首页 | 本学科首页   官方微博 | 高级检索  
     

Akt激酶抑制剂MK-2206诱导U2OS人骨肉瘤细胞凋亡与自噬
引用本文:王雪莹,李照梅,周运生,郭文莉,王凤泽. Akt激酶抑制剂MK-2206诱导U2OS人骨肉瘤细胞凋亡与自噬[J]. 中国病理生理杂志, 2014, 30(9): 1580-1583. DOI: 10.3969/j.issn.1000-4718.2014.09.007
作者姓名:王雪莹  李照梅  周运生  郭文莉  王凤泽
作者单位:1泰山医学院生物科学学院,山东 泰安 271016; 2泰安市中心医院放疗中心,山东 泰安 271000;3淄博市博山区疾病预防控制中心,山东 淄博 255200
基金项目:国家自然科学基金资助项目(No.81272683);山东省自然科学基金资助项目(No.ZR2011HQ034)
摘    要: 目的:研究Akt抑制剂MK-2206对U2OS细胞凋亡和自噬的影响。方法:采用MTT法检测MK-2206对U2OS细胞活力的影响,DNA片段末端标记试剂盒检测细胞凋亡的变化,免疫印迹法检测细胞内蛋白的表达,用LC3-II的表达量用来确定细胞的自噬水平。结果:MK-2206剂量依赖性地降低了U2OS细胞的活力;MK-2206能够促进caspase-9、caspase-3和PARP的活化切割而诱导U2OS细胞发生凋亡;MK-2206给药后可促进细胞内LC3-II的表达,氯喹阻断自噬后明显增强了MK-2206对U2OS细胞活力的抑制作用。结论:Akt 抑制剂MK-2206能够诱导U2OS细胞发生凋亡和自噬;抑制自噬可促进MK-2206对U2OS细胞的毒性。

关 键 词:MK-2206  细胞凋亡  细胞自噬  U2OS细胞  
收稿时间:2014-04-01

MK-2206, an inhibitor of Akt,induced cell apoptosis and autophagy in U2OS cells
WANG Xue-ying,LI Zhao-mei,ZHOU Yun-sheng,GUO Wen-li,WANG Feng-ze. MK-2206, an inhibitor of Akt,induced cell apoptosis and autophagy in U2OS cells[J]. Chinese Journal of Pathophysiology, 2014, 30(9): 1580-1583. DOI: 10.3969/j.issn.1000-4718.2014.09.007
Authors:WANG Xue-ying  LI Zhao-mei  ZHOU Yun-sheng  GUO Wen-li  WANG Feng-ze
Affiliation:1School of Biological Science, Taishan Medical College, Taian 271016, China; 2Department of Radiation Oncology, Central Hospital of Taian, Taian 271000, China; 3The Center for Disease Control and Prevention of Boshan District, Zibo 255200, China.
Abstract:AIM:To observe the effect of MK-2206, an inhibitor of Akt, on the cell apoptosis and autophagy of U2OS cells. METHODS:The cell viability was detected by MTT assay. The cell apoptosis was analyzed by TdT-mediated dUTP nick end labeling assay. The expression of LC3-II was examined by Western blotting. RESULTS:MK-2206 inhibited the cell viability in a dose-dependent manner. MK-2206 induced the cell apoptosis via activation of caspase-3, caspase-9 and PARP. MK-2206 treatment substantially induced the U2OS cell autophagy by increasing in the levels of LC3-II. Blockage of autophagy using chloroquine magnified MK-2206-induced cell death in U2OS cells. CONCLUSION:The Akt inhibitor MK-2206 induces cell apoptosis and autophagy. Blocking autophagy magnifies MK-2206-induced the inhibition of the viability in U2OS cells.
Keywords:MK-2206   Apoptosis  Cell autophagy  U2OS cells
点击此处可从《中国病理生理杂志》浏览原始摘要信息
点击此处可从《中国病理生理杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号