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从龙葵中分离出的糖蛋白通过凋亡作用杀死 HT - 29 细胞。

Glycoprotein isolated from Solanum nigrum L. kills HT-29 cells through apoptosis.

作者信息

Lim Kye-Taek

机构信息

#521 Molecular Biochemistry Laboratory, Institute of Biotechnology, Chonnam National University, Yongbong Dong, Kwangju, Korea.

出版信息

J Med Food. 2005 Summer;8(2):215-26. doi: 10.1089/jmf.2005.8.215.

Abstract

Solanum nigrum L. (SNL) has been used in folk medicine for its anti-inflammatory activity. We previously isolated glycoprotein from SNL and observed that it decreased viable HT-29 cell numbers at a low concentration (60 microg/mL). This study investigated the apoptotic signal pathway triggered by glycoprotein isolated from SNL in HT-29 cells. Treatment of HT-29 cells with SNL glycoprotein (60 microg/mL) for 4 hours resulted in a cytotoxic effect of more than 60%, compared with the control. To explain the apoptotic effects of SNL glycoprotein, we investigated its effects on 12-O-tetradecanoylphorbol 13-acetate (TPA)-stimulated protein kinase C (PKC) alpha activity and DNA-binding activity of nuclear factor (NF) kappaB in HT-29 cells, using western blot analysis and electrophoretic mobility shift assays. Results from these experiments showed that SNL glycoprotein has remarkable inhibitory effects on the activities of TPA (100 nM)-stimulated PKCalpha and NF-kappaB in HT-29 cells. They also substantiated that PKCalpha is a part of the TPA-activated upstream signal pathway of NF-kappaB, since NF-kappaB activity was inhibited by staurosporine (a PKC inhibitor) and pyrrolidine dithiocarbamate (an NF-kappaB inhibitor) in a western blot analysis. Furthermore, to verify the triggering of apoptosis by the SNL glycoprotein, we performed DNA fragmentation, nuclear staining, and protein expression assays of apoptotic-related proteins. The amount of DNA fragmentation and apoptotic cell numbers increased in a dose-dependent manner after treatment with SNL glycoprotein. Apoptosis-related protein assays demonstrated that SNL glycoprotein-induced apoptosis is associated with the regulation of bcl-2 and Bax expression. Taken together, the results of this study showed that the activation of PKCalpha, NF-kappaB, and Bax expression by SNL glycoprotein is possibly involved in the apoptotic process. Consequently, these results indicate that SNL glycoprotein causes HT-29 cell death through apoptosis by its ability to modulate anti-apoptotic signals. We suggest that SNL glycoprotein is a natural anti-cancer agent due to its potential to induce apoptosis in HT-29 cells.

摘要

龙葵(Solanum nigrum L.,SNL)因其抗炎活性而被用于民间医学。我们之前从龙葵中分离出了糖蛋白,并观察到它在低浓度(60微克/毫升)时会降低HT - 29细胞的存活数量。本研究调查了从龙葵中分离出的糖蛋白在HT - 29细胞中触发的凋亡信号通路。用龙葵糖蛋白(60微克/毫升)处理HT - 29细胞4小时,与对照组相比,产生了超过60%的细胞毒性作用。为了解释龙葵糖蛋白的凋亡作用,我们使用蛋白质免疫印迹分析和电泳迁移率变动分析,研究了其对12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)刺激的蛋白激酶C(PKC)α活性以及HT - 29细胞核因子(NF)κB的DNA结合活性的影响。这些实验结果表明,龙葵糖蛋白对HT - 29细胞中TPA(100纳摩尔)刺激的PKCα和NF - κB活性具有显著的抑制作用。它们还证实PKCα是TPA激活的NF - κB上游信号通路的一部分,因为在蛋白质免疫印迹分析中,NF - κB活性受到星形孢菌素(一种PKC抑制剂)和吡咯烷二硫代氨基甲酸盐(一种NF - κB抑制剂)的抑制。此外,为了验证龙葵糖蛋白是否触发凋亡,我们进行了DNA片段化、细胞核染色以及凋亡相关蛋白的表达分析。用龙葵糖蛋白处理后,DNA片段化的量和凋亡细胞数量呈剂量依赖性增加。凋亡相关蛋白分析表明,龙葵糖蛋白诱导的凋亡与bcl - 2和Bax表达的调节有关。综上所述,本研究结果表明,龙葵糖蛋白对PKCα、NF - κB的激活以及Bax表达可能参与了凋亡过程。因此,这些结果表明,龙葵糖蛋白通过调节抗凋亡信号的能力,导致HT - 29细胞通过凋亡死亡。我们认为龙葵糖蛋白因其在HT - 29细胞中诱导凋亡的潜力而可能是一种天然抗癌剂。

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