HHSN261200800001E and by the Department of Immunology, University of Washington. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services,

nor does mention of trade names, commercial products, or organizations imply endorsement by the US government. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Dr. Dennis Klinman and members of his lab are co-inventors on a number of patents concerning CpG ODN and their use. All rights to these patents have been assigned to the Federal government. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, Venetoclax purchase but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Supporting Figure 1. Level of IRF and NF-κB transcription factors in the cytoplasm of ‘K’ ODN stimulated CAL-1 cells. CAL-1 cells were incubated with 1 μM of ‘K’ ODN for the indicated times. Cytoplasmic lysates were extracted and analyzed by immunoblotting

for changes in the concentration of (A) various IRFs and (B) NF-κB p50 and p65. Lamin and a-tubulin were used to assess cytoplasmic purity and loading. Data are representative Selleck AUY-922 of 3 independent experiments. Supporting Figure 2: Effects of siRNA knockdown on mRNA expression. CAL 1 cells were transfected with siRNA to knockdown Sucrase gene expression. A, B, C) The knockdown efficacy of the indicated siRNA was evaluated by analyzing mRNA levels by RT PCR. Changes in mRNA levels (percentage indicated) were evaluated by comparison to cells transfected with control siRNA in each experiment. D, E) CAL-1 cells were transfected with siRNA but not treated with CpG ODN. Note that IL-6 mRNA levels were unchanged in these cells. Results were determined by

RT PCR with GAPDH used as the endogenous control. Data represent the mean ± SEM of 2-3 independent experiments experiments. Supporting Figure 3. Schematic representation of proposed role of IRF-5 and NF-κB in the induction of IFNß and IL-6 by ‘K’ ODN in human pDCs. “
“A decrease in the number of dendritic cells (DCs) is a major cause of post-sepsis immunosuppression and opportunistic infection and is closely associated with poor prognosis. Increasing the number of DCs to replenish their numbers post sepsis can improve the condition. This therapeutic approach could improve recovery after sepsis. Eighty C57BL/6 mice were subjected to sham or caecal ligation and puncture (CLP) surgery. Mice were divided into 4 groups: (1) Sham + vehicle, (2) Sham + DC, (3) CLP + vehicle, and (4) CLP + DC. Bone marrow-derived DCs (BMDCs) were administered at 6 h, 12 h, and 24 h after surgery.