首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Proliferation-Attenuating and Apoptosis-Inducing Effects of Tryptanthrin on Human Chronic Myeloid Leukemia K562 Cell Line in Vitro
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Proliferation-Attenuating and Apoptosis-Inducing Effects of Tryptanthrin on Human Chronic Myeloid Leukemia K562 Cell Line in Vitro

机译:Tryptanthrin对人慢性粒细胞白血病K562细胞株的增殖抑制和凋亡诱导作用

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摘要

Tryptanthrin, a kind of indole quinazoline alkaloid, has been shown to exhibit anti-microbial, anti-inflammation and anti-tumor effects both in vivo and in vitro. However, its biological activity on human chronic myeloid leukemia cell line K562 is not fully understood. In the present study, we investigated the proliferation-attenuating and apoptosis-inducing effects of tryptanthrin on leukemia K562 cells in vitro and explored the underlying mechanisms. The results showed that tryptanthrin could significantly inhibit K562 cells proliferation in a time- and dose-dependent manner as evidenced by MTT assay and flow cytometry analysis. We also observed pyknosis, chromatin margination and the formation of apoptotic bodies in the presence of tryptanthrin under the electron microscope. Nuclei fragmentation and condensation by Hoechst 33258 staining were detected as well. The amount of apoptotic cells significantly increased whereas the mitochondrial membrane potential decreased dramatically after tryptanthrin exposure. K562 cells in the tryptanthrin treated group exhibited an increase in cytosol cyt-c, Bax and activated caspase-3 expression while a decrease in Bcl-2, mito cyt-c and pro-caspase-3 contents. However, the changes of pro-caspase-3 and activated caspase-3 could be abolished by a pan-caspase inhibitor ZVAD-FMK. These results suggest that tryptanthrin has proliferation-attenuating and apoptosis-inducing effects on K562 cells. The underlying mechanism is probably attributed to the reduction in mitochondria membrane potential, the release of mito cyt-c and pro-caspase-3 activation.
机译:Tryptanthrin是一种吲哚喹唑啉生物碱,在体内和体外均表现出抗微生物,抗发炎和抗肿瘤作用。然而,其对人慢性髓性白血病细胞系K562的生物学活性尚未完全了解。在本研究中,我们研究了色胺酮对白血病K562细胞的增殖衰减和凋亡诱导作用,并探讨了其潜在机制。结果表明,MTT分析和流式细胞仪分析证明,色胺酮可以以时间和剂量依赖性方式显着抑制K562细胞的增殖。在电子显微镜下,在存在色胺素的情况下,我们还观察到了角k病,染色质边缘化和凋亡小体的形成。还通过Hoechst 33258染色检测到核碎裂和凝结。暴露于色胺酮后,凋亡细胞的数量显着增加,而线粒体膜电位则显着降低。胰蛋白酶治疗组中的K562细胞表现出胞浆cyt-c,Bax和活化的caspase-3表达增加,而Bcl-2,mito cyt-c和pro-caspase-3含量降低。但是,全胱天蛋白酶抑制剂ZVAD-FMK可以消除前胱天蛋白酶3和活化的胱天蛋白酶3的变化。这些结果表明色胺酮对K562细胞具有增殖减弱和凋亡诱导作用。潜在的机制可能归因于线粒体膜电位的降低,线粒体cyt-c的释放和前胱天蛋白酶-3的激活。

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