›› 2010, Vol. 41 ›› Issue (2): 228-231.doi: 10.3969/j.issn.0529-1356.2010.02.012

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三氮唑席夫碱衍生物诱导SMMC-7721细胞自相残

孙玉生; 皇甫超申*;刘彬 ;马永超 ;胡国强   

  1. 河南大学神经生物学研究所 河南大学医学院,河南 开封 475004
  • 收稿日期:2009-04-29 修回日期:2009-06-08 出版日期:2010-04-06
  • 通讯作者: 皇甫超申

Triazole Schiff base derivative induces cannibalism of SMMC-7721 cells EM>in vitro/EM>

  1. Institute of Neurobiology,Medical College of He′nan University, He′nan Kaifeng 475004, China
  • Received:2009-04-29 Revised:2009-06-08 Online:2010-04-06
  • Contact: HUANGFU Chao-shen

关键词: 三氮唑席夫碱衍生物, 肝癌细胞, 自相残, 免疫组织化学, 透射电镜, 人

Abstract: Objective To a nalyze the morphologic features of SMMC-7721 cannibalistic cells that induced by triazole Schiff base derivative(LH-37) EM>in vitro/EM>. Methods The SMMC-7721 cells (1×10SUP>4/SUP>/ml)were cultured in the medium containing of 1×10SUP>-5/SUP> mol/L LH-37 for 24h,48hThe character of cells was detected by Papanicolaou and Wright′s Staining. Immunohistochemical method was used to observe the cleaved Caspase-3 positive cells. The ultrastructure of cannibalism cells was observed by JEM 100CXII transmission electronic microscope. Results Microscopic analysis demonstrated the complete internalization of one cell within another. We noted that some cannibalistic cells in small aggregates appeared to be inside of large vacuoles, suggesting that they were internalized within a neighboring cell. The proportion of cannibalistic cells were increased after SMMC-7721 cells were cultured in the presence of LH-37 for 48 hours. The proportion of the cannibalistic cells in control and LH-37 group was 0.47% and 5.23% respectively. Many internalized cells were positive for cleaved Caspase-3 staining . Ultrastructural analysis of engulfed cells from 24 hours exhibited evidence of livecell internalization consistent with cannibalism, The most common fate for internalized cells was death after treatment with LH-37 for 48 hours, as evidenced by nuclear degradation and the

Key words: Triazole Schiff base derivative, Hepatocarcinoma cell, Cannibalism, Immunohistochemistry, Transmission electronic microscopy, Human

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