Bright fluorescence www.selleckchem.com/screening/epigenetics-compound-library.html signals were seen for all preparations used in this study. No signal was found for beads carrying only MAb 3/1 or MAb 26/1, respectively. Additionally, coated beads were tested for the presence of the housekeeping proteins Mip,

Hsp60 and OmpM using specific MAbs and isotype-specific anti-mouse FITC. These proteins are constituent parts of OMV (Helbig et al., 2006a). Soluble LPS-carrying beads were negative; on OMV beads, a weak OmpM signal was detectable. Mip and Hsp60 were negative (immunofluorescence data not shown). Using the chosen technique, it was possible to decorate the beads separately according to the strains, the growth phases and the LPS fractions. The strain-unspecific

LPS decoration of beads visualized by Oh & Swanson (1996) revealed that synthetic Selleck AZD8055 particles were not delivered to lysosomes efficiently, presumably because of their hydrophobicity. Therefore, we used beads without LPS, but coated with specific antibodies as a reference parameter for statistical evaluation in order to assess only the additional inhibition power due to LPS. The percentage of uncoated lysosomal beads found after 1 h (after 5 h) amounted to 45.5±5.1% (41.8±1.9%) in A. castellanii, 32.4±2.2% (28.5±5.9%) in human monocytes and 30.0±5.1% (27.1±4.9%) in A/J mouse macrophages. For standardization, the counted number of uncoated beads in host cells (average±SD) per experiment was calculated to be 100% (±SD). With reference to the uncoated beads, 1 h after phagocytosis, 77.7±10.4% of beads carrying Corby OMV prepared from the E-phase were colocalized with lysosomal FDx inside A. castellanii (Fig. 1a). The value for Corby TF 3/1 amounted to 75.9±12.0%. Both strains do not differ significantly from negative controls and themselves. Beads coated with LPS fraction

<300 kDa were located in smaller numbers (P<0.001) in lysosomes of A. castellanii, 26.9±3.3% of the Corby strain and 32.5±4.7% of the mutant TF 3/1. We obtained similar results for human monocytes. A/J mouse macrophages also fulfil the chosen significance level (P<0.001), but in comparison with A. castellanii and monocytes, more than twice as many of beads for are lysosomal. An attempt at explaining these differences is not possible with the study design chosen. OMV and LPS fractions <300 kDa prepared from PE-phase liquid cultures of both strains inhibited phagosome maturation sufficiently 1 h after phagocytosis. We achieved statistically significant differences (P up to <0.001) for all host cells (Fig. 1b). Certainly, the significance level was lower for OMV than for LPS fraction <300 kDa regardless of the strains and host cells, but these calculations could have been due to the study design. OMV have a diameter of 186±83 nm (Fernandez-Moreira et al., 2006).