刘林华, 陈玉婷, 唐焕文, 张贺, 程小广, 杨慧, 凌晓璇. 氢醌对TK6细胞周期的影响及其相关的调控机制探讨[J]. 环境与职业医学, 2014, 31(2): 134-137. DOI: 10.13213/j.cnki.jeom.2014.0035
引用本文: 刘林华, 陈玉婷, 唐焕文, 张贺, 程小广, 杨慧, 凌晓璇. 氢醌对TK6细胞周期的影响及其相关的调控机制探讨[J]. 环境与职业医学, 2014, 31(2): 134-137. DOI: 10.13213/j.cnki.jeom.2014.0035
LIU Lin-hua , CHEN Yu-ting , TANG Huan-wen , ZHANG He , CHENG Xiao-guang , YANG Hui , LING Xiao-xuan . Effects of Hydroquinone on TK6 Cell Cycle and Related Regulatory Mechanism[J]. Journal of Environmental and Occupational Medicine, 2014, 31(2): 134-137. DOI: 10.13213/j.cnki.jeom.2014.0035
Citation: LIU Lin-hua , CHEN Yu-ting , TANG Huan-wen , ZHANG He , CHENG Xiao-guang , YANG Hui , LING Xiao-xuan . Effects of Hydroquinone on TK6 Cell Cycle and Related Regulatory Mechanism[J]. Journal of Environmental and Occupational Medicine, 2014, 31(2): 134-137. DOI: 10.13213/j.cnki.jeom.2014.0035

氢醌对TK6细胞周期的影响及其相关的调控机制探讨

Effects of Hydroquinone on TK6 Cell Cycle and Related Regulatory Mechanism

  • 摘要: 目的 探讨氢醌(hydroquinone,HQ)对细胞周期的影响及其相关的调控机制。

    方法 磷酸盐缓冲液(PBS)处理人类淋巴母细胞(TK6细胞)为对照组,20.0 μmol/L HQ为处理组,48 h后通过碘化丙啶(PI)标记的流式细胞术检测细胞周期分布情况,用实时荧光定量聚合酶链反应(qRT-PCR)检测PTEN (抑癌基因)、p53基因mRNA表达的改变,流式细胞荧光标记法检测Rb蛋白的表达。

    结果 与对照组比较,处理组G1期细胞比例明显增加,S期细胞比例明显减少,差异均有统计学意义(P<0.05);HQ作用于TK6细胞后上调了Rb的表达,下调了p53的表达,其差异均有统计学意义(P<0.05),而对PTEN的表达没有明显影响。

    结论 HQ可能通过上调Rb的表达使细胞阻滞于G1期。

     

    Abstract: Objective To investigate the effects of hydroquinone (HQ) on cell cycle and related regulatory mechanismin TK6 human lymphoblasts cells.

    Methods Phosphate buffered solution (PBS)-treated TK6 cells were selected as the controlgroup,and 20 μmol/L HQ-treated same line cells as the HQ-treated group.The distribution of cell cycle was determined with a flowcytometry kit using propidium iodide (PI) staining,the mRNA expressions of PTEN and p53 were quantified by reverse transcriptionreal-time polymerase chain reaction assay,and Rb protein expression was measured by flow cytometry.

    Results Compared with thecontrol group,the proportion of G1-phase cells in the HQ-treated group was increased,while the proportion of S-phase cells was decreased,and significant differences in the above indicators were observed between the two groups (P<0.05).Up-regulated expression of Rb proteinand down-regulated expression of p53 mRNA were observed in the HQ-treated group (P<0.05),but no significant effect on the expressionof PTEN mRNA was observed.

    Conclusion HQ may arrest TK6 cells at G1 phase by raising the expression of Rb protein.

     

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