGoogle ScholarCrossref 2. Larsen KTos M Clinical course of patients with primary nasal polyps. Acta Otolaryngol 1994;114 (5) 556- 559PubMedGoogle ScholarCrossref 3. Meltzer EOHamilos DLHadley JA et al. Rhinosinusitis: establishing definitions for clinical research and patient care. J Allergy Clin Immunol 2004;114(6 suppl)155- 212PubMedGoogle ScholarCrossref 4. Ajuebor MNSingh AWallace JL Cyclooxygenase-2-derived prostaglandin D2 is an early anti-inflammatory signal in experimental colitis. Am J Physiol Gastrointest Liver Physiol 2000;279 (1) G238- G244PubMedGoogle Scholar 5. Gilroy DWColville-Nash PRWillis DChivers JPaul-Clark MJWilloughby DA Inducible cyclooxygenase may have anti-inflammatory properties. Nat Med 1999;5 (6) 698- 701PubMedGoogle ScholarCrossref 6. Roberts LJ IISweetman BJLewis RAAusten KFOates JA Increased production of prostaglandin D2 in patients with systemic mastocytosis. N Engl J Med 1980;303 (24) 1400- 1404PubMedGoogle ScholarCrossref 7. Urade YHayaishi O Prostaglandin D synthase: structure and function. Vitam Horm 2000;5889- 120PubMedGoogle Scholar 8. Murakami MMatsumoto RUrade YAusten KFArm JP c-kit Ligand mediates increased expression of cytosolic phospholipase A2, prostaglandin endoperoxide synthase-1, and hematopoietic prostaglandin D2 synthase and increased IgE-dependent prostaglandin D2 generation in immature mouse mast cells. J Biol Chem 1995;270 (7) 3239- 3246PubMedGoogle ScholarCrossref 9. Angeli VFaveeuw CRoye O et al. Role of the parasite-derived prostaglandin D2 in the inhibition of epidermal Langerhans cell migration during schistosomiasis infection. J Exp Med 2001;193 (10) 1135- 1147PubMedGoogle ScholarCrossref 10. Christ-Hazelhof ENugteren DH Purification and characterisation of prostaglandin endoperoxide D-isomerase, a cytoplasmic, glutathione-requiring enzyme. Biochim Biophys Acta 1979;572 (1) 43- 51PubMedGoogle ScholarCrossref 11. Urade YFujimoto NUjihara MHayaishi O Biochemical and immunological characterization of rat spleen prostaglandin D synthetase. J Biol Chem 1987;262 (8) 3820- 3825PubMedGoogle Scholar 12. Urade YMohri IAritake KInoue TMiyano M Biochemical and structural characteristics of hematopoietic prostaglandin D synthase: from evolutional analysis to drug designing. In: Morikawa K, Tate S, eds. Functional and Structural Biology on the Lipo-Network. Karala, India: Transworld Research Network; in press 13. Ujihara MHoriguchi YIkai KUrade Y Characterization and distribution of prostaglandin D synthetase in rat skin. J Invest Dermatol 1988;90 (4) 448- 451PubMedGoogle ScholarCrossref 14. Urade YUjihara MHoriguchi Y et al. Mast cells contain spleen-type prostaglandin D synthase. J Biol Chem 1990;265 (1) 371- 375PubMedGoogle Scholar 15. Urade YUjihara MHoriguchi YIkai KHayaishi O The major source of endogenous prostaglandin D2 production is likely antigen-presenting cells: localization of glutathione-requiring prostaglandin D synthase in histiocytes, dendritic and Kupffer cells in various rat tissues. J Immunol 1989;143 (9) 2982- 2989PubMedGoogle Scholar 16. Matsuoka THirata MTanaka H et al. Prostaglandin D2 as a mediator of allergic asthma. Science 2000;287 (5460) 2013- 2017PubMedGoogle ScholarCrossref 17. Gervais FGCruz RPChateauneuf A et al. Selective modulation of chemokinesis, degranulation, and apoptosis in eosinophils through the PGD2 receptors CRTH2 and DP. J Allergy Clin Immunol 2001;108 (6) 982- 988PubMedGoogle ScholarCrossref 18. Monneret GGravel SDiamond MRokach JPowell WS Prostaglandin D2 is a potent chemoattractant for human eosinophils that acts via a novel DP receptor. Blood 2001;98 (6) 1942- 1948PubMedGoogle ScholarCrossref 19. Fujimori KKanaoka YSakaguchi YUrade Y Transcriptional activation of the human hematopoietic prostaglandin D synthase gene in megakaryoblastic cells: role of the oct-1 element in the 5′-flanking region and the AP-2 element in the untranslated exon-1. J Biol Chem 2000;275 (51) 40511- 40516PubMedGoogle ScholarCrossref 20. Kanaoka YAgo HInagaki E et al Cloning and crystal structure of hematopoietic prostaglandin D synthase. Cell199790610851095 [published correction appears in Cell. 1999;96(3):449] PubMedGoogle Scholar 21. Nantel FFong CLamontague S