We confirmed these results using TLR2-/- DCs and TLR4-/- DCs. OmpA-sal treated TLR2-/- DCs or TLR4-/- DCs Sapanisertib datasheet and then analyzed IL-12 production by ELISA. We found that OmpA-sal-treated TLR4-/- DCs had no IL-12 production. These results suggest that OmpA-sal induced the maturation and activation of DCs via a TLR4-mediated signaling pathway. Conclusions We demonstrated that OmpA-sal is a potent antigen and initiates a specific Th1 immune response in vitro. Further understanding of the mechanism by which OmpA-sal activates DC maturation and activation may facilitate the development of effective S. enterica serovar Typhimurim vaccines and an effective immunotherapeutic

adjuvant for other infectious diseases. Methods Animals Male 6-8 week old C57BL/6 (H-2Kb and I-Ab) and BALB/c (H-2Kd and I-Ad) mice were purchased from the Korean Institute of Chemistry Technology (Daejeon, Korea). Reagents and Antibodies Recombinant mouse (rm)GM-CSF and rmIL-4 were purchased from R&D Systems. Selleckchem PF2341066 Dextran-FITC and LPS (from Escherichia coli 055:B5) were obtained from Sigma-Aldrich. An endotoxin filter (END-X) and an endotoxin removal resin (END-X

B15) were acquired from Associates of Cape Cod. Cytokine ELISA kits for PD0332991 solubility dmso murine IL-12 p70, IL-4, IL-10, and IFN-γ were purchased from BD Pharmingen. FITC- or PE-conjugated monoclonal antibodies (mAbs; BD Pharmingen) were used for flow cytometry to detect CD11c (HL3), CD80 (16-10A1), CD86 (GL1), IAb β-chain (AF-120.1), H2Kb (AF6-88.5), IL-12 p40/p70 (C15.6), and IL-10 (JESS-16E3). Anti-phospho-ERK1/2, anti-phospho-p38 MAPK, anti-phospho-JNK1/2, anti-ERK1/2, anti-JNK1, and Dimethyl sulfoxide anti-p38

MAPK mAb were purchased from Cell signaling. Isotype-matched control mAbs and biotinylated anti-CD11c (N418) mAb were purchased from BD Pharmingen. Preparation of OmpA-sal The full-length OmpA-sal gene (X02006.1) was amplified by PCR, and a chromosomal preparation of X02006.1 was used as a PCR substrate. The upstream primer, 5′-GCGGATCCCACGA AGCCGGAGAA-3′, was designed to carry the EcoRI restriction site. The downstream primer, 5′-GCAAGCTTAGAAACGATAGCC-3′, carried the HindIII restriction site. PCR products digested with EcoRI and HindIII were ligated into the pMAL™ expression vector (New England Biolabs Inc.). E. coli BL21 (DE3)/pMAL™ harboring a ompA-Sal gene was grown in Luria-Bertani (LB) medium at 37°C. Recombinant proteins were over-expressed by a bacteria protein expression system [27]. The quantity of OmpA endotoxin was ≤0.01 ng/mg. Generation and culture of DCs DCs were generated from murine whole bone marrow (BM) cells. Briefly, the BM was flushed from the tibiae and femurs of BALB/c mice and depleted of red blood cells with ammonium chloride.