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1.
Thorax ; 73(8): 758-768, 2018 08.
Article in English | MEDLINE | ID: mdl-29622694

ABSTRACT

BACKGROUND: Respiratory fungal exposure is known to be associated with severe allergic lung inflammation. Airway epithelium is an essential controller of allergic inflammation. An innate immune recognition receptor, nucleotide-binding domain, leucine-rich-containing family, pyrin-domain-containing-3 (NLRP3) inflammasome, and phosphoinositide 3 kinase (PI3K)-δ in airway epithelium are involved in various inflammatory processes. OBJECTIVES: We investigated the role of NLRP3 inflammasome in fungi-induced allergic lung inflammation and examined the regulatory mechanism of NLRP3 inflammasome, focusing on PI3K-δ in airway epithelium. METHODS: We used two in vivo models induced by exposure to Aspergillus fumigatus (Af) and Alternaria alternata (Aa), as well as an Af-exposed in vitro system. We also checked NLRP3 expression in lung tissues from patients with allergic bronchopulmonary aspergillosis (ABPA). RESULTS: Assembly/activation of NLRP3 inflammasome was increased in the lung of Af-exposed mice. Elevation of NLRP3 inflammasome assembly/activation was observed in Af-stimulated murine and human epithelial cells. Similarly, pulmonary expression of NLRP3 in patients with ABPA was increased. Importantly, neutralisation of NLRP3 inflammasome derived IL-1ß alleviated pathophysiological features of Af-induced allergic inflammation. Furthermore, PI3K-δ blockade improved Af-induced allergic inflammation through modulation of NLRP3 inflammasome, especially in epithelial cells. This modulatory role of PI3K-δ was mediated through the regulation of mitochondrial reactive oxygen species (mtROS) generation. NLRP3 inflammasome was also implicated in Aa-induced eosinophilic allergic inflammation, which was improved by PI3K-δ blockade. CONCLUSION: These findings demonstrate that fungi-induced assembly/activation of NLRP3 inflammasome in airway epithelium may be modulated by PI3K-δ, which is mediated partly through the regulation of mtROS generation. Inhibition of PI3K-δ may have potential for treating fungi-induced severe allergic lung inflammation.


Subject(s)
Alternariosis/enzymology , Alternariosis/immunology , Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillosis, Allergic Bronchopulmonary/immunology , Endoplasmic Reticulum Stress/immunology , Immunity, Innate/immunology , Phosphatidylinositol 3-Kinases/immunology , Animals , Aspergillus fumigatus , Biomarkers/analysis , Bronchi/cytology , Cells, Cultured , Epithelial Cells/immunology , Female , Humans , Inflammasomes/immunology , Mice , Mice, Inbred C57BL , Reactive Oxygen Species/immunology
2.
Thorax ; 71(1): 52-63, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26543090

ABSTRACT

BACKGROUND: Sensitisation with Aspergillus fumigatus (Af) is known to be associated with severe allergic lung inflammation, but the mechanism remains to be clarified. Phosphoinositide 3-kinase (PI3K)-δ and endoplasmic reticulum (ER) stress are suggested to be involved in steroid-resistant lung inflammation. We aimed to elucidate the role of PI3K-δ and its relationship with ER stress in fungus-induced allergic lung inflammation. METHODS: Using Af-exposed in vivo and in vitro experimental systems, we examined whether PI3K-δ regulates ER stress, thereby contributing to steroid resistance in fungus-induced allergic lung inflammation. Moreover, we checked expression of an ER stress marker in lung tissues isolated from patients with allergic bronchopulmonary aspergillosis. RESULTS: Af-exposed mice showed that ER stress markers, unfolded protein response (UPR)-related proteins, phosphorylated Akt, generation of mitochondrial reactive oxygen species (mtROS), eosinophilic allergic inflammation, and airway hyperresponsiveness (AHR) were increased in the lung. Similarly, glucose-regulated protein 78 was increased in lung tissues of patients with ABPA. A PI3K-δ inhibitor reduced Af-induced increases in ER stress markers, UPR-related proteins, allergic inflammation and AHR in mice. However, dexamethasone failed to reduce Af-induced allergic inflammation, AHR and elevation of ER stress. Administration of an ER stress inhibitor or a mtROS scavenger improved Af-induced allergic inflammation. The PI3K-δ inhibitor reduced Af-induced mtROS generation and the mtROS scavenger ameliorated ER stress. In primary cultured tracheal epithelial cells, Af-induced ER stress was inhibited by blockade of PI3K-δ. CONCLUSIONS: These findings suggest that PI3K-δ regulates Af-induced steroid-resistant eosinophilic allergic lung inflammation through ER stress.