et al. Expression of prostaglandin D2 receptors DP and CRTH2 in human nasal mucosa. Prostaglandins Other Lipid Mediat 2004;73 (1-2) 87- 101PubMedGoogle ScholarCrossref 22. Tanaka KOgawa KSugamura KNakamura MTakano SNagata K Cutting edge: differential production of prostaglandin D2 by human helper T cell subset. J Immunol 2000;164 (5) 2277- 2280PubMedGoogle ScholarCrossref 23. Hirai HTanaka KYoshie O et al. Prostaglandin D2 selectively induces chemotaxis in T helper type 2 cells, eosinophils and basophils via seven-transmembrane receptor CRTH2. J Exp Med 2001;193 (2) 255- 261PubMedGoogle ScholarCrossref http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Archives of Otolaryngology–Head & Neck Surgery American Medical Association

Expression of Prostaglandin D2 Synthase in Activated Eosinophils in Nasal Polyps

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American Medical Association
Copyright
Copyright © 2007 American Medical Association. All Rights Reserved.
ISSN
0886-4470
DOI
10.1001/archotol.133.7.693
pmid
17638783
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Abstract

Abstract Objective To clarify the relationship between prostaglandin D2 production and eosinophil accumulation. Design Screening and diagnostic tests. Subjects Nineteen patients with chronic rhinosinusitis. Interventions Nasal polyps were obtained from 19 patients at endoscopic sinus surgery. Eosinophils in nasal polyps were counted after hematoxylin-eosin staining and immunostaining with antibodies against 2 eosinophil markers—major basic protein and EG2. Hematopoietic prostaglandin D2 synthase (HPGDS) expression was examined by semiquantitative Western blot analysis and by immunohistochemical staining with anti-HPGDS antibody. Results Nasal polyps were divided into 3 groups by the degree of eosinophilic infiltration. Western blot analysis revealed that HPGDS was more intensely and frequently expressed in the group with high infiltration than in the groups with low or medium infiltration. Hematopoietic prostaglandin D2 synthase was immunohistochemically found in a subpopulation of EG2-positive eosinophils that had accumulated in the nasal polyps but not in the EG2-negative resting eosinophils. The ratio of HPGDS-positive eosinophils to EG2-positive eosinophils in the group with high eosinophil infiltration (mean ± SD, 64.8% ± 19.2%) was twice that in the group with low eosinophil infiltration (30.5% ± 13.8%). Conclusion Prostaglandin D2 was actively produced by an EG2 and HPGDS double-positive subpopulation of activated eosinophils that had infiltrated into nasal polyps. Nasal polyposis is a condition involving chronic airway inflammation of the paranasal sinus mucosa, leading to protrusion of benign edematous polyps from the meatus into the nasal cavities.1 Histologically, nasal polyps typically show the presence of a chronic inflammatory infiltrate with a large number of eosinophils. Patients with asthma, acute recurrent or chronic sinusitis, aspirin-induced asthma, or allergy require more polypectomies and more topical corticosteroid treatments than do patients without these diseases.2 Both secretion eosinophilia and tissue eosinophilia were found most often in patients with aspirin-induced asthma, and these patients had the most active nasal polyposis, as judged by the degree of sinus involvement and number of reoperations and use of medication.3 Prostaglandin D2 (PGD2) is the major prostanoid produced at sites of inflammation and infection4,5 and has an important role in the inflammatory response.6-9 Hematopoietic PGD2 synthase (HPGDS)10-12 contributes to the production of PGD2 in antigen-presenting cells and mast cells in a variety of tissues13-15 and is involved in the activation and differentiation of mast cells as well as in chemotaxis or prolongation of cell survival of eosinophils. In an asthmatic model of knockout mice for D prostanoid 1, a receptor for PGD2, the infiltration of eosinophils was substantially reduced.16 In addition, PGD2 prolongs eosinophil survival by suppressing eosinophil apoptosis through the DP receptor.17,18 However, to our knowledge, no previous study has focused on the relationship between PGD2 production and