Ishida Momoko, Nishi Kosuke, Shinohara Kozue, Kunihiro Nanami, Osajima Katsuhiro, Suemitsu Tomokazu, Sugahara Takuya
Faculty of Agriculture, Ehime University, 3-5-7 Tarumi, Matsuyama, Ehime, 790-8566, Japan.
Food and Health Sciences Research Centre, Ehime University, 3-5-7 Tarumi, Matsuyama, Ehime, 790-8566, Japan.
Cytotechnology. 2017 Apr;69(2):229-244. doi: 10.1007/s10616-016-0053-4. Epub 2017 Jan 13.
Dried bonito is a preserved food used in Japan, which contains abundant flavor ingredients and functional substances. We focused on the immunostimulatory effect of dried bonito extract (DBE) on mouse macrophage-like J774.1 cells, RAW264.7 cells, and mouse primary peritoneal macrophages. DBE significantly stimulated the production of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) by both J774.1 cells and peritoneal macrophages by enhancing the cytokine gene expression levels. In addition, DBE stimulated nitric oxide production by enhancing the expression of inducible nitric oxide synthase in RAW264.7 cells. DBE also increased the phagocytosis activity of J774.1 cells. Immunoblot analysis revealed that DBE has an immunostimulatory effect on macrophages through activation of mitogen-activated protein kinase and nuclear factor-κB cascades. TNF-α production enhanced by DBE was partially inhibited by treatment with TLR4 inhibitor TAK-242, whereas IL-6 production enhanced by DBE was almost inhibited. These results suggested that DBE is thought to strongly stimulate the TLR4 signaling pathway for macrophage activation, and its activation is also involved in other signaling. Finally, the phagocytosis activity of peritoneal macrophages from DBE-administered BALB/c mice increased significantly, suggesting that DBE has the potential to stimulate macrophage activity in vivo. In conclusion, these data indicated that DBE contributes to activating host defense against pathogens by activating innate immunity.
鲣节干是一种在日本使用的腌制食品,它含有丰富的风味成分和功能物质。我们重点研究了鲣节干提取物(DBE)对小鼠巨噬细胞样J774.1细胞、RAW264.7细胞和小鼠原代腹腔巨噬细胞的免疫刺激作用。DBE通过提高细胞因子基因表达水平,显著刺激J774.1细胞和腹腔巨噬细胞产生肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)。此外,DBE通过增强RAW264.7细胞中诱导型一氧化氮合酶的表达来刺激一氧化氮的产生。DBE还增加了J774.1细胞的吞噬活性。免疫印迹分析表明,DBE通过激活丝裂原活化蛋白激酶和核因子-κB级联反应对巨噬细胞具有免疫刺激作用。用TLR4抑制剂TAK-242处理可部分抑制DBE增强的TNF-α产生,而DBE增强的IL-6产生几乎被抑制。这些结果表明,DBE被认为强烈刺激TLR4信号通路以激活巨噬细胞,并且其激活还涉及其他信号传导。最后,给予DBE的BALB/c小鼠腹腔巨噬细胞的吞噬活性显著增加,表明DBE具有在体内刺激巨噬细胞活性的潜力。总之,这些数据表明DBE通过激活先天免疫来促进激活宿主对病原体的防御。