Subject(s)
Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillosis, Allergic Bronchopulmonary/etiology , Endoplasmic Reticulum Stress/physiology , Phosphatidylinositol 3-Kinases/physiology , Adenine/analogs & derivatives , Adenine/pharmacology , Animals , Biomarkers/analysis , Blotting, Western , Bronchoalveolar Lavage , CCAAT-Enhancer-Binding Proteins/analysis , Female , Glutathione/analysis , Glutathione Disulfide/analysis , Immunoglobulin E/blood , Inflammation/enzymology , Inflammation/etiology , Mice , Mice, Inbred C57BL , Microscopy, Confocal , Quinazolines/pharmacology , RNA, Small Interfering/analysis
3.
J Leukoc Biol ; 87(3): 457-66, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20007243

ABSTRACT

Cumulative evidence indicates that the sialyltransferase ST6Gal-1 and the sialyl-glycans, which it constructs, are functionally pleiotropic. Expression of the ST6Gal-1 gene is mediated by six distinct promoter/regulatory regions, and we hypothesized that these promoters may be used differentially to produce ST6Gal-1 for different biologic purposes. To examine this hypothesis, we compared a mouse with a complete deficiency in ST6Gal-1 (Siat1 null) with another mouse that we have created previously with a disruption only in the P1 promoter (Siat1DeltaP1). We noted previously greater neutrophilic inflammation associated with ST6Gal-1 deficiency. Here, we report that ST6Gal-1-deficient mice also have significantly elevated eosinophilic responses. Upon i.p. thioglycollate elicitation, eosinophils accounted for over 20% of the total peritoneal inflammatory cell pool in ST6Gal-1-deficient animals, which was threefold greater than in corresponding wild-type animals. A principal feature of allergic respiratory inflammation is pulmonary eosinophilia, we evaluated the role of ST6Gal-1 in allergic lung inflammation. Using OVA and ABPA experimental models of allergic airways, we showed that ST6Gal-1 deficiency led to greater airway inflammation characterized by excessive airway eosinophilia. The severity of airway inflammation was similar between Siat1DeltaP1 and Siat1 null mice, indicating a role for P1-generated ST6Gal-1 in regulating eosinophilic inflammation. Colony-forming assays suggested greater IL-5-dependent eosinophil progenitor numbers in the marrow of ST6Gal-1-deficient animals. Moreover, allergen provocation of wild-type mice led to a significant reduction in P1-mediated ST6Gal-1 mRNA and accompanied decline in circulatory ST6Gal-1 levels. Taken together, the data implicate ST6Gal-1 as a participant in regulating not only Th1 but also Th2 responses, and ST6Gal-1 deficiency can lead to the development of more severe allergic inflammation with excessive eosinophil production.


