Department of Synthetic Biology and Immunology, National Institute of Chemistry, Hajdrihova 19, SI-1001 Ljubljana, Slovenia.
EN-FIST Centre of Excellence, Trg Osvobodilne fronte 13, SI-1000 Ljubljana, Slovenia.
Nat Commun. 2017 May 22;8:15363. doi: 10.1038/ncomms15363.
Toll-like receptors encounter a diversity of degradation products in endosomes. TLR7 and TLR8 have been shown to be activated by RNA degradation products. Here we show that although TLR9 requires single-stranded DNA longer than 20 nucleotides for a robust response, TLR9 activation is augmented by CpG-containing oligodeoxyribonucleotides (sODNs) as short as 2 nucleotides, which, by themselves, do not induce activation in cell cultures, as well as in mice. sODNs also activate human TLR9 in combination with ODNs containing a single CpG motif that by themselves do not activate human TLR9. The specific sequence motif of sODN and colocalization of ODN and sODN suggest that the mechanism of activation involves binding of both ODN and sODN to TLR9. sODNs augment TLR9 activation by mammalian genomic DNA indicating the role of short DNA degradation products in the endosomes in response to infection or in autoimmune disease, particularly at limiting concentrations of ODNs.
Toll 样受体在内涵体中遇到多种降解产物。已经证明 TLR7 和 TLR8 可被 RNA 降解产物激活。在这里,我们表明尽管 TLR9 需要 20 个核苷酸以上的单链 DNA 才能产生强烈的反应,但含有 CpG 的寡脱氧核糖核苷酸(sODN),即使短至 2 个核苷酸,也能增强 TLR9 的激活,这些 sODN 本身不会在细胞培养物以及小鼠中诱导激活。sODN 还可与含有单个 CpG 基序的 ODN 联合激活人 TLR9,而这些 ODN 本身不会激活人 TLR9。sODN 的特定序列基序和 ODN 与 sODN 的共定位表明,激活机制涉及 ODN 和 sODN 与 TLR9 的结合。sODN 增强了哺乳动物基因组 DNA 对 TLR9 的激活作用,表明在应对感染或自身免疫性疾病时,内涵体中的短 DNA 降解产物在有限浓度的 ODN 中发挥作用。