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EGCG对A549细胞炎性反应模型UBC9表达的影响
引用本文:曹留霞,武涧松,徐晓丹,贺丹.EGCG对A549细胞炎性反应模型UBC9表达的影响[J].武警医学,2017,28(3):235-239.
作者姓名:曹留霞  武涧松  徐晓丹  贺丹
作者单位:100088 北京,火箭军总医院感染性疾病科
基金项目:山东省自然科学基金资助课题(ZR2012CM008)
摘    要: 目的 观察泛素连接酶9(ubiquitin conjugating enzyme 9,UBC9)在表没食子儿茶素没食子酸酯(epigallocatechin-3-gallate,EGCG)作用的脂多糖(lipopolysaccharide,LPS)诱导A549细胞中的表达,探讨UBC9与EGCG抗炎性反应机制的相关性。方法 根据筛选结果随机分为对照组、EGCG组、LPS组、EGCG+LPS组4个组,MTT检测不同浓度的EGCG(50~400 μg/ml)和LPS(10~50 μg/ml)对A549细胞增殖活性的影响,筛选最佳作用浓度,进一步通过免疫组化染色法、蛋白质印迹法和Realtime-PCR检测分析各处理组UBC9蛋白及其mRNA的相对表达量。结果 MTT显示,200 μg/ml的EGCG细胞增殖抑制作用最强(F=1618.18,P<0.001),LPS 25μg/ml细胞增殖活性最明显(F=237.38,P<0.001)。免疫组化与蛋白质印迹检测均显示,与对照组比较,EGCG下调A549细胞UBC9蛋白表达(P<0.001),LPS则上调UBC9表达量(P<0.001),与LPS组比较,EGCG+LPS组UBC9蛋白表达明显降低(P<0.001)。同样,Realtime-PCR显示,与对照组比较,EGCG组UBC9 mRNA表达下调(F=89.34,P<0.001),LPS组UBC9 mRNA表达上调(F=225.00,P<0.001),与LPS组比较,EGCG+LPS组UBC9 mRNA的表达受到抑制,显著降低(F=625.00,P<0.001)。结论 EGCG下调LPS刺激的炎性反应模型的UBC9的表达,其抗炎机制可能与抑制UBC9蛋白与mRNA表达有关。

关 键 词:表没食子儿茶素没食子酸酯    脂多糖    泛素连接酶9    炎性反应  
收稿时间:2016-09-05

Effect of EGCG on UBC9 expression in inflammatory model of A549 cells
CAO Liuxia,WU Jiansong,XU Xiaodan,HE Dan.Effect of EGCG on UBC9 expression in inflammatory model of A549 cells[J].Medical Journal of the Chinese People's Armed Police Forces,2017,28(3):235-239.
Authors:CAO Liuxia  WU Jiansong  XU Xiaodan  HE Dan
Affiliation:Department of Infectious Diseases, General Hospital of the PLA Rocket Force, Beijing 100088, China
Abstract:Objective To observe the effect of EGCG on the expression of UBC9 in the A549 inflammatory model,and investigate its correlation with the anti-inflammatory mechanism of EGCG.Methods A549 cells were randomly divided in vitro into four group:control group,EGCG group,LPS group,and EGCG plus LPS group.The proliferative activity of A549 cells,which were incubated with different concentrations of EGCG(50 ~400 μg/ml) and LPS(10 ~50 μg/ml),was detected by MTT method to select the optimum concentration for experiment.The relative expressions of UBC9 protein and mRNA in each group were determined with immunohistochemical staining,Western blot and real-time-PCR,and compared.Results MTT showed that 200 μg/ml EGCG had the strongest inhibitory effect on proliferation of A549 cells(F =16181.18,P <0.001),while 25 μg/ml LPS had the strongest promoting effect (F =237.38,P < 0.001).As observed with immunohistochemistry and Western blot,EGCG down-regulated the expression of UBC9 protein(P <0.001) while LPS up-regulated the expression(P < 0.001) compared to control group.Compared to LPS group,the expression of UBC9 protein in EGCG plus LPS group was reduced significantly(P < 0.001).Similarly,Real-time-PCR revealed that the expression of UBC9 mRNA decreased in EGCG group(F =89.34,P <0.001),but increased in LPS group(F =225.00,P <0.001) compared with control group.Compared to LPS group,the expression of UBC9 mRNA in EGCG plus LPS group was inhibited and reduced significantly(F =625.00,P < 0.001).Conclusions EGCG can down-regulate the expression of UBC9 in the inflammatory model induced by LPS.The anti-inflammatory mechanism of EGCG might be mediated by suppression of UBC9 protein and mRNA expression.
Keywords:epigallocatechin gallate  lipopolysaccharide  ubiquitin-conjugating enzyme 9  inflammation
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