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蛇床子素通过抑制NF-κB/MIF信号通路减轻实验性哮喘中的巨噬细胞活化。

Osthole Attenuates Macrophage Activation in Experimental Asthma by Inhibitingthe NF-ĸB/MIF Signaling Pathway.

作者信息

Li Ruyi, Song Peng, Tang Guofang, Wei Jianghong, Rao Lizong, Ma Libing, Jiang Ming, Huang Jianwei, Xu Qing, Wu Jingjie, Lv Qian, Yao Dong, Xiao Bo, Huang Haiming, Lei Liping, Feng Juntao, Mo Biwen

机构信息

Key Laboratory of National Clinical Research Center for Respiratory Disease, Department of Respiratory and Critical Care Medicine, Xiangya Hospital, Central South University, Changsha, China.

Key Laboratory of Prevention and Treatment for Chronic Diseases by Traditional Chinese Medicine, Affiliated Hospital of Gansu University of Chinese Medicine, Lanzhou, China.

出版信息

Front Pharmacol. 2021 Mar 22;12:572463. doi: 10.3389/fphar.2021.572463. eCollection 2021.

Abstract

Inhibition of activated macrophages is an alternative therapeutic strategy for asthma. We investigated whether a coumarin compound, osthole, isolated from (L.) Cuss, alleviated macrophage activation and . Osthole could reduce expression of a marker of activated macrophages, cluster of differentiation (CD)206, in an ovalbumin-challenge model of asthma in mice. Osthole could also inhibit infiltration of inflammatory cells, collagen deposition and production of proinflammatory cytokines [interleukin (IL)-1β, tumor necrosis factor-ɑ, macrophage migration inhibitory factor (MIF)] in asthmatic mice. , expression of phosphorylated-IĸBɑ, MIF and M2 cytokines (Ym-1, Fizz-1, arginase-1) in IL-4-induced macrophages decreased upon exposure to the NF-ĸB inhibitor MG-132. In our short hairpin (sh)RNA-MIF-knockdown model, reduced expression of M2 cytokines was detected in the IL-4 + shRNA-MIF group. Osthole could attenuate the proliferation and migration of an IL-4-induced rat alveolar macrophages line (NR8383). Osthole could reduce IL-4-induced translocation of nuclear factor-kappa B (NF-ĸB) in NR8383 cells. Collectively, our results suggest that osthole ameliorates macrophage activation in asthma by suppressing the NF-ĸB/MIF signaling pathway, and might be a potential agent for treating asthma.

摘要

抑制活化的巨噬细胞是哮喘的一种替代治疗策略。我们研究了从蛇床(L.)Cuss中分离出的香豆素化合物蛇床子素是否能减轻巨噬细胞活化以及……。在小鼠哮喘卵清蛋白激发模型中,蛇床子素可降低活化巨噬细胞标志物分化簇(CD)206的表达。蛇床子素还可抑制哮喘小鼠中炎性细胞浸润、胶原沉积以及促炎细胞因子[白细胞介素(IL)-1β、肿瘤坏死因子-α、巨噬细胞迁移抑制因子(MIF)]的产生。……,在IL-4诱导的巨噬细胞中,暴露于NF-κB抑制剂MG-132后,磷酸化-IκBα、MIF和M2细胞因子(Ym-1、Fizz-1、精氨酸酶-1)的表达降低。在我们的短发夹(sh)RNA-MIF敲低模型中,在IL-4 + shRNA-MIF组中检测到M2细胞因子表达降低。蛇床子素可减弱IL-4诱导的大鼠肺泡巨噬细胞系(NR8383)的增殖和迁移。蛇床子素可减少IL-4诱导的NR8383细胞中核因子-κB(NF-κB)的转位。总体而言,我们的结果表明,蛇床子素通过抑制NF-κB/MIF信号通路改善哮喘中的巨噬细胞活化,可能是治疗哮喘的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f70/8020258/f29a69030d15/fphar-12-572463-g001.jpg

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