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Binding Mode of CpG Oligodeoxynucleotides to Nanoparticles Regulates Bifurcated Cytokine induction via Toll-like Receptor 9

机译:CpG寡脱氧核苷酸与纳米粒子的结合模式调节通过Toll样受体9分叉的细胞因子诱导。

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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.. ? 2012 Macmillan Publishers Limited. All rights reserved
机译:胞嘧啶-磷酸-鸟嘌呤寡聚脱氧核苷酸(CpG ODN)与Toll样受体9(TLR9)的相互作用激活了免疫系统。多聚体A类CpG ODN诱导干扰素-α(IFN-α),并在较小程度上诱导白介素6。相比之下,单体B类CpG ODN诱导白介素6而不诱导IFN-α。这种差异表明,CpG ODN分子的多聚化是诱导IFN-α的关键因素。我们将完全由磷酸二酯主链组成的B类CpG ODN2006x3-PD分子多聚于具有各种结合模式的量子点硅纳米颗粒上。在这里,我们介绍细胞因子诱导的结合模式依赖性分叉,并讨论其CpG ODN和TLR9相互作用的可能机制。我们的发现还表明,纳米颗粒不仅在CpG ODN的传递中起着作用,而且在CpG ODN活性的控制中也起着作用。 2012 Macmillan Publishers Limited。版权所有

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