...
首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Proteomic analysis identifies differentially expressed proteins after red propolis treatment in Hep-2 cells
【24h】

Proteomic analysis identifies differentially expressed proteins after red propolis treatment in Hep-2 cells

机译:蛋白质组学分析鉴定了在Hep-2细胞中红色蜂胶处理后差异表达的蛋白质

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Here we investigated alterations in the protein profile of Hep-2 treated with red propolis using two-dimensional electrophoresis associated to mass spectrometry and apoptotic rates of cells treated with and without red propolis extracts through TUNEL and Annexin-V assays. A total of 325 spots were manually excised from the two-dimensional gel electrophoresis and 177 proteins were identified using LC-MS-MS. Among all proteins identified that presented differential expression, most were down-regulated in presence of red propolis extract at a concentration of 120. μg/mL (IC50): GRP78, PRDX2, LDHB, VIM and TUBA1A. Only two up-regulated proteins were identified in this study in the non-cytotoxic (6. μg/mL) red propolis treated group: RPLP0 and RAD23B. TUNEL staining assay showed a markedly increase in the mid- to late-stage apoptosis of Hep-2 cells induced by red propolis at concentrations of 60 and 120. μg/mL when compared with non-treated cells. The increase of late apoptosis was confirmed by in situ Annexin-V analysis in which red propolis extract induced late apoptosis in a dose-dependent manner. The differences in tumor cell protein profiles warrant further investigations including isolation of major bioactive compounds of red propolis in different cell lines using proteomics and molecular tests to validate the protein expression here observed.
机译:在这里,我们通过二维电泳,通过TUNEL和膜联蛋白-V测定法,对与质谱法相关的二维电泳和细胞凋亡率进行了研究,研究了用红色蜂胶处理过的Hep-2的蛋白质谱中的变化以及细胞凋亡率。从二维凝胶电泳中手动切除了总共325个斑点,并使用LC-MS-MS鉴定了177种蛋白质。在鉴定出呈现差异表达的所有蛋白质中,大多数在浓度为120.μg/ mL(IC50)的红色蜂胶提取物中被下调:GRP78,PRDX2,LDHB,VIM和TUBA1A。在本研究中,在非细胞毒性(6.μg/ mL)红色蜂胶治疗组中仅发现了两种上调的蛋白:RPLP0和RAD23B。 TUNEL染色法显示,与未经处理的细胞相比,浓度为60和120.μg/ mL的红色蜂胶诱导的Hep-2细胞的中晚期凋亡明显增加。通过原位膜联蛋白-V分析证实了晚期细胞凋亡的增加,其中红色蜂胶提取物以剂量依赖性方式诱导了晚期细胞凋亡。肿瘤细胞蛋白质谱的差异值得进一步研究,包括使用蛋白质组学和分子测试分离不同细胞系中红色蜂胶的主要生物活性化合物,以验证此处观察到的蛋白质表达。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号