Subject(s)
Eosinophils/immunology , Hypersensitivity/complications , Pneumonia/complications , Pneumonia/enzymology , Promoter Regions, Genetic/genetics , Sialyltransferases/deficiency , Sialyltransferases/genetics , Acute Disease , Animals , Apoptosis , Aspergillosis, Allergic Bronchopulmonary/complications , Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillosis, Allergic Bronchopulmonary/immunology , Aspergillosis, Allergic Bronchopulmonary/pathology , Bronchoalveolar Lavage Fluid/cytology , Cytokines/blood , Disease Models, Animal , Eosinophils/cytology , Eosinophils/enzymology , Hypersensitivity/blood , Hypersensitivity/enzymology , Hypersensitivity/immunology , Immunoglobulin G/blood , Leukocyte Count , Liver/enzymology , Liver/pathology , Longevity , Mice , Peritonitis/chemically induced , Peritonitis/enzymology , Peritonitis/immunology , Pneumonia/blood , Pneumonia/immunology , Sialyltransferases/metabolism , Stem Cells , Th2 Cells/immunology , beta-D-Galactoside alpha 2-6-Sialyltransferase
4.
Clin Exp Allergy ; 37(8): 1239-49, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17651155

ABSTRACT

BACKGROUND: Approximately 20% of the world's asthmatics are suffering from Aspergillus fumigatus (Afu)-induced allergies. The characterization of specific IgE-inducing allergens in allergic aspergillosis patients is fundamental for clinical diagnosis and for immunotherapy. METHODS: Immunoproteomics combined with mass spectrometric analysis was used to identify proteins of third-week culture filtrate (3wcf) potentially responsible for Afu-specific IgE immunoreactivity, using pooled sera from Afu-sensitized asthmatics. Their allergenic potential was also tested against patients with allergic bronchopulmonary aspergillosis (ABPA), by two-dimensional (2-D) gel electrophoresis immunoblotting of 3wcf proteins with individual sera from such patients. This helped us to establish a set of candidate allergens, which could be explored further for diagnostic application in allergic aspergillosis asthmatics including ABPA. RESULTS: Peptide mass fingerprint using matrix-assisted laser desorption/ionization-time of flight-mass spectrometry (MALDI-TOF-MS) and/or de novo sequencing by MS/MS analysis of the protein spots from 2-D gels led to the identification of a total of 16 allergens of Afu. Eleven of them are being reported as allergens for the first time and five had been reported earlier. Putative isoforms of the proteins Asp f 13 and chitosanase have been observed for the first time. When studied for reactivity of these proteins among patients with ABPA using their individual sera, these patients exhibited sensitization although the pattern was varying. Taken together, these proteins could thus be considered as potential allergens even among patients with ABPA. Three of these proteins viz. the hypothetical protein (# spot no. 5), extracellular arabinase (# spot no. 6) and chitosanase (# spot no. 11) could be major allergens with specific IgE immunoreactivity with six out of eight patients' sera. CONCLUSIONS: The immunoproteomic approach applied to the analysis of culture filtrate proteins resulted in the identification of several candidate allergens, many of them novel, contributing to the catalogue of Afu allergenic proteins, which would facilitate improved serodiagnosis for allergic aspergillosis. In addition, the immunoreactivity of these proteins observed among the patients with ABPA may be potentially useful for its serodiagnosis and opens up further opportunities for the development of personalized immunotherapeutics for patients with ABPA.


Subject(s)
Allergens/immunology , Aspergillosis, Allergic Bronchopulmonary/immunology , Aspergillus fumigatus/immunology , Asthma/immunology , Fungal Proteins/immunology , Immunoglobulin E/immunology , Adult , Aspergillosis, Allergic Bronchopulmonary/diagnosis , Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillosis, Allergic Bronchopulmonary/therapy , Aspergillus fumigatus/enzymology , Asthma/diagnosis , Asthma/enzymology , Asthma/therapy , Electrophoresis, Gel, Two-Dimensional , Female , Glycoside Hydrolases/immunology , Humans , Male , Proteomics , Serologic Tests , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
5.
Eur Respir J ; 21(4): 582-8, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12762339

