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pubmed-article:15661046pubmed:abstractTextDendritic cells (DC) are professional APC that have an extraordinary capacity to prime naive T cells. It has been reported that human DC subsets express distinct toll-like receptor (TLR), which influences their function. In mice, we observed that plasmocytoid DC (pDC) express a higher level of TLR9 compared with myeloid DC (mDC) cultured with GM-CSF. However, we demonstrated that stimulation with IFN-gamma is capable of upregulating TLR9 expression in mDC to a level comparable with expression in pDC. Consistent with this observation, IL-12 p40 and IL-6 mRNA expression and IL-12 p70 secretion in response to CpG-oligodeoxynucleotides are enhanced in mDC pretreated with IFN-gamma compared with untreated cells. Therefore, TLR-mediated responses of DC subsets may be influenced not only by signals delivered by pathogens but also by regulatory signals from cytokines such as IFN-gamma.lld:pubmed
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pubmed-article:15661046pubmed:articleTitleIFN-gamma overcomes low responsiveness of myeloid dendritic cells to CpG DNA.lld:pubmed
pubmed-article:15661046pubmed:affiliationDepartment of Microbiology and Immunology, Hamamatsu University School of Medicine, Hamamatsu, Japan.lld:pubmed
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pubmed-article:15661046pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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