癌变·畸变·突变
癌變·畸變·突變
암변·기변·돌변
CARCINOGENSES,TERATOGENSIS AND MUTAGENESIS
2015年
1期
64-67,70
,共5页
黄爱博%洪文旭%叶金波%刘建军%许华
黃愛博%洪文旭%葉金波%劉建軍%許華
황애박%홍문욱%협금파%류건군%허화
三氯乙烯%细胞毒性%SET相互作用蛋白%mRNA
三氯乙烯%細胞毒性%SET相互作用蛋白%mRNA
삼록을희%세포독성%SET상호작용단백%mRNA
trichloroethylene%cytotoxicity%SET-associated proteins%mRNA
目的:法:取对数生长期的L-02肝细胞,暴露于不同浓度TCE(1.0、2.0、4.0、8.0 mmol/L)中,以DMSO为溶剂对照。24 h后,采用实时荧光定量PCR检测eEF1A1、eEF1A2和DDB1 mRNA表达水平。结果:与对照组相比,不同浓度的TCE均能够使L-02肝细胞eEF1A1、eEF1A2和DDB1 mRNA表达水平发生明显变化。其中,DDB1和eEF1A2 mRNA表达水平在低浓度(1.0 mmol/L)TCE暴露下显著升高,而随着TCE浓度的升高其mRNA表达水平显著降低(P<0.05或<0.01)。eEF1A1 mRNA表达水平随着TCE浓度的增加而升高(P<0.05)。结论:TCE染毒可诱发L-02肝细胞中SET相互作用蛋白的mRNA表达水平发生改变。探讨人L-02肝细胞经三氯乙烯(TCE)染毒后SET相互作用蛋白eEF1A1、eEF1A2和DDB1 mRNA表达水平的变化。方P
目的:法:取對數生長期的L-02肝細胞,暴露于不同濃度TCE(1.0、2.0、4.0、8.0 mmol/L)中,以DMSO為溶劑對照。24 h後,採用實時熒光定量PCR檢測eEF1A1、eEF1A2和DDB1 mRNA錶達水平。結果:與對照組相比,不同濃度的TCE均能夠使L-02肝細胞eEF1A1、eEF1A2和DDB1 mRNA錶達水平髮生明顯變化。其中,DDB1和eEF1A2 mRNA錶達水平在低濃度(1.0 mmol/L)TCE暴露下顯著升高,而隨著TCE濃度的升高其mRNA錶達水平顯著降低(P<0.05或<0.01)。eEF1A1 mRNA錶達水平隨著TCE濃度的增加而升高(P<0.05)。結論:TCE染毒可誘髮L-02肝細胞中SET相互作用蛋白的mRNA錶達水平髮生改變。探討人L-02肝細胞經三氯乙烯(TCE)染毒後SET相互作用蛋白eEF1A1、eEF1A2和DDB1 mRNA錶達水平的變化。方P
목적:법:취대수생장기적L-02간세포,폭로우불동농도TCE(1.0、2.0、4.0、8.0 mmol/L)중,이DMSO위용제대조。24 h후,채용실시형광정량PCR검측eEF1A1、eEF1A2화DDB1 mRNA표체수평。결과:여대조조상비,불동농도적TCE균능구사L-02간세포eEF1A1、eEF1A2화DDB1 mRNA표체수평발생명현변화。기중,DDB1화eEF1A2 mRNA표체수평재저농도(1.0 mmol/L)TCE폭로하현저승고,이수착TCE농도적승고기mRNA표체수평현저강저(P<0.05혹<0.01)。eEF1A1 mRNA표체수평수착TCE농도적증가이승고(P<0.05)。결론:TCE염독가유발L-02간세포중SET상호작용단백적mRNA표체수평발생개변。탐토인L-02간세포경삼록을희(TCE)염독후SET상호작용단백eEF1A1、eEF1A2화DDB1 mRNA표체수평적변화。방P
OBJECTIVE:Toresearch the effects oftrichloroethylene on the RNA expressions ofSET-associated proteins including eEF1A1,eEF1A2 and DDB1 in L-02 cells.METHODS:L-02 cells,being in the logarithmic growth phase,were t reated w ith d ifferent c oncentrations (1. 0, 2. 0, 4. 0, 8. 0mmol/L) oft richloroethylene for 2 4 h ,andD MSO w ere used as control. The mRNA levels ofeEF1A1, eEF1A2 and DDB1 were analyzed with qPCR.RESULTS:The results showed that mRNA levels ofDDB1 and eEF1A2 were significantly up-regulated under low concentration oftrichloroethylene (1.0 mmol/L) and were significantly down-regulated with increasing concentrations oftrichloroethylene. The mRNA levels ofeEF1A1 were significantly up-regulated with increasing oftrichloroethylene concentration.CONCLUSION:Exposure oftrichloroethylene c ould a lter m RNA e xpression ofS ET-associated p roteins i n L -02 c ells.