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J Mycol Med ; 28(2): 349-354, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29525270

ABSTRACT

OBJECTIVE: The aims of this study were to determine the role of live and heat-killed Aspergillus fumigatus conidia in releasing interleukin (IL)-25, IL-33 and thymic stromal lymphopoietin (TSLP) and to express Toll-like receptor (Tlr)2 and Tlr4 genes. MATERIALS AND METHODS: Murine lung epithelial cells were incubated with live and heat-killed A. fumigatus conidia at 37°C for 6, 24 and 48h. After treatments, ELISA was performed to measure the concentrations of IL-25, IL-33 and TSLP in the supernatants. Quantitative real-time PCR (qPCR) was performed to assess the expression levels of Tlr2 and Tlr4 genes. RESULTS: The concentrations of IL-25 and IL-33 significantly increased after exposure to live and heat-killed conidia for various times when compared with untreated control (P<0.05). The secretion of TSLP at different concentrations of heat-killed conidia was significantly higher than both live conidia and untreated control (P<0.05). qRT-PCR results indicated a up-regulation from 1.08 to 3.60-fold for Tlr2 gene expression and 1.20 to 1.80-fold for Tlr4 gene expression exposed to heat-killed conidia. CONCLUSION: A. fumigatus has a potential ability to stimulate murine lung epithelial cells to produce IL-25/IL-33/TSLP, as well as to express Tlr2/Tlr4 genes, indicating an important role of lung epithelial cells in innate immune responses to A. fumigatus interaction.


Subject(s)
Aspergillus fumigatus/immunology , Cytokines/biosynthesis , Epithelial Cells/immunology , Interleukin-17/biosynthesis , Interleukin-33/biosynthesis , Toll-Like Receptor 2/genetics , Toll-Like Receptor 4/genetics , Animals , Cell Line , Cytokines/immunology , Enzyme-Linked Immunosorbent Assay , Epithelial Cells/microbiology , Immunity, Innate , Interleukin-17/immunology , Interleukin-33/immunology , Lung/cytology , Mice , Real-Time Polymerase Chain Reaction , Spores, Fungal/immunology , Thymic Stromal Lymphopoietin
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