The induction was higher in H5N1 infection than that of seasonal H1N1 infection. Moreover, TGF-β2, which plays an important role in regulating inflammatory processes, was identified as a target of miR-141 binding. As a result, influenza A virus infection, in particular highly pathogenic H5N1, could affect the inflammatory GF120918 processes via miR-141 induction. Methods Virus isolates The influenza A H5N1 virus (A/Thai/KAN1/2004) (H5N1/2004) was isolated from a patient with fatal

infection in Thailand in 2004. To serve as a comparison, a human seasonal H1N1 strain isolated in 2002 – (A/HongKong/CUHK-13003/2002) (H1N1/2002) was included. The research use of these samples was approved by the Joint CUHK – NTEC Research Ethics Committee, Hong Kong and the strains were Tariquidar price isolated from the patients as part of standard care. Cell cultures The bronchial epithelial cells – NCI-H292, derived from human lung mucoepidermoid carcinoma cells (ATCC, CRL-1848, Rockville, MD, USA), were grown

as monolayers in RPMI-1640 medium (Invitrogen, Carlsbad, CA) supplemented with 10% fetal bovine serum (FBS), 100 U/ml penicillin and 100 μg/mL streptomycin (all from Gibco, Life Technology, Rockville, Md., USA) at 37°C in a 5% CO2 incubator. NCI-H292 cells were used as an in- vitro model to study host cellular responses to viral infection. Mandin-Darby canine kidney (MDCK) cells were used for growing stocks of influenza virus isolates. MDCK cells were grown and maintained in Eagles Minimal Essential Media (MEM) containing 2% FBS, 100 U/ml penicillin and 100 μg/mL streptomycin (all from Gibco, Life Technology). Infection of cell culture with influenza A viruses NCI-H292 cells were grown to confluence in sterile T75 tissue culture flasks for the inoculation of virus isolate at a multiplicity of

infection (m.o.i.) of one. After 1 hour of absorption, the virus was removed and 2 ml of fresh RPMI-1640 media with 2% FBS, 100 U/ml penicillin, 100 μg/mL streptomycin and 1μg/ml L-1-tosylamido-2-phenylethyl chloromethyl ketone (TPCK)-treated trypsin (all from Gibco, Life Technology) was added, and incubated at 37°C in 5% CO2 humidified air. RNA extraction Total RNA was extracted from normal and infected Arachidonate 15-lipoxygenase NCI-H292 cells using Trizol reagent (Invitrogen) following the manufacturer’s protocol. RNA pellets were resuspended in RNase-free water. The RNA integrity was assessed using CA4P Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA). MiRNA expression profiling MiRNAs were labeled using the Agilent miRNA labeling reagent and hybridized to Agilent human miRNA arrays according to the manufacturer’s protocol. Briefly, total RNA (100 ng) was dephosphorylated and ligated with 3′, 5′-cytidine bisphosphate (pCp-Cy3). Labeled RNA was purified and hybridized to Agilent miRNA arrays with eight identical arrays per slide, with each array containing probes interrogating 866 human miRNAs.