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作 者:任姸 曹留霞 张静[1] 刘晓萍[1] 卞晶晶[1] 陈琛[1]
机构地区:[1]青岛大学医学院组织胚胎学教研室,山东青岛266021
出 处:《齐鲁医学杂志》2014年第4期286-288,292,共4页Medical Journal of Qilu
基 金:山东省自然科学基金资助项目(ZR2012CM008)
摘 要:目的观察诱导型一氧化氮合酶(iNOs)在表没食子儿茶素没食子酸酯(EGCG)促A549细胞凋亡中的作用。方法体外培养A549细胞,随机分为对照组、EGCG组,MTT方法检测筛选EGCG最佳作用浓度,流式细胞仪检测EGCG促A549细胞凋亡作用,免疫组化染色法、蛋白质印迹定量分析法与Real time—PCR方法检测各组中iNOS蛋白和mRNA的表达情况。结果200mg/L的EGCG组细胞增殖活性与其他组比较差异有显著意义(F—1000.35,q=3.43~60.00,P〈0.05)。EGCG组晚期A549细胞凋亡率与对照组比较,差异有显著性(x2 =65.23,P〈0.05)。与对照组比较,EGCG同样可以降低A549细胞中iNOS蛋白与mRNA的表达量,差异有显著性(t=9.4、5.7,P〈0.05)。结论EGCG促A549细胞凋亡可能与下调iNOS蛋白与mRNA的表达量有关。Objective To investigate the effect of inducible NOS (iNOS) on EGCG promoting apoptosis of A549 cells. Methods A549 cells were cultured in vitro and randomized to two groups: control group and model group. Optimal concentration of EGCG was obtained by MTT assay. The apoptosis effect of EGCG on A549 cells was detected by flow cytometry. The expres- sions of iNOS and mRNA were detected by immunocytochemical western blotting and real fime-PCR. Results The results showed that the differences of cell proliferation activity between 200 mg/L EGCG group and other groups were significant (F : 1 000.35,q = 3.43-60.00, P 〈 0.05). The differences of the apoptosis rate of advanced stage A549 cells between EGCG group and the control were significant (x2=65.23,P〈0.05). Compared with the control group, EGCG could also reduce the expressions of iNOS protein and mRNA in A549 cells (t=9.4,5.7;P〈0.05). Conclusion The apoptosis activity of A549 cells treated with EGCG is likely to be related with downregulation of the expressions of iNOS protein and mRNA.
关 键 词:表没食子儿茶素没食子酸酯 一氧化氮合酶 细胞凋亡
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