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朱佳玉, 陈锋, 吕航, 王惠惠, 皮静波. 镉暴露对HepG2细胞NRF2信号通路影响[J]. 中国公共卫生, 2017, 33(4): 584-588. DOI: 10.11847/zgggws2017-33-04-17
引用本文: 朱佳玉, 陈锋, 吕航, 王惠惠, 皮静波. 镉暴露对HepG2细胞NRF2信号通路影响[J]. 中国公共卫生, 2017, 33(4): 584-588. DOI: 10.11847/zgggws2017-33-04-17
ZHU Jia-yu, CHEN Feng, LÜ Hang.et al, . Effects of cadmium exposure on NRF2 signaling pathway in HepG2 cells[J]. Chinese Journal of Public Health, 2017, 33(4): 584-588. DOI: 10.11847/zgggws2017-33-04-17
Citation: ZHU Jia-yu, CHEN Feng, LÜ Hang.et al, . Effects of cadmium exposure on NRF2 signaling pathway in HepG2 cells[J]. Chinese Journal of Public Health, 2017, 33(4): 584-588. DOI: 10.11847/zgggws2017-33-04-17

镉暴露对HepG2细胞NRF2信号通路影响

Effects of cadmium exposure on NRF2 signaling pathway in HepG2 cells

  • 摘要: 目的 探讨镉暴露对HepG2细胞转录因子NF-E2相关因子2(NRF2)信号通路的影响。方法 采用甲臢比色法测定CdCl2(0、1、2.5、5、10、25、50、100、200 μmol/L)处理24 h后,HepG2细胞活力变化;应用蛋白免疫印迹法检测CdCl2(1、2、5、10、20 μmol/L)处理细胞6 h后,NRF2蛋白水平;采用RT-qPCR方法检测10 μmol/L CdCl2处理细胞2、4、6、12、24 h后,GCLC、GCLM、HO1 和 AKR1C1 mRNA水平变化,检测CdCl2(1、2、5、10、20 μmol/L)处理细胞6 h后,GCLC、GCLM、HO1和AKR1C1 mRNA水平变化。结果 HepG2细胞活力随镉处理剂量升高而降低(P<0.05);与对照组(0.60±0.01)比较, 1、2、5、10、20 μmol/L镉处理组HepG2细胞NRF2蛋白表达水平分别为(0.65±0.01)、(1.37±0.04)、(1.94±0.05)、(2.24±0.07)、(2.22±0.05)均明显升高(P<0.05);与对照组比较,镉处理6 h时,HepG2细胞内GCLC、GCLM、HO1和AKR1C1 mRNA水平分别为(45.76±7.04)、(114.21±5.23)、(59.52±1.50)、(674.13±27.12)明显升高(P<0.05);与对照组比较,5 μmol/L镉处理组HepG2细胞内GCLC和GCLM mRNA水平分别为(24.77±2.16)、(29.93±0.67)升高,2 μmol/L镉处理组HepG2细胞内HO1和AKR1C1 mRNA水平分别(28.55±2.02)、(186.32±12.63)升高(P<0.05)。结论 镉暴露能激活HepG2细胞系中NRF2信号通路。

     

    Abstract: Objective To explore the effects of cadmium exposure on nuclear factor erythroid 2-related factor 2 (NRF2) signaling pathway in HepG2 cells.Methods The HepG2 cells were treated with cadmium chloride (CdCl2) at dosages of 0,1,2.5,5,10,25,50,100,and 200 μmol/L for 24 hours and then the viability of the cells was measured with 3-(4,5-dimethylthiazol-2-yl)-5(3-carboxymethonyphenol)-2-(4-sulfophenyl)-2H-tetrazolium (MTS);the cells were treated with CdCl2 (1,2,5,10,and 20 μmol/L) for 6 hours and the protein levels of NRF2 were determined with Western blot;the cells were treated with 10 μmol/L CdCl2 for 2,4,6,12,and 24 hours and the mRNA levels of Nrf2 downstream genes glutamate-cysteine ligase catalitic subunit (GCLC),glutamate cysteine ligase modifier (GCLM),heme oxygenase 1 (HO1),and aldo-keto reductase family 1 member (AKR1C1) were determined with reverse transcriptase quantitative polymerase chain reaction (RT-qPCR);the cells were treated with 1,2,5,10,and 20 μmol/L CdCl2 for 6 hours and the mRNA levels of Nrf2 downstream genes GCLC,GCLM,HO1,and AKR1C1 were determined by RT-qPCR.Results The cell viability significantly decreased with the increased concentration of CdCl2 in HepG2 cells (P<0.05).Compared to that (0.60±0.01) of the control group,the expression levels of NRF2 protein significantly increased (0.65±0.01,1.37±0.04,1.94±0.05,2.24±0.07,and 2.22±0.05 in the cells with 1,2,5,10 and 20 μmol/L cadmium exposure (P<0.05 for all).Compared with those of the control group,the mRNA levels of NRF2 downstream genes of GCLC,GCLM,HO1,and AKR1C1 significantly increased (45.76±7.04,114.21±5.23,59.52±1.50,and 674.13±27.12) in the cells with 6 hours' cadmium exposure (P<0.05 for all).Compared with those of the control group,the mRNA levels of NRF2 downstream genes of GCLC and GCLM significantly increased (24.77±2.16 and 29.93±0.67) in the cells treated with 5 μmol/L cadmium,and those of HO1 and AKR1C1 also increased significantly (28.55±2.02 and 186.32±12.63) in the cells treated with 2 μmol/L cadmium (all P<0.05).Conclusion Cadmium exposure can activate NRF2 signaling pathway in HepG2 cell line.

     

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