络石内生菌露湿漆斑菌发酵液的细胞毒活性成分研究

Study on cytotoxic active constituents in fermentation liquid of endophytic fungus Myrothecium roridum in Trachelospermum jasminoide

  • 摘要:
      目的  研究络石内生菌露湿漆斑菌(Myrothecium roridum)发酵液的细胞毒活性成分,以期获得结构新颖、活性显著的化合物,为发现抗肿瘤先导化合物提供实验依据。
      方法  以氢谱(1H-NMR谱)和薄层色谱(TLC)示踪,采用硅胶柱层析、Sephadex LH-20凝胶柱层析和高效液相色谱法(HPLC)进行发酵液浸膏的分离纯化; 利用高分辨质谱、核磁共振谱及文献比对方法鉴定化合物的结构; 采用MTT法测定化合物对HepG2细胞和Hela细胞的体外细胞毒活性,顺铂为阳性对照药; 采用流式细胞术分析化合物对肿瘤细胞的细胞周期影响; 采用Western blot法检测化合物处理后肿瘤细胞中细胞周期负调控蛋白p27的表达水平。
      结果  从M. roridum发酵液中分离获得2个单端孢霉烯化合物12′-hydroxyroridin E (1)和trichoverritone (2), 其对HepG2细胞和Hela细胞有明显的增殖抑制作用, IC50值分别为0.78和1.86 μg/mL、0.05和0.13 μg/mL, 阳性对照药顺铂的IC50值分别为4.9和2.28 μg/mL。进一步研究发现, 12′-hydroxyroridin E (1)能诱导HepG2细胞G2期周期阻滞,且上调细胞中p27蛋白的表达。
      结论  12′-hydroxyroridin E (1)可能通过诱导HepG2细胞G2期周期阻滞而抑制其增殖抑制,该诱导作用可能与细胞中p27蛋白的表达上调相关。

     

    Abstract:
      Objective  To study the cytotoxic constituents in fermentation liquid of endophytic fungus Myrothecium roridum in Trachelospermum jasminoide so as to find compounds with novel structure and strong activity and to provide experimental basis for discovery of anticancer leading compounds.
      Methods  Guided by 1H-NMR magnetic resonance spectrum(1H-NMR)and thin-layer chromatography(TLC), isolation and purification of the extract of liquid culture were performed through silica gel column chromatography, Sephadex LH-20 gel filtration chromatography and high performance liquid chromatography(HPLC). Structures of compounds were identified by high resolution mass spectrum and nuclear magnetic resonance spectrum and comparison with data of literatures. In vitro cytotoxic activity of compounds to HepG2 cells and Hela cells were evaluated through MTT method and cisplatin was used as positive control. Flow cytometry was used to analyse the effect of compound on the cell cycle of tumor cells and Western blot to detect the expression level ofnegative regulatory protein p27 in a cell cycle.
      Results  Two trichothecene compounds, including 12′-hydroxyroridin E (1) and trichoverritone (2) were isolated from the fermentation broth of M. roridum, which had obvious inhibitory effect on HepG2 and Hela cells. The IC50 values of two compounds were 0.78 and 1.86 μg/mL, 0.05 and 0.13 μg/mL, respectively, and were 4.9 and 2.28 μg/mL, respectively, in cisplatin. Further study indicated that 12′-hydroxyroridin E (1) could induce G2 phase arrest in HepG2 cells and up-regulate the expression level of protein p27.
      Conclusion  12′-hydroxyroridin E (1) could block G2 phase cell cycle in HepG2 cells to inhibit cell proliferation, which is related to the up-regulated expression of protein p27.

     

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