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作 者:邓霞[1] 郑丹丹[1] 庄琼馨 柳星星 钱粉红[1] DENG Xia ZHENG Dan-dan ZHUANG Qiong-xin LIU Xing-xing QIAN Fen-hong(Department of Respiratory Medicine, the Affiliated Hospital of Jiangsu University, Zhenjiang Jiangsu 212001, China)
机构地区:[1]江苏大学附属医院呼吸内科,江苏镇江212001
出 处:《江苏大学学报(医学版)》2017年第2期123-127,共5页Journal of Jiangsu University:Medicine Edition
基 金:国家自然科学基金资助项目(81370119);镇江市社会发展项目(SH2015044)
摘 要:目的:探究虫草素对支气管上皮细胞炎症反应的调节作用及其机制。方法:培养人支气管上皮细胞系(16HBE),选择状态良好的16HBE细胞分别用不同浓度的虫草素(0、10、20、40、60μmol/m L)处理4 h后,脂多糖(1mg/L)处理12 h,MTT法检测细胞存活力;采用荧光定量PCR检测炎症细胞因子IL-8、TNF-α的mRNA相对表达水平;蛋白质印迹法检测p-AKT2、AKT2的蛋白表达水平。结果:虫草素能以剂量依赖的方式提高细胞存活力(P<0.05),抑制脂多糖诱导的IL-8、TNF-α的mRNA相对表达量(P<0.05),减少脂多糖活化的p-AKT2水平(P<0.05)。结论:虫草素在减弱脂多糖诱导的支气管上皮细胞炎症反应中起重要作用,其机制可能涉及AKT2信号通路的下调。Objective:To investigate the role of cordycepin in regulating the inflammatory response of human bronchial epithelial cells and its underlying mechanism.Methods:The human bronchial epithelial cells(16HBE),which grew in good condition,were treated with different concentrations of cordycepin(0,10,20,40,60 μmol/m L) for 4 hours and then treated with lipopolysaccharide(LPS,1 mg/L) for 12 hours.MTT assay was used for the detection of cell vitality.At the same time,the mRNA expression level of inflammatory cytokines(IL-8,TNF-α) was evaluated by quantitative real-time PCR.The level of pAKT2 expression was analyzed by Western blotting analysis.Results:Cordycepin could protect bronchial epithelial cells from damage of LPS in a concentration-dependent manner(P 0.05),and attenuated LPSinduced release of pro-inflammatory cytokines(P 0.05),down-regulate the phosphorylation level of AKT2 induced by LPS(P 0.05).Conclusion:Cordycepin shows active inhibitory effect on the inflammatory response of 16 HBE cells,possibly through mediating relevant signal pathway of AKT2.
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