畜牧兽医学报 ›› 2005, Vol. 36 ›› Issue (4): 328-332.

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2种锌源对体外培养胸腺细胞Bcl-2、Bax、Caspase-3 mRNA表达的影响

虞泽鹏; 乐国伟; 施用晖   

  1. 1.教育部食品科学与安全重点实验室,无锡 214036; 2.江南大学食品营养与安全研究所,无锡 214036
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2005-04-25 发布日期:2005-04-25

Effects of Zinc Sulfate and Zinc Methionine on Bcl-2, Bax, Caspase-3 mRNAExpression of Thymocytes in vitro

YU Ze-peng; LE Guo-wei;SHI Yong-hui   

  1. 1.Key Laboratory of Food Science and Safety,Ministry of Education,Wuxi 214036,China;2.Food Nutrition and Safety Institute,School of Food Science and Technology, Southern Yangtze University, Wuxi 214036, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2005-04-25 Published:2005-04-25

摘要: 采用地噻咪松作为诱导剂,建立小鼠胸腺细胞体外培养的凋亡模型,培养基中分别补加1 000 μmol/L的硫酸锌或蛋氨酸锌,培养16 h。测定细胞的凋亡率、DNA片段化以及Bcl-2、Bax、Caspase-3 mRNA 表达量。结果表明,地噻咪松显著提高体外培养腺细胞凋亡(P<0.01),并上调Bcl-2、Bax、Caspase-3 3种基因的mRNA表达(P<0.01)。硫酸锌和蛋氨酸锌对地噻咪松诱导的凋亡均有显著的抑制作用(P<0.01),并对上述3种基因表达的上调有抑制作用(P<0.01)。蛋氨酸锌处理的细胞凋亡率及Caspase-3 mRNA表达均高于硫酸锌处理,Caspase-3 mRNA表达量差异达到了显著水平(P<0.05)。这表明,锌调控糖皮质激素诱导的细胞凋亡涉及到对基因转录水平的调节,2种锌源在一定程度上存在着差异。

关键词: 硫酸锌, 蛋氨酸锌, 体外培养, 胸腺细胞, 凋亡, 基因表达

Abstract: To investigate the effects of different zinc sources on Bcl-2, Bax, Caspase-3 mRNA expression, dexamethasone was used to make the apoptosis model of thymocytes. Zinc sulfate and zinc methionine was added to the medium at the level of 1 000 μmol/L, the percentage of apoptosis nuclei were determined by flow cytometric analysis, Bcl-2, Bax, Caspase-3 mRNA were measured by RT-PCR. The results showed that both ZnSO4 and Zn-Met can modulate apoptosis induced by dexamethasone, they inhibited apoptosis (P<0.01) and decreased DNA ladder happening; no difference was shown of modulating apoptosis between the two kinds of zinc (P>0.05). Both kinds of zinc could inhibit the upregulating of Bcl-2, Bax, Caspase-3 mRNA induced by dexamethasone (P<0.01). Cell availability and Caspase-3 mRNA expression of cells cultured with Zn-Met were higher than those cultured with ZnSO4 (P<0.05). The percentage of apoptosis nuclei, Bcl-2, Bax mRNA expression were similar within two groups (P>0.05). We draw the conclusion that both kinds of zinc could modulate apoptosis of thymocytes induced by glucocorticoid; the mechanism may involve the regulating ability of zinc on genes expression, and the two forms of zinc may go different ways in the regulations.

Key words: zinc sulfate, zinc-methionine, in vitro, thymocyte, apoptosis, gene expression