氧化苦参碱通过COX-2/PINK1/Parkin信号通路介导的线粒体自噬对MG63骨肉瘤细胞的促凋亡机制 点击下载
| 论文标题： | 氧化苦参碱通过COX-2/PINK1/Parkin信号通路介导的线粒体自噬对MG63骨肉瘤细胞的促凋亡机制 |
| 英文标题： | |
| 中文摘要： | 目的 基于环氧合酶2（COX-2）/PTEN诱导激酶1（PINK1）/帕金森病蛋白2（Parkin）信号通路介导的线粒体自噬研究氧化苦参碱对人骨肉瘤MG63细胞的促凋亡机制。方法取MG63细胞经2.0、4.0、8.0mg/mL的氧化苦参碱和6μmol/L的5-氟尿嘧啶（5-FU）作用后，检测细胞凋亡率、凋亡相关蛋白[B细胞淋巴瘤2（Bcl-2）、Bcl-2相关X蛋白（Bax）]表达水平、线粒体膜电位降低比例、线粒体自噬水平以及PINK1、Parkin、微管相关蛋白1轻链3Ⅱ（LC3-Ⅱ）蛋白表达水平。采用PINK1小干扰RNA（PINK1siRNA）干扰PINK1的表达，将细胞分为对照组、PINK1siRNA组、氧化苦参碱组、PINK1siRNA+氧化苦参碱组，检测细胞中PINK1、Parkin、LC3-Ⅱ蛋白表达水平和线粒体膜电位降低比例以及细胞凋亡率。采用慢病毒感染使COX-2过表达，将细胞分为对照组、氧化苦参碱组、COX-2组、COX-2+氧化苦参碱组，检测细胞中COX-2、PINK1和Parkin蛋白表达水平以及线粒体膜电位降低比例。结果经氧化苦参碱干预后，细胞凋亡率，Bax、PINK1、Parkin、LC3-Ⅱ蛋白表达水平，线粒体自噬水平和线粒体膜电位降低比例均显著升高（P＜0.05），Bcl-2蛋白表达水平显著降低（P＜0.05）。与氧化苦参碱组比较，PINK1siRNA+氧化苦参碱组细胞中PINK1、Parkin、LC3-Ⅱ蛋白表达水平和细胞凋亡率以及线粒体膜电位降低比例均显著降低（P＜0.05）。与氧化苦参碱组比较，COX-2+氧化苦参碱组细胞中COX-2蛋白表达水平显著升高（P＜0.05），PINK1、Parkin蛋白表达水平和线粒体膜电位降低比例均显著降低（P＜0.05）。结论氧化苦参碱可通过抑制COX-2表达，介导线粒体自噬信号通路PINK1/Parkin的过度活化，从而促进骨肉瘤细胞凋亡。 |
| 英文摘要： | OBJECTIVE To study the mechanism of oxymatrine inducing apoptosis of osteosarcoma MG63 cell line based on mitophagy mediated by cyclooxygenase-2 （COX-2）/PTEN-induced putative kinase-1 （PINK1）/Parkinson disease protein-2 （Parkin） signaling pathway. METHODS MG63 cells were treated with 2.0， 4.0， 8.0 mg/mL oxymatrine and 6 μmol/L 5-fluorouracil， then the apoptotic rate， the expression of apoptosis-related proteins [B-cell lymphoma-2 （Bcl-2）， Bcl-2 related X protein （Bax）]， the proportion of decrease in mitochondrial membrane potential， the level of mitophagy as well as the protein expressions of PINK1， Parkin， and microtubule-associated protein 1 light chain-3Ⅱ （LC3-Ⅱ） were detected. PINK1 small interfering RNA （siRNA） was adopted to intervene in the expression of PINK1， the cells were divided into control group， PINK1 siRNA group， oxymatrine group， and PINK1 siRNA+oxymatrine group； the protein expressions of PINK1， Parkin， and LC3-Ⅱ， the proportion of decrease in mitochondrial membrane potential （MMP） as well as apoptotic rate were detected. The lentivirus infection technique was used to overexpress COX-2， the cells were divided into control group， oxymatrine group， COX-2 group， and COX-2+oxymatrine group. The protein expressions of COX-2， PINK1， and Parkin， as well as the proportion of decrease in MMP were detected. RESULTS After being treated with oxymatrine， the apoptotic rate， the protein expressions of Bax， PINK1， Parkin， and LC3-Ⅱ， the level of mitophagy as well as the proportion of decrease in MMP were significantly increased （P＜0.05）， while the protein expression of Bcl-2 was significantly decreased （P＜0.05）. Compared with the oxymatrine group， the protein expressions of PINK1， Parkin， and LC3-Ⅱ， apoptotic rate and the proportion of decrease in MMP were significantly decreased in PINK1 siRNA+oxymatrine group （P＜0.05）. Compared with the oxymatrine group， the protein expression of COX-2 in the COX-2+oxymatrine group was increased significantly （P＜0.05）， while the protein expressions of PINK1 and Parkin as well as the proportion of 526087266@qq.com decrease in MMP were decreased significantly （P＜0.05）. CONCLUSIONS Oxymatrine can mediate the overactivity of mitophagy based on the PINK1/Parkin signaling pathway by inhibiting COX-2 expression， thus promoting the apoptosis of the MG63 osteosarcoma cell line. |
| 期刊： | 2024年第35卷第01期 |
| 作者： | 姬健钧；邱文奎 |
| 英文作者： | JI Jianjun，QIU Wenkui |
| 关键字： | 氧化苦参碱；骨肉瘤；细胞凋亡；线粒体自噬；环氧合酶2；PTEN诱导激酶1；帕金森病蛋白2 |
| KEYWORDS： | oxymatrine； osteosarcoma； cell apoptosis； mitophagy； cyclooxygenase-2； PTEN-induced putative kinase protein- |
| 总下载数： | 81次 |
| 本日下载数： | 2次 |
| 本月下载数： | 81次 |
| 文件大小： | 619.60Kb |
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