Moreover, infection of BMDCs

with a plasmid-cured apathogenic Yersinia enterocolitica strain lead to DC Protein Tyrosine Kinase inhibitor swelling in a MOI (multiplicity of infection) dependent manner (data not shown) indicating that bacterial LPS is responsible for DC swelling in response to contact with bacteria. Additionally, LPS-induced DC swelling was dependent on the LPS concentration used (data not shown). Moreover, we found that LPS-induced DC swelling (Fig. 1a) and CCL21-directed migration (Fig. 1b) were impaired in TLR4-deficient DCs when compared to WT DCs. These results indicate that the observed cell swelling is critically dependent on TLR4 signaling upon LPS binding. Our results are supported by another in vitro study demonstrating that stimulation of TLR4 by LPS, but neither stimulation of TLR2 by PamCys or heat-killed gram-positive bacteria nor activation of BMDCs by different cytokines (TNFα, IL-10) induce the loss of podosomes, and thereby enhance the migratory capacity of DCs [6]. However, it cannot completely be excluded that LPS-induced DC swelling occurs independently of DC migration. Moreover, cell swelling itself is not causative for DC migration since BMDCs treated with 20% H2O for 4 hr did not migrate along a chemokine gradient (data not shown). It has been described

that treatment with LPS for 24 hr increases the expression of CCR7, the receptor of the chemokines CCL19 and CCL21, on DCs [22]. Hence, possibly differences in the CCR7-expression on DC between WT and TLR4−/− DC might affect CCL21-directed INCB024360 datasheet migratory activities of these two cell types. As a consequence, BMDCs of WT and TLR4−/− mice were treated or not with LPS for 4 hr, double-stained with fluorescent antibodies against CD11c and CCR7, respectively, and analyzed by flow cytometry (data not shown). No differences were detected in the CCR7 expression rates between WT and TLR4-deficient DC kept in medium without LPS (12.5 ± 3.4% Verteporfin purchase vs. 12.4 ± 4.3%). However, after incubation with LPS (500 ng/mL) for 4 hr, CCR7 expression on DC was higher in WT than in TLR4−/− DCs (25.2 ± 4.8% vs. 17.4 ± 4.0%) suggesting that the LPS-induced

increase in CCR7 expression in WT DC contributes to LPS-induced migration. Intracellular Ca2+ acts as a key regulator of actin assembly thereby affecting the migratory activity of DCs [19]. For example, within minutes after exposure of DCs to gram-negative bacteria or LPS the cytosolic Ca2+ levels increase involving both mechanisms, entry of extracellular Ca2+ and the release of Ca2+ from intracellular stores [7, 20]. Elevated Ca2+ in turn causes extensive actin-based cytoskeletal rearrangement including loss of podosomes thereby facilitating the conversion of DCs to a migratory phenotype [6]. After treatment of DCs with LPS, we observed an increase in [Ca2+]i within 30–120 min (Fig. 2b). Increased [Ca2+]i in migrating cells may result from activation of mechanosensitive Ca2+ channels by the growing lamellipodium at the front part and gradual cell swelling [19].