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

被引:46
作者
Chinnathambi, Shanmugavel [3 ]
Chen, Song [4 ]
Ganesan, Singaravelu [3 ]
Hanagata, Nobutaka [1 ,2 ]
机构
[1] Natl Inst Mat Sci, Nanotechnol Innovat Stn, Tsukuba, Ibaraki 3050047, Japan
[2] Hokkaido Univ, Grad Sch Life Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[3] Anna Univ, Dept Med Phys, Madras 600025, Tamil Nadu, India
[4] JSPS, Chiyoda Ku, Tokyo 1028472, Japan
基金
日本学术振兴会;
关键词
INDUCIBLE PROTEIN-10 PRODUCTION; SILICON NANOCRYSTALS; BACTERIAL-DNA; QUANTUM DOTS; IN-VITRO; ACTIVATION; MOTIFS; CELLS; PHARMACOKINETICS; OLIGONUCLEOTIDES;
D O I
10.1038/srep00534
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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-alpha (IFN-alpha) and, to a lesser extent, interleukin-6. By contrast, monomeric class B CpG ODNs induce interleukin-6 but not IFN-alpha. This difference suggests that the multimerization of CpG ODN molecules is a key factor in IFN-alpha 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.
引用
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页数:9
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