癌变·畸变·突变
癌變·畸變·突變
암변·기변·돌변
CARCINOGENSES,TERATOGENSIS AND MUTAGENESIS
2014年
1期
24-29
,共6页
柯跃斌%黄娟%朱舟%吴双%陶功华
柯躍斌%黃娟%硃舟%吳雙%陶功華
가약빈%황연%주주%오쌍%도공화
甲醛%DNA氧化%DNA甲基化%8-羟基鸟嘌呤脱氧核苷%5-甲基胞嘧啶
甲醛%DNA氧化%DNA甲基化%8-羥基鳥嘌呤脫氧覈苷%5-甲基胞嘧啶
갑철%DNA양화%DNA갑기화%8-간기조표령탈양핵감%5-갑기포밀정
formaldehyde%DNA methylation%DNA oxidation%8-oxo-dG%5-mC
目的:分析甲醛染毒对体外培养的人Ⅱ型肺泡上皮细胞(A549)内8-羟基鸟嘌呤脱氧核苷(8-oxo-dG)水平、DNA 5-甲基胞嘧啶(5-mC)含量的影响及其时间-效应和剂量-效应关系,探讨甲醛所致的细胞DNA氧化与DNA甲基化的关联性。方法:用5~20μmol/L甲醛作用于A549细胞,用高压液相色谱串联电化学检测技术分析细胞DNA 8-oxo-dG水平,用免疫荧光和高效毛细管电泳法检测细胞全基因组DNA 5-mC含量改变。结果:甲醛染毒提高了细胞8-oxo-dG水平,但是降低了细胞的DNA 5-mC含量。甲醛致细胞DNA氧化与DNA甲基化呈现不同特点,A549细胞暴露于20μmol/L甲醛后,DNA氧化水平在1周甚至更早时间就已显著增高,而相同条件下DNA甲基化水平的改变需要6周以上的时间,DNA甲基化的改变滞后于DNA氧化。A549细胞经5~20μmol/L甲醛染毒8周后,DNA氧化水平与甲醛剂量呈正相关关系,而同样条件下DNA甲基化水平与甲醛剂量呈负相关关系。结论:甲醛染毒可提高DNA氧化水平,降低细胞DNA甲基化水平。在甲醛的毒作用效应中,细胞DNA氧化损伤可能是早于其DNA甲基化的一个重要分子事件。
目的:分析甲醛染毒對體外培養的人Ⅱ型肺泡上皮細胞(A549)內8-羥基鳥嘌呤脫氧覈苷(8-oxo-dG)水平、DNA 5-甲基胞嘧啶(5-mC)含量的影響及其時間-效應和劑量-效應關繫,探討甲醛所緻的細胞DNA氧化與DNA甲基化的關聯性。方法:用5~20μmol/L甲醛作用于A549細胞,用高壓液相色譜串聯電化學檢測技術分析細胞DNA 8-oxo-dG水平,用免疫熒光和高效毛細管電泳法檢測細胞全基因組DNA 5-mC含量改變。結果:甲醛染毒提高瞭細胞8-oxo-dG水平,但是降低瞭細胞的DNA 5-mC含量。甲醛緻細胞DNA氧化與DNA甲基化呈現不同特點,A549細胞暴露于20μmol/L甲醛後,DNA氧化水平在1週甚至更早時間就已顯著增高,而相同條件下DNA甲基化水平的改變需要6週以上的時間,DNA甲基化的改變滯後于DNA氧化。A549細胞經5~20μmol/L甲醛染毒8週後,DNA氧化水平與甲醛劑量呈正相關關繫,而同樣條件下DNA甲基化水平與甲醛劑量呈負相關關繫。結論:甲醛染毒可提高DNA氧化水平,降低細胞DNA甲基化水平。在甲醛的毒作用效應中,細胞DNA氧化損傷可能是早于其DNA甲基化的一箇重要分子事件。
목적:분석갑철염독대체외배양적인Ⅱ형폐포상피세포(A549)내8-간기조표령탈양핵감(8-oxo-dG)수평、DNA 5-갑기포밀정(5-mC)함량적영향급기시간-효응화제량-효응관계,탐토갑철소치적세포DNA양화여DNA갑기화적관련성。방법:용5~20μmol/L갑철작용우A549세포,용고압액상색보천련전화학검측기술분석세포DNA 8-oxo-dG수평,용면역형광화고효모세관전영법검측세포전기인조DNA 5-mC함량개변。결과:갑철염독제고료세포8-oxo-dG수평,단시강저료세포적DNA 5-mC함량。갑철치세포DNA양화여DNA갑기화정현불동특점,A549세포폭로우20μmol/L갑철후,DNA양화수평재1주심지경조시간취이현저증고,이상동조건하DNA갑기화수평적개변수요6주이상적시간,DNA갑기화적개변체후우DNA양화。A549세포경5~20μmol/L갑철염독8주후,DNA양화수평여갑철제량정정상관관계,이동양조건하DNA갑기화수평여갑철제량정부상관관계。결론:갑철염독가제고DNA양화수평,강저세포DNA갑기화수평。재갑철적독작용효응중,세포DNA양화손상가능시조우기DNA갑기화적일개중요분자사건。
OBJECTIVE: To explore the potential association of formaldehyde (FA)-induced cellular DNA oxidation and DNA methylation. 8-oxo-7,8-dihydroguanine (8-oxo-dG) levels and DNA 5-mC content were analyzed after FA exposure in human alveolar typeⅡepithelial (A549) cells in vitro,and their time-dose-effect were also analyzed. METHODS:A549 cells were exposed to 5-20μmol/L FA. 8-oxo-dG levels of cellular DNA were measured by high pressure liquid chromatography with electrochemical detection,alterations of genomic DNA methylation levels were investigated by immunofluorescence and high performance capillary electrophoresis. RESULTS:The levels of 8-oxo-dG in A549 cells were increased after FA exposure,but cellular DNA 5-mC content is reduced. There were different characteristics in FA -induced cellular DNA oxidation and DNA methylation. After exposure to 20 μmol/L FA, DNA oxidation levels of A549 cells had increased significantly in 1 week and even earlier. However,it took at least 6 weeks for significant changes in the level of DNA methylation under the same conditions. After exposed to 5-20μmol/L FA for 8 weeks,a positive correlation was found between the dose of FA and DNA oxidation levels in A549 cells,but the DNA methylation levels were negatively correlated with the dose of FA under the same conditions. CONCLUSION:After FA exposure,oxidative DNA damage in A549 cells was increased but DNA methylation decreased. In the cytotoxicity effect of FA,oxidative DNA damage might be an earlier important molecular event than DNA methylation.