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Mechanisms Underlying Apoptosis-Inducing Effects of Kaempferol in HT-29 Human Colon Cancer Cells

机译:山萘酚在HT-29人结肠癌细胞中诱导凋亡的机制。

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We previously noted that kaempferol, a flavonol present in vegetables and fruits, reduced cell cycle progression of HT-29 cells. To examine whether kaempferol induces apoptosis of HT-29 cells and to explore the underlying molecular mechanisms, cells were treated with various concentrations (0–60 μmol/L) of kaempferol and analyzed by Hoechst staining, Annexin V staining, JC-1 labeling of the mitochondria, immunoprecipitation, in vitro kinase assays, Western blot analyses, and caspase-8 assays. Kaempferol increased chromatin condensation, DNA fragmentation and the number of early apoptotic cells in HT-29 cells in a dose-dependent manner. In addition, kaempferol increased the levels of cleaved caspase-9, caspase-3 and caspase-7 as well as those of cleaved poly (ADP-ribose) polymerase. Moreover, it increased mitochondrial membrane permeability and cytosolic cytochrome c concentrations. Further, kaempferol decreased the levels of Bcl-xL proteins, but increased those of Bik. It also induced a reduction in Akt activation and Akt activity and an increase in mitochondrial Bad. Additionally, kaempferol increased the levels of membrane-bound FAS ligand, decreased those of uncleaved caspase-8 and intact Bid and increased caspase-8 activity. These results indicate that kaempferol induces the apoptosis of HT-29 cells via events associated with the activation of cell surface death receptors and the mitochondrial pathway.
机译:我们先前注意到,山emp酚(一种存在于蔬菜和水果中的黄酮醇)减少了HT-29细胞的细胞周期进程。为了检查山emp酚是否诱导HT-29细胞凋亡并探讨其潜在的分子机制,将细胞用不同浓度(0-60μmol/ L)的山emp酚处理,并通过Hoechst染色,Annexin V染色,JC-1标记进行分析。线粒体,免疫沉淀,体外激酶测定,蛋白质印迹分析和caspase-8测定。山emp酚以剂量依赖性方式增加了HT-29细胞中的染色质浓缩,DNA片段化和早期凋亡细胞的数量。此外,山emp酚可增加裂解的caspase-9,caspase-3和caspase-7以及裂解的多聚(ADP-核糖)聚合酶的水平。而且,它增加了线粒体膜的通透性和胞质细胞色素c的浓度。此外,山奈酚降低了Bcl-xL蛋白的水平,但增加了Bik的水平。它还诱导了Akt活化和Akt活性的降低以及线粒体Bad的升高。此外,山奈酚增加了膜结合的FAS配体的水平,降低了未切割的caspase-8和完整Bid的水平,并提高了caspase-8的活性。这些结果表明山emp酚通过与细胞表面死亡受体和线粒体途径的活化有关的事件诱导HT-29细胞的凋亡。

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