The method13 was used to calculate relative changes in gene expression determined from quantitative reverse transcription-PCR (qRT-PCR) experiments. Microarray analysis on RNA extracted from C2-M cells incubated with L. salivarius, E.coli, B. fragilis or beads for 2 hr was performed by Cogenics (Beckman Coulter Genomics, Takeley, UK). Briefly, biotinylated cRNA was generated according to manufacturer’s instructions (Affymetrix, Santa Chk inhibitor Clara, CA), hybridized to Human

Genome U133 Plus 2.0 Arrays (Affymetrix), washed and fluorescently labelled. The Affymetric GeneChips® were then scanned using the Affymetrix GeneChip Scanner 3000 and quantified using GeneChip Operating software (Affymetrix). For each ProbeSet, a ‘detection call’ was provided indicating whether the transcript was considered to be ‘present’, ‘absent’, or marginal. The GeneChip files were further analysed using GeneSpring 7.3.1 software (Silicon Genetics, Agilent Technologies, Santa Clara, CA). Hierarchical cluster analysis and visualization were performed using Genesis.14 All microarray data described in this study have been deposited in the National Center for Biotechnology Information Gene Expression Omnibus database with the accession number GSE25330. Measurement of secreted human interleukin-1β (IL-1β), IL-6,

IL-8 and tumour necrosis factor-α (TNF-α) in culture supernatants was performed using an electro-chemiluminescence multiplex system Sector 2400 imager from Meso Scale Discovery (Gaithersburg, MD) where antibodies labelled with

SULFO-TAG™ reagents Cyclin-dependent kinase 3 emitted light Seliciclib mouse upon electrochemical stimulation. Lactobacillus salivarius, E. coli and B. fragilis were resuspended in PBS at a concentration of 1 × 109/ml, labelled with 1 mmBacLight™ Red bacterial stain (Molecular Probes) and finally resuspended in 100 μl PBS to give a concentration of 1 × 109 bacteria/100 μl. BALB/c mice were orally gavaged with 100 μl BacLight-labelled bacteria or control beads and were killed 2 hr after gavage. Intestines were dissected out and one 2-cm intestinal section containing a Peyer’s patch was frozen in liquid nitrogen for each experimental condition. Remaining Peyer’s patches were removed and placed in DMEM supplemented with 10% FBS, 100 μg/ml penicillin and 100 U/ml streptomycin and 2·5 μg/ml Fungizone® (Gibco) for isolation of M cells. The follicle-associated epithelium was isolated from murine Peyer’s patches according to previously published methods.15 M cells were isolated by positive magnetic bead selection using the magnetic antibody cell-sorting (MACS) system (Miltenyi Biotech, Surrey, UK). Follicle-associated epithelial cells were resuspended in 0·01% EDTA for 15 min, filtered through a 30-μm cup Filcon cell filter (BD Biosciences) to remove cell aggregates and the filtrate was centrifuged and resuspended in degassed sample buffer [1 × PBS containing 0·5% BSA (Sigma) and 2 mm EDTA] at a concentration of 1 × 107 cells/100 μl.