Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, China.
Zhejiang Provincial Engineering Technology Research Center of Marine Biomedical Products, School of Food and Pharmacy, Zhejiang Ocean University, Zhoushan 316022, China.
Molecules. 2019 May 7;24(9):1766. doi: 10.3390/molecules24091766.
PM is particulate matter with a diameter of 2.5 μm or less. Airway macrophages are the key players regulating PM-induced inflammation. High molecular weight hyaluronan (HMW-HA) has previously been shown to exert protective effects on PM-induced acute lung injury and inflammation. However, little is known about the detailed mechanism. In this study, we aimed to determine whether HMW-HA alleviates PM-induced pulmonary inflammation by modulating macrophage polarization. The levels of M1 biomarkers TNF-α, IL-1β, IL-6, CXCL1, CXCL2, NOS2 and CD86, as well as M2 biomarkers IL-10, MRC1, and Arg-1 produced by macrophages were measured by ELISA, qPCR, and flow cytometry. In addition, the amount of M1 macrophages in lung tissues was examined by immunofluorescence of CD68 and NOS2. We observed a decline in PM-induced M1 polarization both in macrophages and lung tissues when HMW-HA was administered simultaneously. Meanwhile, western blot analysis revealed that PM-induced JNK and p38 phosphorylation was suppressed by HMW-HA. Furthermore, in vitro and in vivo studies showed that co-stimulation with HMW-HA and PM promoted the expression and release of IL-10, but exhibited limited effects on the transcription of MRC1 and ARG1. In conclusion, our results demonstrated that HMW-HA ameliorates PM-induced lung inflammation by repressing M1 polarization through JNK and p38 pathways and promoting the production of pro-resolving cytokine IL-10.
PM 是指直径为 2.5μm 或以下的颗粒物。气道巨噬细胞是调节 PM 诱导炎症的关键细胞。高分子量透明质酸(HMW-HA)先前已被证明对 PM 诱导的急性肺损伤和炎症具有保护作用。然而,其详细机制尚不清楚。在这项研究中,我们旨在确定 HMW-HA 是否通过调节巨噬细胞极化来减轻 PM 诱导的肺部炎症。通过 ELISA、qPCR 和流式细胞术测量巨噬细胞产生的 M1 生物标志物 TNF-α、IL-1β、IL-6、CXCL1、CXCL2、NOS2 和 CD86 以及 M2 生物标志物 IL-10、MRC1 和 Arg-1 的水平。此外,通过 CD68 和 NOS2 的免疫荧光检测肺组织中 M1 巨噬细胞的数量。当同时给予 HMW-HA 时,我们观察到 PM 诱导的 M1 极化在巨噬细胞和肺组织中均下降。同时,Western blot 分析表明 HMW-HA 抑制了 PM 诱导的 JNK 和 p38 磷酸化。此外,体内外研究表明,HMW-HA 和 PM 的共同刺激促进了 IL-10 的表达和释放,但对 MRC1 和 ARG1 的转录作用有限。总之,我们的结果表明,HMW-HA 通过 JNK 和 p38 通路抑制 M1 极化并促进抗炎细胞因子 IL-10 的产生,从而改善 PM 诱导的肺部炎症。