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Publication Date
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Author
- Aronica, Mark A2
- Abe, Takuya1
- Aki, Tsunehiro1
- Asaoku, Yoshiko1
- Baba, Koji1
- Bahmed, Karim1
- Beshr Al-Azhary, Diaa1
- Blackburn, Michael R1
- Buffa, Jennifer1
- Cali, Valbona1
- Castillo, Eliseo F1
- Chang, Sarah1
- Chapman, Martin D1
- Comhair, Suzy A1
- Dasgupta, Angira1
- Deering-Rice, Cassandra E1
- Di, Caixia1
- DiDonato, Joseph A1
- Downs, Diana M1
- Dweik, Raed A1
- ElRamlawy, Kareem Gamal1
- Erzurum, Serpil C1
- Fassl, Bernhard1
- Fujimura, Takashi1
- Garantziotis, Stavros1
Keyword
- inflammation5
- allergen3
- lung3
- allergy2
- epitope mapping2
- immunoglobulin E (IgE)2
- immunotherapy2
- T helper cells2
- airway hyperresponsiveness1
- airway remodeling1
- antigenic determinant1
- aspartic protease1
- Aspergillus1
- Basophils1
- Bla g 21
- cell signaling1
- cockroach allergy1
- cytokine1
- OX40-OX40L1
- Rid/YjgF/YER057c/UK114 family1
- Th2 immune responses1
- Th2 response1
- TSG-61
- Western blot1
Molecular Bases of Disease
10 Results
- Molecular Bases of DiseaseOpen Access
MicroRNA-98 reduces nerve growth factor expression in nicotine-induced airway remodeling
Journal of Biological ChemistryVol. 295Issue 52p18051–18064Published online: October 20, 2020- Cherry Wongtrakool
- Junsuk Ko
- Andrew J. Jang
- Kora Grooms
- Sarah Chang
- Cory Sylber
- and others
Cited in Scopus: 5Evolving evidence suggests that nicotine may contribute to impaired asthma control by stimulating expression of nerve growth factor (NGF), a neurotrophin associated with airway remodeling and airway hyperresponsiveness. We explored the hypothesis that nicotine increases NGF by reducing lung fibroblast (LF) microRNA-98 (miR-98) and PPARγ levels, thus promoting airway remodeling. Levels of NGF, miR-98, PPARγ, fibronectin 1 (FN1), endothelin-1 (EDN1, herein referred to as ET-1), and collagen (COL1A1 and COL3A1) were measured in human LFs isolated from smoking donors, in mouse primary LFs exposed to nicotine (50 μg/ml), and in whole lung homogenates from mice chronically exposed to nicotine (100 μg/ml) in the drinking water. - ArticleOpen Access
Heat shock protein 70 is a positive regulator of airway inflammation and goblet cell hyperplasia in a mouse model of allergic airway inflammation
Journal of Biological ChemistryVol. 294Issue 41p15082–15094Published online: August 20, 2019- Dan J.K. Yombo
- Margaret M. Mentink-Kane
- Mark S. Wilson
- Thomas A. Wynn
- Satish K. Madala
Cited in Scopus: 12Heat shock proteins (Hsps) are highly conserved molecular chaperones that are ubiquitously expressed in all species to aid the solubilization of misfolded proteins, protein degradation, and transport. Elevated levels of Hsp70 have been found in the sputum, serum, and bronchoalveolar lavage (BAL) fluid of asthma patients and are known to correlate with disease severity. However, the function of Hsp70 in allergic airway inflammation has remained largely unknown. This study aimed to determine the role of Hsp70 in airway inflammation and remodeling using a mouse model of allergic airway inflammation. - Glycobiology and Extracellular MatricesOpen Access
TNF-stimulated gene 6 promotes formation of hyaluronan–inter-α-inhibitor heavy chain complexes necessary for ozone-induced airway hyperresponsiveness
Journal of Biological ChemistryVol. 292Issue 51p20845–20858Published online: November 9, 2017- Vandy P. Stober
- Collin G. Johnson
- Alana Majors
- Mark E. Lauer
- Valbona Cali
- Ronald J. Midura
- and others
Cited in Scopus: 20Exposure to pollutants, such as ozone, exacerbates airway inflammation and hyperresponsiveness (AHR). TNF-stimulated gene 6 (TSG-6) is required to transfer inter-α-inhibitor heavy chains (HC) to hyaluronan (HA), facilitating HA receptor binding. TSG-6 is necessary for AHR in allergic asthma, because it facilitates the development of a pathological HA–HC matrix. However, the role of TSG-6 in acute airway inflammation is not well understood. Here, we hypothesized that TSG-6 is essential for the development of HA- and ozone-induced AHR. - Molecular Bases of DiseaseOpen Access
Characterization of Transient Receptor Potential Vanilloid-1 (TRPV1) Variant Activation by Coal Fly Ash Particles and Associations with Altered Transient Receptor Potential Ankyrin-1 (TRPA1) Expression and Asthma
Journal of Biological ChemistryVol. 291Issue 48p24866–24879Published online: October 7, 2016- Cassandra E. Deering-Rice
- Chris Stockmann
- Erin G. Romero
- Zhenyu Lu
- Darien Shapiro
- Bryan L. Stone
- and others
Cited in Scopus: 26Transient receptor potential (TRP) channels are activated by environmental particulate materials. We hypothesized that polymorphic variants of transient receptor potential vanilloid-1 (TRPV1) would be uniquely responsive to insoluble coal fly ash compared with the prototypical soluble agonist capsaicin. Furthermore, these changes would manifest as differences in lung cell responses to these agonists and perhaps correlate with changes in asthma symptom control. The TRPV1-I315M and -T469I variants were more responsive to capsaicin and coal fly ash. - Molecular Bases of DiseaseOpen Access
Der f 34, a Novel Major House Dust Mite Allergen Belonging to a Highly Conserved Rid/YjgF/YER057c/UK114 Family of Imine Deaminases