ABSTRACT

Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity reaction to the fungus Aspergillus fumigatus, causing severe asthma that may progress to bronchiectasis. Sputum neutrophilia can occur in association with sputum eosinophilia and correlates with the degree of bronchiectasis. The mechanisms of sputum neutrophilia in ABPA are not known. The aim of this study was to investigate the role of the chemokine interleukin (IL)-8 in sputum neutrophilia in ABPA. Induced sputum was obtained from subjects with ABPA (n=29), and compared to nonsensitised asthma (n=9) and healthy controls (n=21). Semiquantitative polymerase chain reaction was used to assess IL-8 gene expression in induced sputum and IL-8 protein was measured by enzyme-linked immunosorbent assay. Sputum IL-8 protein was significantly higher in ABPA compared to asthma and controls. IL-8 messenger ribonucleic acid/glyceraldehyde-3-phosphate dehydrogenase ratio was elevated in ABPA compared to asthma and controls. Sputum IL-8 correlated with sputum neutrophils, matrix metalloproteinase-9 levels and forced expiratory volume in one second. Interleukin-8 gene expression and protein release were increased in allergic bronchopulmonary aspergillosis and correlated with airway neutrophilia and airway obstruction. The interleukin-8-mediated neutrophil influx in allergic bronchopulmonary aspergillosis may induce lung damage via release of matrix metalloproteinase-9, potentially leading to bronchiectasis.


Subject(s)
Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillosis, Allergic Bronchopulmonary/immunology , Aspergillus fumigatus , Asthma/immunology , Interleukin-8/genetics , Matrix Metalloproteinase 9/metabolism , Neutrophils/immunology , Sputum/immunology , Adult , Analysis of Variance , Aspergillosis, Allergic Bronchopulmonary/diagnostic imaging , Aspergillus fumigatus/immunology , Case-Control Studies , Chi-Square Distribution , Enzyme-Linked Immunosorbent Assay , Eosinophils/immunology , Female , Gene Expression , Humans , Interleukin-8/metabolism , Male , Middle Aged , Polymerase Chain Reaction , Respiratory Function Tests , Tomography, X-Ray Computed
6.
Allergy ; 52(12): 1215-21, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9450141

ABSTRACT

The effect of multiple divided doses compared with single-dose injections of antibodies to murine interleukin (IL)-4 and IL-5 in their respective downregulation of IgE and eosinophilia developing in a model of allergic aspergillosis is investigated. BALB/c mice were exposed to Aspergillus fumigatus antigens (Af) before and along with anticytokine antibodies. The kinetics of blood eosinophils, eosinophil peroxidase (EPO) in bone-marrow cells, serum levels of IgE and Af-specific antibodies, Af-induced cytokine production and mRNA, and lung histology were studied. The results indicate that only multiple anti-IL-5 antibodies were effective in maintaining baseline levels of blood eosinophils. Multiple anti-IL-4 antibodies also downregulated eosinophils in the bone marrow, lung, and peripheral blood, although to a lesser extent than in anti-IL-5 antibody-injected mice. Significant correlation between the EPO activity and the eosinophil numbers in anticytokine antibody-treated mice was observed. The different anti-IL-4 antibody treatments downregulated IgE to the same extent. We conclude that multiple divided doses of anti-IL-5 antibodies are required to sustain normal eosinophil levels in murine allergic aspergillosis. This information may be significant in the therapy of pulmonary allergic diseases.


Subject(s)
Antibodies, Monoclonal/pharmacology , Aspergillosis, Allergic Bronchopulmonary/immunology , Down-Regulation , Eosinophilia/immunology , Immunoglobulin E/blood , Interleukin-4/immunology , Interleukin-5/immunology , Animals , Antibodies, Fungal/analysis , Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillosis, Allergic Bronchopulmonary/pathology , Aspergillus fumigatus/genetics , Aspergillus fumigatus/immunology , Bone Marrow/enzymology , Eosinophil Peroxidase , Eosinophils/enzymology , Eosinophils/pathology , Immunoglobulin G/blood , Leukocyte Count , Lung/pathology , Mice , Mice, Inbred BALB C , Peroxidases/analysis , RNA, Messenger/analysis , Spleen/chemistry
7.
Infect Immun ; 61(5): 1650-6, 1993 May.
Article in English | MEDLINE | ID: mdl-8478053