eosinophil accumulation in nasal polyps. We investigated the expression and cellular localization of HPGDS in nasal polyps with high and low degrees of eosinophil infiltration and found that HPGDS was localized in a subpopulation of EG2-positive (activated) eosinophils in nasal polyposis. Our findings indicate that PGD2 is actively produced by EG2 and HPGDS double-positive activated eosinophils and suggest that the production of PGD2 likely contributes to the recurrence of nasal polyposis. Methods Antibodies Polyclonal rabbit antibodies against human cyclooxygenase (COX)–1, HPGDS, and lipocalin-type PGD synthase and monoclonal mouse anti-human COX-2 antibody were obtained from a commercial supplier (Cayman Chemical Co, Ann Arbor, Michigan). Monoclonal mouse antibodies against human eosinophil major basic protein (MBP) (clone BMK13; Biodesign International, Saco, Maine), eosinophil cationic protein (clone EG2; Pharmacia, Uppsala, Sweden), mast cell tryptase (Chemicon International, Temecula, California), CD68 (DAKO Corp, Carpenteria, California), avidin-biotin-peroxidase complex kit, 3,3′5,5′-tetramethylbenzidine peroxidase substrate kit, and normal rabbit and mouse immunoglobulins (all from Vector Laboratories Inc, Burlingame, California) were purchased from the manufacturers. Tissue handling Nasal polyps were obtained in 19 patients with chronic sinusitis undergoing endoscopic polypectomy. Informed consent was obtained from all patients. Patients were excluded from the study if they had taken systemic corticosteroid or nasal corticosteroid agents during the month before the study. Each nasal polyp was divided in half. One specimen was snap-frozen in liquid nitrogen and kept at −80°C and the other was fixed in a 10% neutral formaldehyde solution and embedded in paraffin. The paraffin-embedded blocks were then cut into 4-μm-thick consecutive sections. Immunohistochemical analysis Paraffin sections were incubated for 1 hour with 10% goat serum to mask the nonspecific binding sites and then at 4°C overnight with antibodies against COX-1 (1:1000), lipocalin-type PGD synthase (1:5000), HPGDS (1:10000), COX-2 (1:1000), EG2 (1:1000), MBP (1:100), mast cell tryptase (1:1000), or CD68 (ready-to-use solution). The sections were then reacted with biotinylated secondary antibodies against rabbit and mouse IgG. Thereafter, they were incubated for 30 minutes with the avidin-biotin-peroxidase complex kit and the signal was visualized with diaminobenzidine tetrahydrochloride as a chromogen. Negative controls consisted of normal rabbit or mouse immunoglobulin or the antibody absorbed with an excess amount of the recombinant HPGDS. In double staining, MBP or CD68 was immunostained in brown with diaminobenzidine tetrahydrochloride and EG2 or HPGDS, and in blue with 3,3′5,5′-tetramethylbenzidine. For double immunofluorescence staining, the slides were incubated with rabbit antibody against HPGDS and mouse antibody against mast cell tryptase, MBP, EG2, or CD68 and then with Alexa Fluor 488–labeled anti-rabbit IgG and Alexa Fluor 546–labeled anti-mouse IgG antibodies (diluted 1:500; Molecular Probes, Invitrogen Corp, Carlsbad, California). Red and green fluorescences were observed with a confocal fluorescence microscope (Radiance 2000; Bio-Rad Laboratories Inc, Hercules, California). Western blot analysis Nasal polyps were homogenized in phosphate-buffered saline solution (1 mL/100 mg wet weight of tissues). After centrifugation of the homogenates at 100 000g at 4°C for 1 hour, proteins in the resultant supernatant were separated by sodium dodecylsulfate–polyacrylamide gel electrophoresis in a 10%:20% gradient gel, and microsomal proteins in a 4%:20% gel. Proteins were transferred onto polyvinyl difluoride membranes (Immobilon; Millipore Corp, Bedford, Massachusetts) electrophoretically at 100 mA for 1 hour. After blockage of nonspecific binding sites for 1 hour at 25°C with phosphate-buffered saline solution containing 5% skim milk and 0.1% polysorbate 20 (Tween 20; Wako Junyaku, Osaka, Japan), the membranes were incubated at 4°C overnight with antibodies against human COX-1, HPGDS, lipocalin-type PGD synthase (1:5000), or COX-2 (1:1000) followed by