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异甘草素体外诱导PC-12细胞毒性。

Isoliquiritigenin Induces Cytotoxicity in PC-12 Cells In Vitro.

作者信息

Yang Hui-Hui, Zhang Cheng, Lai Shang-Hai, Zeng Chuan-Chuan, Liu Yun-Jun, Wang Xiu-Zhen

机构信息

School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, People's Republic of China.

Guangdong Cosmetics Engineering and Technology Research Center, Guangzhou, 510006, People's Republic of China.

出版信息

Appl Biochem Biotechnol. 2017 Dec;183(4):1173-1190. doi: 10.1007/s12010-017-2491-7. Epub 2017 May 9.

Abstract

Isoliquiritigenin (ISL) has been reported to have a wide range of biological activities. This study evaluated the cytotoxic effect of ISL on norvegicus pheochromocytoma cell line (PC-12 cells) and its possible molecular mechanism. The cytotoxicity in vitro of ISL against PC-12 cells was investigated by MTT assay. The migration and invasion of PC-12 cells were performed by scratch test and transwell assay. Apoptosis was evaluated by microscopy and flow cytometry. The reactive oxygen species (ROS) and mitochondrial membrane potential were studied by fluorescent microscopy. DNA damage of PC-12 cells was analyzed by comet assay. The protein expression of caspase, Bcl-2 family member, autophagy-associated protein Beclin-1, and LC3 was detected by western blot. The autophagy of PC-12 cells was investigated by acridine orange (AO) and monodansylcadaverine (MDC) staining. The IC value of ISL against PC-12 cell is 17.8 ± 1.8 μM. ISL could suppress PC-12 cell migration and invasion. AO/ethidium bromide staining and flow cytometry suggested that ISL caused apoptosis of PC-12 cells. Significant DNA damages of PC-12 cells treated with ISL were observed in a comet assay. ISL inhibited the cell growth of PC-12 cells at S phase. Exposure of PC-12 cells to ISL increased the levels of cellular reactive oxygen species (ROS) and decreased the mitochondrial membrane potential. Additionally, ISL trigged the release of cytochrome c from the mitochondria to the cytoplasm. The expression levels of caspase-9, caspase-3, caspase-7, Bax, and Bim were upregulated, whereas the expression levels of Bcl-2 and Bcl-x were downregulated. AO and monodansylcadaverine (MDC) staining assay showed that ISL caused autophagy of PC-12 cells. The upregulation of protein Beclin-1 and LC3 was observed in PC-12 cells. Therefore, the results show that ISL induces apoptosis of PC-12 cells through ROS-mediated activation of the intrinsic mitochondria-cytochrome c-caspase protease mechanism and causes the autophagy of PC-12 cells. Graphical Abstract The in vitro cytotoxicity, apoptosis, comet assay, ROS, mitochondrial membrane potential, cell cycle arrest, autophagy, and western blot induced by ISL were investigated.

摘要

异甘草素(ISL)已被报道具有广泛的生物活性。本研究评估了ISL对挪威大鼠嗜铬细胞瘤细胞系(PC-12细胞)的细胞毒性作用及其可能的分子机制。采用MTT法研究ISL对PC-12细胞的体外细胞毒性。通过划痕试验和Transwell试验检测PC-12细胞的迁移和侵袭能力。通过显微镜检查和流式细胞术评估细胞凋亡情况。利用荧光显微镜研究活性氧(ROS)和线粒体膜电位。通过彗星试验分析PC-12细胞的DNA损伤。采用蛋白质印迹法检测半胱天冬酶、Bcl-2家族成员、自噬相关蛋白Beclin-1和LC3的蛋白表达。通过吖啶橙(AO)和单丹磺酰尸胺(MDC)染色研究PC-12细胞的自噬情况。ISL对PC-12细胞的IC值为17.8±1.8μM。ISL可抑制PC-12细胞的迁移和侵袭。AO/溴化乙锭染色和流式细胞术表明ISL可导致PC-12细胞凋亡。在彗星试验中观察到ISL处理的PC-12细胞存在明显的DNA损伤。ISL在S期抑制PC-12细胞的生长。PC-12细胞暴露于ISL会增加细胞内活性氧(ROS)水平并降低线粒体膜电位。此外,ISL引发细胞色素c从线粒体释放到细胞质中。半胱天冬酶-9、半胱天冬酶-3、半胱天冬酶-7、Bax和Bim的表达水平上调,而Bcl-2和Bcl-x的表达水平下调。AO和单丹磺酰尸胺(MDC)染色试验表明ISL可导致PC-12细胞自噬。在PC-12细胞中观察到Beclin-1和LC3蛋白的上调。因此,结果表明ISL通过ROS介导的内源性线粒体-细胞色素c-半胱天冬酶蛋白酶机制诱导PC-12细胞凋亡,并导致PC-12细胞自噬。图形摘要 研究了ISL诱导的体外细胞毒性、凋亡、彗星试验、ROS、线粒体膜电位、细胞周期阻滞、自噬和蛋白质印迹。

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