ABSTRACT

Little is known of the pathophysiology of invasive pulmonary aspergillosis (IPA), an opportunistic fungal infection usually caused by Aspergillus fumigatus. It has been suggested that the ability of the fungus to degrade elastin may aid its invasion and growth in lung tissue. We have described previously the construction of a strain of A. fumigatus in which the gene encoding an alkaline protease, AFAlp, had been disrupted (C.M. Tang, J. Cohen, and D.W. Holden, Mol. Microbiol. 6:1663-1671, 1992); this mutant is deficient in extracellular proteolytic and elastinolytic activity over a broad pH range. In this study, we compared the pathogenicity of this and another AFAlp disruptant with their isogenic, elastase-producing parental strains in two murine models of IPA. In both models, animals were inoculated via the respiratory tract. In the first model, the inoculum was delivered as airborne conidia and animals developed signs of respiratory distress within 2 to 4 days. In the second model, conidia were administered intranasally as a suspension and the disease developed over a 2-week period. No difference was observed between the wild-type and AFAlp disruptants in terms of mortality, and elastin breakdown was detected in lung tissue from animals inoculated with all four strains. We conclude that AFAlp is not a virulence determinant in these models of IPA.


Subject(s)
Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillus fumigatus/pathogenicity , Endopeptidases/metabolism , Serine Endopeptidases/metabolism , Animals , Aspergillosis, Allergic Bronchopulmonary/microbiology , Aspergillosis, Allergic Bronchopulmonary/pathology , Aspergillus fumigatus/enzymology , Base Sequence , Elastin/metabolism , Endopeptidases/genetics , Male , Mice , Mice, Inbred Strains , Molecular Sequence Data , Mutagenesis, Insertional , Oligodeoxyribonucleotides/chemistry , Polymerase Chain Reaction , Serine Endopeptidases/genetics
8.
Can J Microbiol ; 36(1): 33-41, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2185869

ABSTRACT

Two fractions exhibiting acid protease activity (AFPI and AFPII) were isolated by extraction of membrane vesicles of Aspergillus fumigatus with Triton X-100. These two fractions produced single bands in both polyacrylamide and sodium dodecyl sulfate polyacrylamide gel electrophoresis and showed apparent molecular weights of 73,000 and 43,000, respectively. Molecular weights determined by gel filtration in the absence and presence of Triton X-100 and sedimentation velocities in analytical ultracentrifugation indicated hydrophobic characteristics, since both fractions readily aggregated and complexed with Triton X-100; both exhibited elevated enzyme activities in the presence of Triton X-100. Carbohydrate content was 93% for AFPI and 85% for AFPII. The enzymatic fractions demonstrated different pH optima in the acid range as well as different temperature stabilities. Both protease fractions cross reacted in double immunodiffusion, while in crossed immunoelectrophoresis both demonstrated five precipitin peaks, each with similar patterns. AFPI demonstrated two additional precipitin peaks in crossed immunoelectrophoresis. As determined by crossed immunoaffinoelectrophoresis, the protease fractions demonstrated galactose and mannose residues. In biotin-avidin enzyme-linked immunosorbent assay both fractions reacted with allergic bronchopulmonary aspergillosis and aspergilloma sera. It can be concluded that two fractions with protease activity of A. fumigatus reported here may be of significance in Aspergillus-induced diseases.


Subject(s)
Aspergillosis, Allergic Bronchopulmonary/enzymology , Aspergillus fumigatus/enzymology , Peptide Hydrolases/metabolism , Aspergillus fumigatus/immunology , Cell Membrane/enzymology , Humans , Hydrogen-Ion Concentration , Immunoelectrophoresis, Two-Dimensional , Lipids/isolation & purification , Molecular Weight , Peptide Hydrolases/immunology , Temperature
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