赵芳哲, 桑晓青, 朱彦, 杨剑. M2型巨噬细胞促分泌的IL-6因子对成纤维细胞活化的作用机制研究J. 药学学报, 2020,55(5): 892-897. doi: 10.16438/j.0513-4870.2019-1044
引用本文: 赵芳哲, 桑晓青, 朱彦, 杨剑. M2型巨噬细胞促分泌的IL-6因子对成纤维细胞活化的作用机制研究J. 药学学报, 2020,55(5): 892-897. doi: 10.16438/j.0513-4870.2019-1044
ZHAO Fang-zhe, SANG Xiao-qing, ZHU Yan, YANG Jian. Effect and mechanism of IL-6 induced by M2 macrophages on the lung fibroblasts activationJ. Acta Pharmaceutica Sinica, 2020,55(5): 892-897. doi: 10.16438/j.0513-4870.2019-1044
Citation: ZHAO Fang-zhe, SANG Xiao-qing, ZHU Yan, YANG Jian. Effect and mechanism of IL-6 induced by M2 macrophages on the lung fibroblasts activationJ. Acta Pharmaceutica Sinica, 2020,55(5): 892-897. doi: 10.16438/j.0513-4870.2019-1044

M2型巨噬细胞促分泌的IL-6因子对成纤维细胞活化的作用机制研究

Effect and mechanism of IL-6 induced by M2 macrophages on the lung fibroblasts activation

  • 摘要: 特发性肺纤维化(idiopathic pulmonary fibrosis,IPF)通常伴有炎症反应,其中巨噬细胞与其密切相关,通过巨噬细胞与肺成纤维细胞共培养模型和博来霉素诱导的IPF小鼠模型,本文探究了巨噬细胞和白细胞介素-6(interleukin 6,IL-6)与IPF的联系。动物福利和实验过程均遵循天津中医药大学动物伦理委员会的规定。结果表明,博来霉素(bleomycin,BLM)诱导的IPF小鼠体内IL-6含量明显升高,且肺部有大量的炎性细胞浸润。划痕及免疫荧光实验结果表明,共培养36 h替代活化型(alternatively activated,M2)巨噬细胞可诱导成纤维细胞迁移及活化,且在共培养体系中IL-6的表达随之增多。划痕及天狼星红实验结果证明IL-6可促进成纤维细胞迁移和活化。研究结果证明,M2型巨噬细胞通过促进成纤维细胞分泌IL-6,从而诱导成纤维细胞活化及迁移,影响IPF发展。

     

    Abstract: Idiopathic pulmonary fibrosis (IPF) is usually accompanied with inflammatory response, especially the macrophages. The co-culture model of macrophages and fibroblast, and IPF mice model induced by bleomycin were used here to explore the role of macrophages and interleukin-6 (IL-6) in IPF. All animals welfare and experiments were performed following the regulations of the Animal Ethics Committee of Tianjin University of Traditional Chinese Medicine. The results showed that the content of IL-6 in IPF mice induced by bleomycin was significantly increased, and there was a large amount of inflammatory cell infiltration in the lungs. The results of wound-healing and immunofluorescence showed that alternative activated (M2) macrophages could induce the migration and activation of fibroblasts at 36 h, and the expression of IL-6 was increased in the co-culture system. The results of wound-healing and sirius red assay proved that IL-6 could induce the migration and activation of fibroblast. The results showed that M2 macrophages induced fibroblasts to secrete IL-6, thereby inducing the activation and migration of fibroblast, which affect the development of IPF.

     

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