Scientific Reports · 2012 · 59 citations · 52 references
Life SciencesImmunologyMolecular BiologyCell SignalingInnate ImmunitySignal TransductionInflammatory SignalingInnate Immune ActivationInnate Immune Signaling PathwaysInterferon ResponsesLigand BindingToll-like ReceptorsBifurcationImmune Response To NanomaterialsImmune System InteractionsInflammatory Responses To NanoparticlesPhosphodiester BackbonePhosphodiester OligonucleotidesToll-like Receptor SignalingToll-like Receptor-mediated Cytokine Induction
The interaction of cytosine-phosphate-guanine oligodeoxynucleotides (CpG ODNs) with Toll-like receptor 9 (TLR9) activates the immune system. Multimeric class A CpG ODNs induce interferon-α (IFN-α) and, to a lesser extent, interleukin-6. By contrast, monomeric class B CpG ODNs induce interleukin-6 but not IFN-α. This difference suggests that the multimerization of CpG ODN molecules is a key factor in IFN-α induction. We multimerized class B CpG ODN2006x3-PD molecules that consist entirely of a phosphodiester backbone onto quantum dot silicon nanoparticles with various binding modes. Herein, we present the binding mode-dependent bifurcation of cytokine induction and discuss its possible mechanism of CpG ODN and TLR9 interaction. Our discoveries also suggest that nanoparticles play roles in not only delivery of CpG ODNs but also control of CpG ODN activity.
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