Department of Molecular and Medical Biotechnology, Kangwon National University, Chuncheon, Republic of Korea.
J Microbiol. 2010 Aug;48(4):512-7. doi: 10.1007/s12275-010-0053-6. Epub 2010 Aug 20.
Bacterial CpG motifs are known to induce both innate and adaptive immunity in infected hosts via toll-like receptor 9 (TLR9). Because small oligonucleotides (ODNs) mimicking bacterial CpG motifs are easily synthesized, they have found use as immunomodulatory agents in a number of disease models. We have developed a novel bioinformatics approach to identify effective CpG ODN sequences and evaluate their function as TLR9 ligands in a murine system. Among the CpG ODNs we identified, M5-30 and M6-395 showed significant ability to stimulate TNF-alpha and IFN-gamma production in a mouse macrophage cell line and mouse splenocytes, respectively. We also found that these CpG ODNs activated cells through the canonical NF-kappa B signaling pathway. Moreover, both CpG ODNs were able to induce Th1-mediated immunity in Mycobacterium tuberculosis (Mtb)-infected mice. Our results demonstrate that M5-30 and M6-395 function as TLR9-specific ligands, making them useful in the study of TLR9 functionality and signaling in mice.
细菌 CpG 基序通过 Toll 样受体 9(TLR9)已知可诱导感染宿主的先天和适应性免疫。由于模拟细菌 CpG 基序的小寡核苷酸(ODN)易于合成,因此它们已在许多疾病模型中用作免疫调节剂。我们开发了一种新的生物信息学方法来鉴定有效的 CpG ODN 序列,并在小鼠系统中评估它们作为 TLR9 配体的功能。在我们鉴定的 CpG ODN 中,M5-30 和 M6-395 分别在小鼠巨噬细胞系和小鼠脾细胞中显示出刺激 TNF-α和 IFN-γ产生的显著能力。我们还发现这些 CpG ODN 通过经典的 NF-κB 信号通路激活细胞。此外,这两种 CpG ODN 都能够在感染结核分枝杆菌(Mtb)的小鼠中诱导 Th1 介导的免疫。我们的结果表明 M5-30 和 M6-395 作为 TLR9 特异性配体发挥作用,使它们在研究 TLR9 在小鼠中的功能和信号转导方面具有应用价值。