Synergistic Effect of Dermatophagoides farinae and Lipopolysaccharides in Human Middle ear Epithelial Cells.
10.4168/aair.2016.8.5.445
- Author:
Ji Eun LEE
1
;
Yeon Hoo KIM
;
Chae Seo RHEE
;
Dong Young KIM
Author Information
1. Department of Otorhinolaryngology-Head and Neck Surgery, Chosun University College of Medicine, Gwangju, Korea.
- Publication Type:Original Article
- Keywords:
Dermatophagoides farinae;
innate immunity;
lipopolysaccharides;
mucins;
toll-like receptors
- MeSH:
Allergens;
Cytokines;
Dermatophagoides farinae*;
Ear, Middle*;
Epithelial Cells*;
Granulocyte-Macrophage Colony-Stimulating Factor;
Humans*;
Hypersensitivity;
Immunity, Innate;
In Vitro Techniques;
Lipopolysaccharides*;
Mucins;
Otitis Media with Effusion;
Pyroglyphidae*;
Real-Time Polymerase Chain Reaction;
RNA, Messenger;
Toll-Like Receptors
- From:Allergy, Asthma & Immunology Research
2016;8(5):445-456
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Although the concept of "one airway, one disease," which includes the middle ear space as part of the united airway is well recognized, the role of allergens in otitis media with effusion (OME) is not clearly understood. We aimed to investigate the effect of the interaction between Dermatophagoides farinae (Der f) and lipopolysaccharide (LPS) on the induction of epithelial inflammatory response in vitro. METHODS: Primary human middle ear epithelial cells were exposed to Der f, LPS, or both in different sequences, and the magnitude of the immunologic responses was compared. The mRNA expressiona of mucin (MUC) 4, 5AC, 5B, 8, GM-CSF, TNF-α, TLR4, and MD-2 were evaluated using real-time PCR. MUC levels before and after siRNA-mediated knockout of TLR4 and MD-2 were assessed. Lastly, the involved cell signaling pathway was evaluated. RESULTS: The expressiona of cytokines, and the MUC 4, 5AC, 5B, and 8 genes were augmented by pretreatment with Der f followed by LPS; however, reverse treatment or combined treatment did not induce the same magnitude of response. Increased MUC expression was decreased by TLR4 knockdown, but not by MD-2 knockdown. The signal intensity of MUC 8 was higher in MD-2 over-expressed cells than in those exposed to LPS only. The translocation of nuclear factor-κB was observed in cells pretreated with Der f followed by LPS. CONCLUSIONS: When Der f treatment preceded LPS exposure, Der f and LPS acted synergistically in the induction of pro-inflammatory cytokines and the MUC gene, suggesting an important role in the development of OME in patients with concealed allergy airway sensitization.
