【打印本页】 【下载PDF全文】 【HTML】 查看/发表评论下载PDF阅读器关闭

←前一篇|后一篇→

过刊浏览    高级检索

本文已被:浏览 2928次   下载 2188 本文二维码信息
码上扫一扫!
芦荟大黄素介导的光动力诱导骨肉瘤MG63细胞自噬
涂平华1,李开庭2,陈青2,欧云生1*,白定群2*
0
(1. 重庆医科大学附属第一医院骨科, 重庆 400016;
2. 重庆医科大学附属第一医院康复科, 重庆 400016
*通信作者)
摘要:
目的 探讨芦荟大黄素(aloe emodin,AE)介导的光动力(aloe emodin-photodynamic therapy,AE-PDT)诱导骨肉瘤MG63细胞产生自噬, 并探讨自噬和凋亡的关系。方法 将细胞分为AE-PDT对照组(Control组、AE组、LED组)和AE-PDT实验组。AE-PDT作用于人骨肉瘤MG63细胞后, 采用CCK-8法检测细胞活性, 2',7'-二氯荧光二乙酸盐(2',7'-dichlorofluorescin diacetate, DCFH-DA)荧光检测细胞活性氧(reactive oxygen species,ROS)水平, 单丹磺酰尸胺(monodansylcadaverin, MDC)染色检测细胞的自噬小体, 透射电镜观察细胞的自噬体, 流式细胞仪检测细胞凋亡情况, Western 印迹检测自噬相关蛋白微管相关蛋白1轻链3(LC3)和Beclin-1的表达。结果 AE-PDT能明显抑制人骨肉瘤MG63细胞的活性, 且其抑制作用呈芦荟大黄素浓度-光动力能量剂量依赖性。AE-PDT实验组细胞内ROS水平和自噬小体均较3个对照组增高;透射电镜下可见典型自噬体;AE-PDT能诱导细胞产生自噬和凋亡, 3-甲基腺嘌呤抑制自噬后能增加细胞的凋亡率(P<0.05);Western印迹检测LC3-Ⅱ/LC3-Ⅰ和Beclin-1/β-actin的表达高于阴性对照组。结论 AE-PDT能诱导骨肉瘤MG63细胞产生自噬。AE-PDT作用早期, 自噬能延缓凋亡的发生可能起保护性作用。
关键词:  芦荟大黄素  光动力疗法  骨肉瘤  自噬
DOI:10.3724/SP.J.1008.2014.01347
投稿时间:2014-06-04修订日期:2014-09-25
基金项目:国家自然科学基金(81101692), 重庆市科委自然科学基金(2011BB5136).
Autophagy of osteosarcoma MG63 cells induced by aloe emodin-mediated photodynamic therapy
TU Ping-hua1,LI Kai-ting2,CHEN Qing2,OU Yun-sheng1*,BAI Ding-qun2*
(1. Department of Orthopedics, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China;
2. Department of Rehabilitation Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
*Corresponding authors)
Abstract:
Objective To investigate the autophagy of osteosarcoma MG63 cells induced by aloe emodin-mediated photodynamic therapy, and to discuss the relationship between autophagy and apoptosis. Methods The cultured MG63 cells were divided into 4 groups: empty control group, AE group, LED group, and AE-PDT group. MG63 cells in AE-PDT group were treated with aloe emodin combined with photodynamic therapy. The cell viability was measured by CCK-8, the DCFH-DA probe was used to detect cell ROS level, the autophagosomes were examined by MDC staining and electron microscope, the apoptosis of MG63 cells was detected by flow cytometry, and the autophagy-related protein (LC3 and Beclin-1) expressions were assessed by Western blotting analysis. Results Photosensitizer aloe emodin-mediated PDT significantly suppressed cell viability in a photosensitizer concentration- and energy density-dependent manner. The ROS level and autophagosomes were significantly increased in the AE-PDT group, with classical autophagosomes found under the electron microscope. AE-PDT induced autophagy and apoptosis of MG63 cells. The apoptosis rate was significantly increased when autophagy was inhibited by 3-MA (P<0.05).The results of Western blotting analysis showed that ratios of LC3-Ⅱ/LC3-Ⅰ and Beclin-1/β-actin in AE-PDT group were higher than those in the single AE treatment group, single light irradiation group, and the empty control group. Conclusion AE-PDT can induce autophagy in the MG63 cells. At the early stage of AE-PDT treatment, autophagy can postpone apoptosis and hence exert a protective effect.
Key words:  aloe emodin  photodynamic therapy  osteosarcoma  autophagy