horseradish peroxidase–coupled antibodies against mouse or rabbit IgG (1 mg/mL; Jackson ImmunoResearch Laboratories Inc, West Grove, Pennsylvania). The blot was then incubated with an electrochemiluminescence detection reagent (Amersham International PLC, Buckinghamshire, England) and subsequently exposed to an autoradiographic film (Kodak XOMAT AR film; Eastman Kodak Co, Rochester, New York). Statistical analysis Data comparison within different groups was performed with the Kruskal-Wallis test. The significance of differences between 2 groups was calculated using the Mann-Whitney test for unpaired data. P < .05 was considered statistically significant. Results Patient characteristics Clinical characteristics of the 19 patients are given in the Table. Patients were divided into 3 groups, as follows: low eosinophilic infiltration group, characterized by eosinophil infiltration representing less than 10% of the total inflammatory cell infiltrate in the polyp; medium eosinophilic infiltration group, in which eosinophils composed 10% to 20% of the total infiltrate; and high eosinophilic infiltration group, in which eosinophils constituted more than 20% of the total inflammatory cells. There were no significant differences between the 3 groups for age, sex, or prevalence of allergic rhinitis. Although the percentage of peripheral blood eosinophils was statistically the same in low and high eosinophilic infiltration groups, the number of eosinophils in the polyps increased from (mean ± SD) 57.3 ± 48.3/mm2 in the low eosinophilic infiltration group to 775 ± 393/mm2 in the high eosinophilic infiltration group, indicating that eosinophilic accumulation is tissue-specific. Expression of hpgds in nasal polyps with high and low eosinophilic infiltration Western blot analysis revealed that the HPGDS immunoreactive protein was expressed in all samples (n = 7 for each group) of nasal polyps (Figure 1). The intensity of the HPGDS-positive band was weak for 3 samples (L2, L3, and L4) and strong for 2 samples (L6 and L7) in the low eosinophilic infiltration group and for 6 samples (H2 to H7) in the high eosinophilic infiltration group, indicating that HPGDS was more frequently and intensely expressed in polyps with high infiltration compared with polyps with low infiltration. For optical density values obtained by densitometric analysis, the density in the high eosinophilic infiltration group was higher than in the low eosinophilic infiltration group; however, there was no statistical difference between the groups. COX-2 expression was high in 2 samples (L4 and H4) and was not detected in 4 samples (L6, H2, H3, and H5). COX-1 immunoreactivity was observed in all samples. There were no significant differences in expression of COX-1 and COX-2 between the 2 groups. Therefore, expression of HPGDS was characteristic of nasal polyps with high eosinophilic infiltration, yet not specific to them because HPGDS was often observed in polyps with low eosinophilic infiltration. Immunohistochemical localization of hpgds in inflammatory cells of nasal polyps All samples were examined by immunohistochemical staining with anti-HPGDS antibody and antibodies against several marker proteins for eosinophils (MBP and EG2), monocytes (CD68), and mast cells (tryptase). Figure 2 shows typical results of hematoxylin-eosin staining and immunoperoxidase staining for MBP, EG2, CD68, and tryptase, and HPGDS in nasal polyps in the high and low eosinophilic infiltration groups. Results of confocal double-immunofluorescence staining of polyps with low and high eosinophilic infiltration with anti-CD68 or anti–mast cell tryptase antibody and anti-HPGDS antibody are shown in Figure 3, and with anti-MBP or EG2 antibody and anti-HPGDS antibody in Figure 4. Hematoxylin-eosin staining revealed that monocytes, plasma cells, lymphocytes, and a few eosinophils had infiltrated into polyps with low eosinophilic infiltration (Figure 2A). In contrast, eosinophils were the dominant cells in the infiltrate in polyps with high eosinophilic infiltration (Figure 2B). We used 2 recognized eosinophilic markers, MBP and EG2, to differentiate resting from activated eosinophils. Anti-MBP antibody recognizes