fumigatus. In some

experiments, the cells were exposed to 106 unfixed live conidia for 18 hours. To be sure that the inducible expression of defensins was specific to A. fumigatus and did not simply reflect a phagocytosis response, latex beads were used as a control, selleck compound since it was shown that the respiratory cells are capable of internalising nonspecific particles such as latex beads [52]. Compared to the concentration of conidia, up to a five-fold higher concentration of latex beads was used in the experiments, as suggested [30]. Before exposing the cells to the A. fumigatus organisms, the solutions were vigorously vortexed and observed microscopically to ensure that they did not contain clumps. RNA isolation and analysis of defensin expression by

RT-PCR In order to ensure that the cells were exposed to different morphotypes of A. fumigatus organisms (conidia or HF) during the incubation period, the cell culture was observed microscopically at the beginning and at the end of the exposure. The medium was selleck kinase inhibitor discarded, the wells were briefly washed with PBS solution, and TRIzol reagent was added to the cells. Total RNA was isolated with TRIzol Reagent (Invitrogen, Cat N 15596-026) according to the manufacturer’s instructions. RNA was precipitated with ethanol and resuspended in diethyl pyrocarbonate H20. The RNA concentration was measured by spectroscopy, and the integrity of RNA was assessed on CBL0137 an agarose gel. cDNA was synthesized from 1 μg of purified RNA, using 50 nM of Oligo dT, 16 mer, (Operon Biotechnologies SP230), 30 units of AMV Reverse Transcriptase (Promega M5108) and RNA-se free H20 in a reaction volume of 25 μl, according to the manufacturer’s recommendations. Identical reactions devoid of reverse transcriptase (-RT) were carried out in parallel and did not lead to any DNA amplification of predicted molecular weight in contrast to reverse transcriptase-containing reactions. Reactions containing H20 instead of cDNA were also used in negative controls (data not shown). A RT-PCR approach was used for the analysis of defensin expression in A549 and 16HBE human respiratory Selleck MK-3475 cell lines, as well as in primary culture of human respiratory

cells exposed to RC, SC, or HF. Gene-specific primers for hBD1 and hBD2 were designed according to the sequences available at the National Center for Biotechnology Information http://​www.​ncbi.​nlm.​nih.​gov/​ in order to amplify specific cDNA sequences and avoid genomic DNA amplification. In this respect, primer sequences were designed to cover at least two subsequent exons, the human beta-defensin (HBD) -1 and -2 (NCBI accession # NM 005218.3 and NM 004942.2, respectively). It should be observed that hBD2 is now referred to as hBD-4 in the NCBI database. However, we decided to use the term, hBD2, since it is widely used in scientific literature today [53]. For the analysis of hBD8, hBD9 and hBD18, we relied on previous studies; the primers and PCR conditions were used as described in [10].