引用本文
  • 萧文泽,赵力,邹和建.白藜芦醇促进巨噬细胞M2极化并缓解小鼠急性痛风性关节炎[J].第二军医大学学报,2019,40(8):860-865    [点击复制]
  • XIAO Wen-ze,ZHAO Li,ZOU He-jian.Resveratrol promotes macrophage M2 polarization and alleviates acute gouty arthritis in mice[J].Acad J Sec Mil Med Univ,2019,40(8):860-865   [点击复制]
【打印本页】 【下载PDF全文】 【HTML】 查看/发表评论下载PDF阅读器关闭

←前一篇|后一篇→

过刊浏览    高级检索

本文已被:浏览 149次   下载 110 本文二维码信息
码上扫一扫!
白藜芦醇促进巨噬细胞M2极化并缓解小鼠急性痛风性关节炎
萧文泽1,2,赵力2,邹和建2*
0
(1. 复旦大学附属浦东医院内分泌免疫科, 上海 201399;
2. 复旦大学附属华山医院风湿免疫科, 上海 200040
*通信作者)
摘要:
目的 观察白藜芦醇对小鼠急性痛风性关节炎的预防效果,并探讨巨噬细胞M2极化是否介导白藜芦醇的作用。方法 18只C57BL/6小鼠随机分为3组,每组6只:假手术组、造模+溶剂对照组、造模+白藜芦醇组。假手术组用无菌生理盐水处理小鼠右侧后肢踝关节,造模+溶剂对照组小鼠右侧后肢踝关节给予单钠尿酸盐(MSU)晶体构建急性痛风性关节炎模型,造模+白藜芦醇组提前给予DMSO溶解的白藜芦醇干预再进行MSU晶体造模。测定各组小鼠双侧足掌厚度,采用H-E染色观察各组小鼠足掌关节滑膜组织炎症情况。分离、提取正常小鼠腹腔原代巨噬细胞,给予白藜芦醇干预后以MSU晶体刺激,用蛋白质印迹法检测巨噬细胞M1极化标志物诱导型一氧化氮合酶(iNOS)的表达,用实时荧光定量PCR检测巨噬细胞中炎症指标肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β)mRNA的表达水平,用流式细胞术检测M2型巨噬细胞标志物F4/80、CD163的表达。结果 成功构建小鼠急性痛风性关节炎模型。造模前给予白藜芦醇干预后,小鼠右侧后肢足掌厚度明显低于溶剂对照组[(1.98±0.02)mm vs(2.49±0.12)mm,P<0.01],小鼠足掌关节炎滑膜组织中中性粒细胞浸润面积减少。体外实验中,白藜芦醇显著抑制了小鼠腹腔原代巨噬细胞中iNOS蛋白和TNF-αIL-1β mRNA的表达水平(P均<0.01),提高了F4/80+CD163+细胞比例(P<0.01)。结论 白藜芦醇可能通过促进巨噬细胞M2极化,抑制炎性因子的产生,从而有效缓解小鼠急性痛风性关节炎。
关键词:  白藜芦醇  痛风性关节炎  巨噬细胞极化  肿瘤坏死因子α  白细胞介素1β
DOI:10.16781/j.0258-879x.2019.08.0860
投稿时间:2019-06-12修订日期:2019-07-07
基金项目:国家自然科学基金(8167060028),浦东新区科技发展基金(PKJ2018-Y36),复旦大学浦东医院浦菁人才培养计划(PJ201502).
Resveratrol promotes macrophage M2 polarization and alleviates acute gouty arthritis in mice
XIAO Wen-ze1,2,ZHAO Li2,ZOU He-jian2*
(1. Department of Endocrine and Immunology, Shanghai Pudong Hospital, Fudan University, Shanghai 201399, China;
2. Department of Rheumatology and Immunology, Huashan Hospital, Fudan University, Shanghai 200040, China
*Corresponding author)
Abstract:
Objective To investigate the preventive effect of resveratrol against acute gouty arthritis in mice and whether M2 polarization of macrophage mediates the effect. Methods Eighteen C57BL/6 mice were randomly divided into three groups (n=6):sham group, model+solvent control group, and model+resveratrol group. The right hind limb ankle joint of mice in the sham group were treated with sterile normal saline. The right hind limb ankle joint of mice in the model+solvent control group were treated with DMSO in advance and then with monosodium urate (MSU) crystals to establish acute gouty arthritis model. Mice in the model+resveratrol group were treated with resveratrol dissolved in DMSO in advance and then with MSU crystals to establish acute gouty arthritis model. The bilateral paw thickness of mice in each group was measured and H-E staining was used to observe the inflammation of synovial tissue of feet and metacarpal joints of mice in each group. The primary macrophages from abdominal cavity of normal mice were extracted, treated with resveratrol, and then stimulated with MSU crystals. The expression of M1-polarized macrophage markers inducible nitric oxide synthase (iNOS) protein and the inflammatory indexes tumor necrosis factor α (TNF-α) mRNA and interleukin 1β (IL-1β) mRNA were detected by Western blotting or qPCR. The expression of M2-polarized macrophage markers F4/80 and CD163 were detected by flow cytometry. Results Acute gouty arthritis model of mice was successfully established. The right hind limb thickness of mice in the model+resveratrol group was significantly lower than that in the model+solvent control group ([1.98±0.02] mm vs[2.49±0.12] mm, P<0.01). The infiltration area of neutrophils in synovial tissue of feet and metacarpal joints in mice of model+resveratrol group were also significantly reduced. In vitro, resveratrol significantly inhibited the expression of iNOS protein, TNF-α mRNA and IL-1β mRNA in primary peritoneal macrophages (all P<0.01) and increased the percentage of F4/80+CD163+ in macrophages (P<0.01). Conclusion Resveratrol may effectively alleviate acute gouty arthritis in mice by promoting M2 polarization of macrophages and inhibiting the expression of inflammatory factors.
Key words:  resveratrol  gouty arthritis  macrophage polarization  tumor necrosis factor α  interleukin 1β