both resting and activated eosinophils, whereas EG2 antibody reacts selectively with activated eosinophils. In polyps with low eosinophilic infiltration (eg, L1), eosinophils stained positive with the anti-MBP antibody (brown in Figure 2C) but scarcely with the EG2 antibody (blue in Figure 2C), indicating that most of the eosinophils that had infiltrated into the polyp had not been activated. Approximately 60% of the MBP-immunoreactive eosinophils in polyps with high eosinophilic infiltration (eg, H3) stained positive with the EG2 antibody (Figure 2D), indicating that most of them were active. As can be seen in the Table, the percentage of activated eosinophils in the polyps, expressed by the ratio of EG2-positive cells to MBP-positive cells, varied from 0.7% to 90% in polyps with low eosinophilic infiltration and from 14% to 99% in polyps with high eosinophilic infiltration. The mean (± SD) ratio was not statistically different between the 2 groups (46.8% ± 29.2% and 65.8% ± 34.7%, respectively). There were no significant differences in the number of cells positive for mast cell tryptase or CD68 between the 2 groups (Figure 2E-H). In polyps with low eosinophilic infiltration (Figure 2I), HPGDS immunoreactivity was found in monocytes, mast cells, and eosinophils, in equal proportions. The HPGDS-positive monocytes were colabeled with anti-CD68 antibody (Figure 3A), the HPGDS-positive mast cells with antitryptase antibody (Figure 3B), and HPGDS-positive eosinophils with anti-MBP antibody (Figure 4A). The HPGDS immunoreactivity was not detected in a subpopulation of MBP-positive or EG2-positive eosinophils (Figure 4A and B). In the high eosinophilic infiltration group (Figure 2J), HPGDS immunoreactivity was found in a large number of eosinophils, most of which were colabeled with anti-MBP antibody (Figure 4C) or EG2 antibody (Figure 4D). The EG2-negative eosinophils were rarely labeled with anti-HPGDS antibody in either group, indicating that HPGDS expression was a marker of activated eosinophils. Hpgds expression in a subpopulation of eg2-positive activated eosinophils in nasal polyps The Table also gives the percentages of eosinophils simultaneously labeled with antibodies against either of the 2 eosinophilic markers MBP and EG2, and the anti-HPGDS antibody in all samples. The ratio of HPGDS and MBP double-positive cells to MBP-positive eosinophils was relatively low in the group with low eosinophilic infiltration (12.1% ± 13.3%) but was 3.5-fold higher in the group with high eosinophilic infiltration (43.8% ± 26.0%). The ratio of HPGDS-positive cells to EG2-positive eosinophils in the group with high infiltration (64.8% ± 19.2%) was twice that in the group with low infiltration (30.5% ± 13.8%). In both cases, the differences in these ratios between the 2 groups of patients was statistically significant (P < .002). Our results show that HPGDS was not expressed in resting eosinophils (MBP-positive and EG2-negative cells) in the peripheral blood (data not shown) or in polyps. The HPGDS was expressed specifically in about 30% and 60% of the EG2-positive (activated) eosinophils in the groups with low and high eosinophilic infiltration, respectively. The percentage of EG2 and HPGDS double-positive cells in eosinophils was relatively higher in the group with high vs low eosinophilic infiltration; the high eosinophilic infiltration group had more active nasal polyposis. Together these results suggest that HPGDS was expressed in more activated eosinophils than EG2-positive eosinophils in nasal polyps and contributes to tissue-specific eosinophilia and the recurrence of nasal polyps. Comment To our knowledge, this is the first study to find that HPGDS was expressed in a subpopulation of EG2-positive (activated) eosinophils that had infiltrated into human nasal polyps. We found no previous report of the localization of HPGDS in eosinophils, although HPGDS was previously found in antigen-presenting cells, mast cells, and megakaryocytes in the peripheral tissue7,19-21 and in helper T cells in the peripheral blood.22 Nantel et al21 in 2004 reported that HPGDS was not detected in eosinophils in human nasal polyps. We also found that HPGDS was not