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作 者:李亚秋[1] 苏晓薇[2] 黄孙卉[1] 许冬明[1] 郝嘉南[1] 郝利铭[2] LI Ya-qiu SU Xiao-wei HUANG Sun-hui XU Dong-ming HAO Jia-nan HAO Li-ming(Department of Anatomy,Jilin Medical College,Jilin 132013,China School of Basic Medical Sciences,Jilin University,Changchun 130021 ,China)
机构地区:[1]吉林医药学院解剖教研室,吉林吉林132013 [2]吉林大学基础医学院,吉林长春130021
出 处:《东北师大学报(自然科学版)》2016年第4期116-120,共5页Journal of Northeast Normal University(Natural Science Edition)
基 金:吉林省科技发展计划项目(20100920)
摘 要:采用常规培养肺腺癌细胞Calu-3的方法,利用MTT和CCK-8法确定囊性纤维化跨膜传导调节因子(cystic fibrosis transmembrane conductance regulator,CFTR)的激活剂(Genistein)和抑制剂(CFTRinh-172)的最适浓度,用CFTR激活剂和抑制剂的最佳浓度分别处理Calu-3细胞,然后采用划痕实验观测了培养48h后Calu-3细胞迁移的差异.结果表明:MTT法检测激活剂的最佳浓度为25μmol/L;CCK-8法检测抑制剂的最佳浓度为10μmol/L;划痕实验检测得出25μmol/L激活剂组细胞迁移数量((74.2±5.79)个)与对照组细胞迁移数量((134.1±10.04)个)相比具有显著性差异(P=0.00<0.01);10μmol/L抑制剂组细胞迁移数量((148.3±17.70)个)与对照组细胞迁移数量((134.1±10.04)个)相比无显著性差异(P=0.27>0.05).激活剂通过促进CFTR氯离子通道的开放,抑制了肺腺癌肿瘤细胞Calu-3的迁移.Calu-3 were cultured by conventional method in this paper,and the optimal concentrations of activator and inhibitor of cystic fibrosis transmembrane conductance regulator were determined by MTT and CCK-8 method,the optimal concentrations of the CFTR activator(Genistein) and inhibitor (CFTRinh-172) were added to the cell,detected the migration of cultured Calu3 cells by scratch test in 48 h. The following results were obtained:The optimal concentrations of activator were 25 μmol/L. The Optimal concentrations of inhibitor were 10μmol/L. The results of scratch tests showed that there was significant difference(P=0.00〈0.01) between the number of cell migration of activator(25 μmol/L) group(74.2±5.79) and the number of cell migration of control group(134.1 ±10.04). There was no significant difference(P=0.27〉0.05) between the number of cell migration of inhibitor(10 μmol/L) group and the number of cell migration of control group (134. 1 ±10. 04). Activator (Genistein) inhibited the migration of lung adenocarcinoma cells by making the CFTR chloride ion channels open.
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