Anti-hBD-2 polyclonal antibody was selleck chemical purchased from Peptide International, Inc (Louisville, Kentucky, USA). Lyophilised NVP-AUY922 powder of anti-hBD-2 antibody was reconstituted to the stock concentration of 10 mg/ml with sterile phosphate buffered saline

(GIBCO BRL). Bronchial epithelium medium (BEGM) was obtained from Lonza Group Ltd (Basel, Switzerland). Maintenance of endotoxin-free conditions Experiments were designed to minimise endotoxin contamination by using purchased endotoxin-free plasticware and heating all glassware at 180°C for 4 hours. All solutions used in the experiments contained less then 0.007 endotoxin unit/ml (minimal detectable level) when tested with Limulus amebocyte lysate assay (Sigma). A. fumigatus organisms were washed in

the solution containing Polymixin B during preparation. Patient material Human nasal turbinates of patients undergoing turbinectomy selleck chemicals llc (Pr. G. Lamas, La Pitié-Salpêtrière University Hospital Centre, Paris, France) were used for the preparation of the primary epithelial cells. All patients signed an informed consent form before participating in this research protocol, which was approved by the Institutional Ethics Committee. Fungal strain and growth conditions The A. fumigatus strain, CBS 144.89 (Institut Pasteur, Paris, France), was used throughout this study. A. fumigatus conidia were prepared as previously described [22]. Briefly, conidia of A. fumigatus were obtained from cultures grown on YM agar (0.3% yeast extract, 2% malt extract, 0.5% peptone and 0.5% agar) for three days at 37°C. Conidia were harvested by flooding the plates with sterile distilled water and then suspending the hydrophobic conidia in 0.01% Tween 20 in phosphate-buffered solution (PBS). To remove hyphae and debris, the conidial

suspension was filtered through four levels of gauze. The RC obtained were maintained at 4°C. Preparation of swollen conidia and hyphal fragments SC were prepared as described [47]. Briefly, 5 × 109 of resting A. fumigatus conidia were incubated in 200 ml of Sabouraud medium for 5 hours at 37°C in order to obtain the isodiametric swelling of the conidium resulting in Suplatast tosilate the development of SC. As demonstrated by microscopic examination, the majority of the organisms were single conidia, with a few small clumps containing two to four organisms. To obtain a homogeneous preparation, the suspension was gently sonicated for 10 seconds using a Branson Sonifier 450 (output level 2; Branson Ultrasonics, Danbury, CT, USA). Before exposure of the cells to conidia, the solution was vigorously vortexed and observed microscopically to ensure the absence of clumps. Hyphal fragments (HF) were prepared by incubating 2 × 108 of resting conidium in 200 ml of Sabouraud medium for 18 hours at 37°C with shaking in order to obtain a homogenous solution of the small HF. The tubes were then centrifuged in order to spin down the pellet.