Zhai Tianhang, Sun Yue, Li Huidan, Zhang Jie, Huo Rongfen, Li Haichuan, Shen Baihua, Li Ningli
Shanghai Institute of Immunology & Department of Immunology and Microbiology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Institute of Immunology & Department of Immunology and Microbiology, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Department of Rheumatology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, China.
J Pharmacol Sci. 2016 Mar;130(3):143-50. doi: 10.1016/j.jphs.2015.12.007. Epub 2016 Jan 8.
It has been widely accepted that macrophages are divided into M1 "pro-inflammatory" macrophages and M2 "anti-inflammatory" macrophages and an uncontrolled macrophage polarization plays an important role in the pathogenesis of different diseases. As the main substance of total glucosides of peony, paeoniflorin (PF), has been widely used to treat autoimmune and autoinflammatory diseases for years. Mechanistically, PF has been found to alter activities of many immune cells, which could further reduce inflammation and tissue damage. However, whether and how PF affects macrophages activities in vitro remains unknown. In current study, using M1 and M2 cells generated from mouse bone marrow precursors, we explored the role of PF in regulating M1/M2 cells activity in vitro. The results showed that PF inhibited LPS-induced M1 activity by reducing iNOS expression and NO production via decreasing LPS/NF-κB signaling pathway; whereas, PF enhanced IL-4-provoked M2 function by up-regulating Arg-1 production and activity via increasing IL-4/STAT6 signaling pathway. Our new finding indicates that PF can suppress M1 cells activity and enhance M2 cells function simultaneously, which could help to ameliorate autoimmune and autoinflammatory diseases in clinical treatment.
巨噬细胞分为M1“促炎”巨噬细胞和M2“抗炎”巨噬细胞,且巨噬细胞极化失控在不同疾病的发病机制中起重要作用,这一观点已被广泛接受。作为白芍总苷的主要成分,芍药苷(PF)多年来一直被广泛用于治疗自身免疫性疾病和自身炎症性疾病。从机制上讲,已发现PF可改变多种免疫细胞的活性,进而减轻炎症和组织损伤。然而,PF在体外是否以及如何影响巨噬细胞活性仍不清楚。在当前研究中,我们使用从小鼠骨髓前体细胞生成的M1和M2细胞,探讨了PF在体外调节M1/M2细胞活性中的作用。结果表明,PF通过降低LPS/NF-κB信号通路,减少iNOS表达和NO生成,从而抑制LPS诱导的M1活性;而PF通过增加IL-4/STAT6信号通路,上调Arg-1的生成和活性,增强IL-4诱导的M2功能。我们的新发现表明,PF可同时抑制M1细胞活性并增强M2细胞功能,这可能有助于在临床治疗中改善自身免疫性疾病和自身炎症性疾病。