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作 者:张东芳[1] 肖鹏[1] 韩晨露[1] 李卫国[1] 王坤英[1]
机构地区:[1]河南师范大学生命科学学院,河南新乡453007
出 处:《中国生物化学与分子生物学报》2014年第4期402-408,共7页Chinese Journal of Biochemistry and Molecular Biology
基 金:河南省重点科技攻关计划(No.122102310282);河南省教育厅自然科学基础研究计划(No.2010A180011)~~
摘 要:表没食子儿茶素-3-没食子酸酯(epigallocatechin-3-gallate,EGCG)具有抗氧化、抗癌、抗炎等多种生物学特性,但对巨噬细胞中表达TNF-α及IL-1β的报告尚存在争议.本文旨在探索EGCG对脂多糖(LPS)诱导的小鼠腹腔巨噬细胞和RAW264-7细胞促炎细胞因子Tnf-α和Il-1β基因表达的影响.MTT结果显示,0-100μmol/LEGCG对RAW264.7细胞活力没有影响;实时荧光定量PCR(qRT-PCR)和ELISA分析显示,1ing/LLPS可显著升高小鼠腹腔巨噬细胞和RAW264.7细胞Tnf-α和Il-1βmRNA和蛋白水平,EGCG单独处理对巨噬细胞Tnfα和Il-1β的基因表达与蛋白生成没有影响,但可以抑制LPS诱导的巨噬细胞Tnf-α和Il-1β的基因表达与蛋白生成,并存在剂量依赖效应.上述结果提示,EGCG可以剂量依赖方式抑制LPS诱导的巨噬细胞促炎细胞因子Tnf-α和Il-1β的表达,这可能与EGCG的抗炎效应有关.Epigallocatechin-3-gallate (EGCG) has various pharmacological activities, including anticancer, anti-oxidative and anti-inflammatory effects. However, whether EGCG affects the expression of proinflammatory cytokines of Tnf-α and II-1β in macrophage is still in dispute. This study aimed to characterize the effect of EGCG on lipopolysaccharide (LPS)-induced Tnf-α and II-1β expression in murine peritoneal and RAW264.7 macrophages. The MTT results showed that EGCG did not exert cytotoxicity at tested concentrations of 0 - 100 results showed that 1 mg/L LPS stimulated the μmol/L in RAW264.7 cells. The qRT-PCR and ELISA mRNA and protein levels of Tnf-α and Il-1β, but not EGCG treatment alone. In fact, EGCG inhibited LPS-induced Tnf-α and Il-1β expression and protein secretion in a dose-dependent manner. Our results suggested that EGCG inhibited LPS-induced pro inflammatory gene expression for its anti-inflammatory effects.
关 键 词:表没食子儿茶素-3-没食子酸酯 脂多糖 巨噬细胞 肿瘤坏死因子-α 白介素-1Β
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