Department of Respiratory Medicine, Gunma University Graduate School of Medicine, Gunma, Japan.
Department of Medicine and Molecular Science, Gunma University Graduate School of Medicine, Gunma, Japan.
FASEB J. 2019 Nov;33(11):12750-12759. doi: 10.1096/fj.201900283R. Epub 2019 Aug 30.
We investigated the effects of resolvin E (RvE) 1, RvE2, and RvE3 on IL-4- and IL-33-stimulated bone marrow-derived dendritic cells (BMDCs) from house dust mite (HDM)-sensitized mice. We also investigated the role of RvE3 in a murine model of HDM-induced airway inflammation. , BMDCs from HDM-sensitized mice were stimulated with IL-4 and IL-33 and then treated with RvE1, RvE2, RvE3, or vehicle. RvE1, RvE2, and RvE3 suppressed IL-23 release from BMDCs. RvE3 administrated to HDM-sensitized and challenged mice in the resolution phase promoted a decline in total numbers of inflammatory cells and eosinophils, reduced levels of IL-23 and IL-17 in lavage fluid, and suppressed and mRNA expression in lung and peribronchial lymph nodes. RvE3 also reduced resistance in the lungs of HDM-sensitized mice. A NanoBiT β-arrestin recruitment assay using human embryonic kidney 293 cells revealed that pretreatment with RvE3 suppressed the leukotriene B4 (LTB4)-induced β-arrestin 2 binding to LTB4 receptor 1 (BLT1R), indicating that RvE3 antagonistically interacts with BLT1R. Collectively, these findings indicate that RvE3 facilitates the resolution of allergic airway inflammation, partly by regulating BLT1R activity and selective cytokine release by dendritic cells. Our results accordingly identify RvE3 as a potential therapeutic target for the management of asthma.-Sato, M., Aoki-Saito, H., Fukuda, H., Ikeda, H., Koga, Y., Yatomi, M., Tsurumaki, H., Maeno, T., Saito, T., Nakakura, T., Mori, T., Yanagawa, M., Abe, M., Sako, Y., Dobashi, K., Ishizuka, T., Yamada, M., Shuto, S., Hisada, T. Resolvin E3 attenuates allergic airway inflammation the interleukin-23-interleukin-17A pathway.
我们研究了 resolvin E (RvE) 1、RvE2 和 RvE3 对屋尘螨(HDM)致敏小鼠骨髓来源树突状细胞(BMDC)中 IL-4 和 IL-33 刺激的影响。我们还研究了 RvE3 在 HDM 诱导的气道炎症小鼠模型中的作用。从 HDM 致敏的小鼠中分离出 BMDC,用 IL-4 和 IL-33 刺激,然后用 RvE1、RvE2、RvE3 或载体处理。RvE1、RvE2 和 RvE3 抑制 BMDC 释放 IL-23。在解决阶段向 HDM 致敏和 challenged 小鼠施用 RvE3 可促进炎症细胞和嗜酸性粒细胞总数减少,减少灌洗液中 IL-23 和 IL-17 的水平,并抑制肺和支气管周围淋巴结中的 和 mRNA 表达。RvE3 还降低了 HDM 致敏小鼠肺部的阻力。使用人胚肾 293 细胞进行的 NanoBiT β- arrestin 招募测定表明,RvE3 预处理可抑制白细胞三烯 B4(LTB4)诱导的 β-arrestin 2 与 LTB4 受体 1(BLT1R)结合,表明 RvE3 拮抗地与 BLT1R 相互作用。总之,这些发现表明 RvE3 通过调节树突状细胞的 BLT1R 活性和选择性细胞因子释放,促进过敏性气道炎症的消退。我们的研究结果相应地确定 RvE3 是管理哮喘的潜在治疗靶标。-Sato, M., Aoki-Saito, H., Fukuda, H., Ikeda, H., Koga, Y., Yatomi, M., Tsurumaki, H., Maeno, T., Saito, T., Nakakura, T., Mori, T., Yanagawa, M., Abe, M., Sako, Y., Dobashi, K., Ishizuka, T., Yamada, M., Shuto, S., Hisada, T. Resolvin E3 attenuates allergic airway inflammation the interleukin-23-interleukin-17A pathway.