expressed in MBP-positive but EG2-negative eosinophils, which were dominant in most of the samples with low eosinophilic infiltration. For example, in sample L1 with low infiltration of a polyp, many eosinophils accumulated in the polyp (140 cells/mm2) but the percentage of HPGDS-positive eosinophils was low (0.4%); thus, HPGDS-negative eosinophils were dominant in this case. It would seem that Nantel and colleagues examined the low infiltration polyps rich in preactivated EG2-negative eosinophils. However, even in the low infiltration group, samples L6 and L7 with slight and mild eosinophilic infiltration (5 and 40 cells/mm2, respectively) showed strong expression of HPGDS-immunoreactive protein, as determined at Western blot analysis, and a high percentage of HPGDS-positive activated eosinophils (20% and 38%, respectively) that had infiltrated into the polyp. Commonly, 8% to 70% of MBP-positive eosinophils were positive for HPGDS. The percentage of HPGDS-positive cells in EG2-positive (activated) eosinophils also was higher, being twice that in polyps with high vs low infiltration. These results suggest that HPGDS is not only a marker of eosinophilic inflammation but also a sign of activation of infiltrating eosinophils. Prostaglandin D2 exerts its actions by binding to 2 types of receptors: DP (DP1) and CRTH2 (chemoattractant receptor–homologous molecule expressed on Th2 [DP2]). Both of these receptors are expressed on eosinophils. We also detected DP messenger RNA (mRNA) in the nasal polyps, the level of which was slightly higher than that of CRTH2 mRNA (data not shown). The level of HPGDS mRNA was significantly correlated with that of DP mRNA but not with that of CRTH2 mRNA (data not shown). Prostaglandin D2 induces chemotaxis of eosinophils, basophils, and Th2 cells that is CRTH2-mediated.17,23 Stimulation of DP delays the onset of apoptosis of cultured eosinophils.17,18 Our findings, together with previous observations, suggest that the local production of PGD2 by HPGDS-positive activated eosinophils is likely of great importance for further infiltration of eosinophils and more prolonged survival of tissue eosinophils in nasal polyps. The results of this study indicate that HPGDS is expressed in a subpopulation of activated eosinophils that accumulate in nasal polyps. Furthermore, our data suggest that PGD2 produced by HPGDS-positive activated eosinophils may be an important prognostic factor for the clinical course of nasal polyposis. Back to top Article Information Correspondence: Sawaka Hyo, MD, Department of Otorhinolaryngology, Osaka Medical College, Daigaku-cho, Takatsuki City, Osaka 569, Japan (oto039@poh.osaka-med.ac.jp). Submitted for Publication: March 30, 2006; final revision received September 9, 2006; accepted September 28, 2006. Author Contributions: Dr Hyo had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Hyo, Kawata, Kadoyama, Eguchi, Kubota, Takenaka, and Urade. Acquisition of data: Hyo. Analysis and interpretation of data: Hyo, Kawata, and Urade. Drafting of the manuscript: Hyo and Eguchi. Critical revision of the manuscript for important intellectual content: Hyo, Kawata, Kadoyama, Kubota, Takenaka, and Urade. Statistical analysis: Hyo, Kawata, and Eguchi. Obtained funding: Hyo, Kawata, Kadoyama, and Urade. Administrative, technical, and material support: Kawata, Kadoyama, Kubota, and Urade. Study supervision: Kubota, Takenaka, and Urade. Financial Disclosure: None reported. Funding/Support: This study was supported by the Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation, by a research grant from the Japan Foundation for Applied Enzymology, and by TAIHO Pharmaceutical Co Ltd. Role of the Sponsor: TAIHO Pharmaceutical Co Ltd had no role in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript. Additional Contributions: Mss Shigeko Matsumoto and Nanae Nagata provided expert technical support, and Michitoshi Araki, MD, and Yasuhito Hattori, MD, provided advice on the clinical data. References 1. Mygind N Nasal polyposis. 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Journal

Archives of Otolaryngology–Head & Neck SurgeryAmerican Medical Association

Published: Jul 1, 2007

References