Journal of Biological ChemistryVol. 291Issue 41p21607–21615Published online: August 18, 2016- Kareem Gamal ElRamlawy
- Takashi Fujimura
- Koji Baba
- Ji Won Kim
- Chika Kawamoto
- Toshihide Isobe
- and others
Cited in Scopus: 16The high prevalence of house dust mite (HDM) allergy is a growing health problem worldwide, and the characterization of clinically important HDM allergens is a prerequisite for the development of diagnostic and therapeutic strategies. Here, we report a novel HDM allergen that belongs structurally to the highly conserved Rid/YjgF/YER057c/UK114 family (Rid family) with imine deaminase activity. Isolated HDM cDNA, named der f 34, encodes 128 amino acids homologous to Rid-like proteins. This new protein belongs to the Rid family and has seven conserved residues involved in enamine/imine deaminase activity. - ImmunologyOpen Access
Leptin Enhances TH2 and ILC2 Responses in Allergic Airway Disease
Journal of Biological ChemistryVol. 291Issue 42p22043–22052Published online: August 26, 2016- Handong Zheng
- Xing Zhang
- Eliseo F. Castillo
- Yan Luo
- Meilian Liu
- Xuexian O. Yang
Cited in Scopus: 55Allergic asthma and obesity are the leading health problems in the world. Many studies have shown that obesity is a risk factor of development of asthma. However, the underlying mechanism has not been well established. In this study, we demonstrate that leptin, an adipokine elevated in obese individuals, promoted proliferation and survival of pro-allergic type 2 helper T cells and group 2 innate lymphoid cells and production of type 2 cytokines, which together contribute to allergic responses. Leptin activates mTORC1, MAPK, and STAT3 pathways in TH2 cells. - Molecular Bases of DiseaseOpen Access
Eosinophil Peroxidase Catalyzed Protein Carbamylation Participates in Asthma
Journal of Biological ChemistryVol. 291Issue 42p22118–22135Published online: September 1, 2016- Zeneng Wang
- Joseph A. DiDonato
- Jennifer Buffa
- Suzy A. Comhair
- Mark A. Aronica
- Raed A. Dweik
- and others
Cited in Scopus: 22The biochemical mechanisms through which eosinophils contribute to asthma pathogenesis are unclear. Here we show eosinophil peroxidase (EPO), an abundant granule protein released by activated eosinophils, contributes to characteristic asthma-related phenotypes through oxidative posttranslational modification (PTM) of proteins in asthmatic airways through a process called carbamylation. Using a combination of studies we now show EPO uses plasma levels of the pseudohalide thiocyanate (SCN−) as substrate to catalyze protein carbamylation, as monitored by PTM of protein lysine residues into Nϵ-carbamyllysine (homocitrulline), and contributes to the pathophysiological sequelae of eosinophil activation. - Molecular Bases of DiseaseOpen Access
Epitope Mapping of Rhi o 1 and Generation of a Hypoallergenic Variant: A CANDIDATE MOLECULE FOR FUNGAL ALLERGY VACCINES
Journal of Biological ChemistryVol. 291Issue 34p18016–18029Published online: June 28, 2016- Gaurab Sircar
- Kuladip Jana
- Angira Dasgupta
- Sudipto Saha
- Swati Gupta Bhattacharya
Cited in Scopus: 23Efficacy of allergen-specific immunotherapy is often severely impaired by detrimental IgE-mediated side effects of native allergen during vaccination. Here, we present the molecular determinants for IgE recognition of Rhi o 1 and eventually converting the allergen into a hypoallergenic immunogen to restrain health hazards during desensitization. Rhi o 1 is a respiratory fungal allergen. Despite having cross-reactivity with cockroach allergen, we observed that non-cross-reactive epitope predominantly determined IgE binding to Rhi o 1. - Molecular Bases of DiseaseOpen Access
Antigenic Determinants of the Bilobal Cockroach Allergen Bla g 2
Journal of Biological ChemistryVol. 291Issue 5p2288–2301Published online: December 7, 2015- Judith A. Woodfolk
- Jill Glesner
- Paul W. Wright
- Christopher L. Kepley
- Mi Li
- Martin Himly
- and others
Cited in Scopus: 16Bla g 2 is a major indoor cockroach allergen associated with the development of asthma. Antigenic determinants on Bla g 2 were analyzed by mutagenesis based on the structure of the allergen alone and in complex with monoclonal antibodies that interfere with IgE antibody binding. The structural analysis revealed mechanisms of allergen-antibody recognition through cation-π interactions. Single and multiple Bla g 2 mutants were expressed in Pichia pastoris and purified. The triple mutant K132A/K251A/F162Y showed an ∼100-fold reduced capacity to bind IgE, while preserving the native molecular fold, as proven by x-ray crystallography. - ImmunologyOpen Access
Basophil-associated OX40 Ligand Participates in the Initiation of Th2 Responses during Airway Inflammation
Journal of Biological ChemistryVol. 290Issue 20p12523–12536Published online: April 3, 2015- Caixia Di
- Xiaoliang Lin
- Yanjie Zhang
- Wenwei Zhong
- Yufan Yuan
- Tong Zhou
- and others
Cited in Scopus: 19Background:Basophils play a great role in the induction of Th2 cell responses in different disease contexts.Results:Basophils highly expressed OX40 ligand (OX40L) after activation. Adoptive transfer of activated basophils triggered a robust Th2 response and airway inflammation.Conclusion:Basophils primed Th2 responses via OX40-OX40L interaction in asthma.Significance:OX40L on basophils may be a novel therapeutic target in asthma.