Matsuda Miyu, Mochizuki Shinichi
Department of Chemistry and Biochemistry, The University of Kitakyushu, 1-1 Hibikino, Wakamatsu-ku, Kitakyushu, Fukuoka, 808-0135, Japan.
Biochem Biophys Rep. 2023 Nov 3;36:101573. doi: 10.1016/j.bbrep.2023.101573. eCollection 2023 Dec.
Among several types of CpG-ODNs, A/D-type CpG-ODNs have potent adjuvant activity to induce Th-1 immune responses, but exhibit a propensity to aggregate. For the clinical application of A/D-type CpG-ODNs, it is necessary to control such aggregation and obtain a comprehensive understanding of the relationship between their structure and the immune responses. This study revealed that a representative A/D-type CpG ODN, D35, adopted a single-stranded structure in water, while it assembled into aggregates in response to Na ions. From polyacrylamide gel electrophoresis and circular dichroism analyses, D35 adopted a homodimeric form (duplex) via palindromic sequences in low-Na-concentration conditions (10-50 mM NaCl). After replacement of the solution with PBS, quadruplexes began to form in a manner coordinated by Na, resulting in large aggregates. The duplexes and small aggregates prepared in 50 mM NaCl showed not only high cellular uptake but also high affinity to Toll-like receptor 9 (TLR9) proteins, leading to the production of a large amount of interferon-α for peripheral blood mononuclear cells. The much larger aggregates prepared in 100 mM NaCl were incorporated into cells at a high level, but showed a low ability to induce cytokine production. This suggests that the large aggregates have difficulty inducing TLR9 dimerization, resulting in loss of the stimulation of the cells. We thus succeeded in inducing adequate innate immunity by controlling and adjusting the formation of D35 aggregates. Therefore, the findings in this study for D35 ODNs could be a vital research foundation for applications.
在几种类型的CpG-ODN中,A/D型CpG-ODN具有强大的佐剂活性,可诱导Th-1免疫反应,但有聚集倾向。对于A/D型CpG-ODN的临床应用,有必要控制这种聚集,并全面了解其结构与免疫反应之间的关系。本研究表明,代表性的A/D型CpG ODN D35在水中呈单链结构,而在钠离子作用下会组装成聚集体。通过聚丙烯酰胺凝胶电泳和圆二色性分析,D35在低钠浓度条件(10 - 50 mM NaCl)下通过回文序列形成同源二聚体形式(双链体)。用PBS替换溶液后,四链体开始以由钠协调的方式形成,导致形成大的聚集体。在50 mM NaCl中制备的双链体和小聚集体不仅显示出高细胞摄取率,而且对Toll样受体9(TLR9)蛋白具有高亲和力,从而导致外周血单核细胞产生大量干扰素-α。在100 mM NaCl中制备的大得多的聚集体能高水平地被细胞摄取,但诱导细胞因子产生的能力较低。这表明大聚集体难以诱导TLR9二聚化,导致细胞刺激丧失。因此,我们通过控制和调节D35聚集体的形成成功诱导了适当的先天免疫。所以,本研究中关于D35 ODN的发现可能是应用的重要研究基础。