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山茱萸粗提取物通过活性氧调节的途径诱导U-2 OS人骨肉瘤细胞发生凋亡性细胞死亡。

The crude extract of Corni Fructus induces apoptotic cell death through reactive oxygen species-modulated pathways in U-2 OS human osteosarcoma cells.

作者信息

Liao Ching-Lung, Hsu Shu-Chun, Yu Chien-Chih, Yang Jai-Sing, Tang Nou-Ying, Wood Wellington Gibson, Lin Jaung-Geng, Chung Jing-Gung

机构信息

Graduate Institute of Chinese Medicine, China Medical University, Taichung 404, Taiwan, Republic of China.

出版信息

Environ Toxicol. 2014 Sep;29(9):1020-31. doi: 10.1002/tox.21832. Epub 2012 Dec 12.

DOI:10.1002/tox.21832
PMID:23239598
Abstract

Crude extract of Corni Fructus (CECF) has been used in Traditional Chinese medicine for the treatment of different diseases for hundreds of years. The purpose of this study was to investigate the cytotoxic effects of CECF on U-2 OS human osteosarcoma cells. Flow cytometry was used for measuring the percentage of viable cells, cell-cycle distribution, apoptotic cells in sub-G1 phase, reactive oxygen species (ROS), Ca(2+) levels, and mitochondrial membrane potential (ΔΨm ). Comet assay and 4'-6-diamidino-2-phenylindole staining were used for examining DNA damage and condensation. Western blotting was used to examine apoptosis-associated protein levels in U-2 OS cells after exposed to CECF. Immunostaining and confocal laser system microscope were used to examine protein translocation after CECF incubation. CECF decreased the percentage of viability, induced DNA damage and DNA condensation, G₀/G₁ arrest, and apoptosis in U-2 OS cells. CECF-stimulated activities of caspase-8, caspase-9, and caspase-3, ROS, and Ca(2+) production, decreased ΔΨm levels of in U-2 OS cells. CECF increased protein levels of caspase-3, caspase-9, Bax, cytochrome c, GRP78, AIF, ATF-6α, Fas, TRAIL, p21, p27, and p16 which were associated with cell-cycle arrest and apoptosis. These findings suggest that CECF triggers apoptosis in U-2 OS cells via ROS-modulated caspase-dependent and -independent pathways.

摘要

山茱萸粗提物(CECF)在传统中药中用于治疗多种疾病已有数百年历史。本研究旨在探讨CECF对U-2 OS人骨肉瘤细胞的细胞毒性作用。采用流式细胞术检测活细胞百分比、细胞周期分布、亚G1期凋亡细胞、活性氧(ROS)、Ca²⁺水平和线粒体膜电位(ΔΨm)。彗星试验和4',6-二脒基-2-苯基吲哚染色用于检测DNA损伤和凝聚。蛋白质印迹法用于检测U-2 OS细胞暴露于CECF后凋亡相关蛋白水平。免疫染色和共聚焦激光系统显微镜用于检测CECF孵育后蛋白质转位。CECF降低了U-2 OS细胞的活力百分比,诱导了DNA损伤和DNA凝聚、G₀/G₁期阻滞及凋亡。CECF刺激了U-2 OS细胞中半胱天冬酶-8、半胱天冬酶-9和半胱天冬酶-3的活性、ROS及Ca²⁺生成,降低了ΔΨm水平。CECF增加了与细胞周期阻滞和凋亡相关的半胱天冬酶-3、半胱天冬酶-9、Bax、细胞色素c、GRP78、AIF、ATF-6α、Fas、TRAIL、p21、p27和p16的蛋白水平。这些发现表明,CECF通过ROS调节的半胱天冬酶依赖性和非依赖性途径触发U-2 OS细胞凋亡。

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