中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
THE CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2015年
11期
932-934,959
,共4页
刘学军%黄赛瑜%高金建%凡启军%倪丽艳%陈波蓓
劉學軍%黃賽瑜%高金建%凡啟軍%倪麗豔%陳波蓓
류학군%황새유%고금건%범계군%예려염%진파배
吲哚-3-甲醇%人喉癌上皮细胞%细胞增殖%细胞凋亡
吲哚-3-甲醇%人喉癌上皮細胞%細胞增殖%細胞凋亡
신타-3-갑순%인후암상피세포%세포증식%세포조망
indole -3 -carbinol%Hep -2 cell%cell proliferation%cell apoptosis
目的:研究吲哚-3-甲醇对人喉癌上皮细胞( Hep-2)增殖及凋亡的影响。方法实验分为5组,4个浓度实验组(吲哚-3-甲醇,0,50,100,150μmol· L-1)与对照组(二甲基亚砜)。用水溶性四氮唑法检测吲哚-3-甲醇对Hep-2细胞增殖的影响,用Hochest33258染色及流式细胞仪检测吲哚-3-甲醇诱导的Hep-2细胞的凋亡,用蛋白免疫印迹方法检测凋亡相关信号分子livin蛋白表达情况。结果经4个浓度实验组及对照组处理48 h后,Hep-2细胞的凋亡率分别为(3.95±0.68)%,(8.54±1.35)%,(21.28±2.32)%,(38.65±4.85)%和(4.26±0.58)%。表明吲哚-3-甲醇以浓度依赖方式抑制Hep-2增殖,诱导细胞凋亡和Livin蛋白表达。结论吲哚-3-甲醇可抑制Hep-2细胞增殖,其诱导细胞凋亡可能与Livin蛋白表达的抑制相关。
目的:研究吲哚-3-甲醇對人喉癌上皮細胞( Hep-2)增殖及凋亡的影響。方法實驗分為5組,4箇濃度實驗組(吲哚-3-甲醇,0,50,100,150μmol· L-1)與對照組(二甲基亞砜)。用水溶性四氮唑法檢測吲哚-3-甲醇對Hep-2細胞增殖的影響,用Hochest33258染色及流式細胞儀檢測吲哚-3-甲醇誘導的Hep-2細胞的凋亡,用蛋白免疫印跡方法檢測凋亡相關信號分子livin蛋白錶達情況。結果經4箇濃度實驗組及對照組處理48 h後,Hep-2細胞的凋亡率分彆為(3.95±0.68)%,(8.54±1.35)%,(21.28±2.32)%,(38.65±4.85)%和(4.26±0.58)%。錶明吲哚-3-甲醇以濃度依賴方式抑製Hep-2增殖,誘導細胞凋亡和Livin蛋白錶達。結論吲哚-3-甲醇可抑製Hep-2細胞增殖,其誘導細胞凋亡可能與Livin蛋白錶達的抑製相關。
목적:연구신타-3-갑순대인후암상피세포( Hep-2)증식급조망적영향。방법실험분위5조,4개농도실험조(신타-3-갑순,0,50,100,150μmol· L-1)여대조조(이갑기아풍)。용수용성사담서법검측신타-3-갑순대Hep-2세포증식적영향,용Hochest33258염색급류식세포의검측신타-3-갑순유도적Hep-2세포적조망,용단백면역인적방법검측조망상관신호분자livin단백표체정황。결과경4개농도실험조급대조조처리48 h후,Hep-2세포적조망솔분별위(3.95±0.68)%,(8.54±1.35)%,(21.28±2.32)%,(38.65±4.85)%화(4.26±0.58)%。표명신타-3-갑순이농도의뢰방식억제Hep-2증식,유도세포조망화Livin단백표체。결론신타-3-갑순가억제Hep-2세포증식,기유도세포조망가능여Livin단백표체적억제상관。
Objective To study the effect of indoel -3 -carbinol on Hep-2 cells in vitro.Methods There was divided into 5 groups, the 4 test groups (the concerntration of indoel-3-carbinol, 0, 50, 100, 150μmol· L-1) and the control group(dimethyl sulfoxide).The inhibition of cell proliferation was assayed by method of WST-1.And the apopto-sis was shown with Hochest33258 staining and flow cytometry.The mechanism of apoptosis, and the expressions of the livin protein were detected by Western blotting assay.Results After being disposed by the test groups with 4 different concerntration of indoel-3-carbinol and the control group, the apoptosis rate of Hep-2 cells were(3.95 ±0.68)%, ( 8.54 ±1.35 )%, ( 21.28 ±2.32 )%, ( 38.65 ±4.85 )%, and (4.26 ±0.58)%, respectively.The indoel -3 -carbinol could inhibit the proliferation of Hep-2 cells with the dose-dependent manner and the apoptosis could be induced too.Furthermore, the expressions of Livin appeared to be decreased significantly as compared with the control group.Conclusion The indoel-3-carbinol could induce apoptosis of Hep-2 cells in the manner of dose-dependent, and Livin might play a role during above processes.