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中国仓鼠肺成纤维细胞和HeLa细胞DNA氧化损伤的自身修复能力与比较
引用本文:李明正,金中初,陈维亚,李红娟.中国仓鼠肺成纤维细胞和HeLa细胞DNA氧化损伤的自身修复能力与比较[J].浙江大学学报(医学版),2004,33(3):235-238.
作者姓名:李明正  金中初  陈维亚  李红娟
作者单位:1. 浙江大学医学院,浙江,杭州,310031
2. 杭州师范学院医学院,浙江,杭州,310012
基金项目:国家自然科学基金,浙江省自然科学基金
摘    要:目的:研究不同氧化相关因素对中国仓鼠肺成纤维细胞(CHL)和HeLa细胞DNA损伤的自身修复情况.方法:将CHL细胞和HeLa细胞用不同氧化相关因素处理一定时间CHL细胞:过氧化氢(H2O2)25 min,重铬酸钾(K2Cr2O7)105 min,阿霉素(Dox)75 min;HeLa细胞:H2O2 25 min,K2Cr2O7 105 min],随后立即去毒培养0、0.5、1、2、3 h,以碱性单细胞凝胶电泳技术检测DNA链断裂情况.结果:①CHL细胞经H2O2、K2Cr2O7、Dox作用后引起DNA链断裂,去毒培养1 h链断裂修复明显(P<0.01);去毒培养2~3 h,前两毒剂的损伤组完全修复,而Dox组链断裂仍高于未损伤组;②HeLa细胞经H2O2、K2Cr2O7作用后引起DNA链断裂,去毒培养0.5 h链断裂明显修复(P<0.01),去毒培养1 h则完全修复;③CHL细胞和HeLa细胞损伤后修复的拖尾率与修复时间的回归系数显著不同(P<0.05).结论:两种细胞在氧化性DNA损伤后均迅速启动自身修复,但HeLa细胞比CHL细胞有更快的修复能力;同时这两种细胞由Dox所致损伤修复能力均较H2O2、K2Cr2O7所致的差.

关 键 词:成纤维细胞/病理学  Hela细胞/病理学  DNA链断裂  DNA修复  过氧化氢/毒性  重铬酸钾/毒性  阿霉素/毒性  仓鼠
文章编号:1008-9292(2004)03-0235-04
修稿时间:2002年4月24日

DNA repair of CHL cells and HeLa cells after DNA damage induced by different oxidative agents
LI Ming-zheng,JIN Zhong-chu,CHEN Wei-ya,et al.DNA repair of CHL cells and HeLa cells after DNA damage induced by different oxidative agents[J].Journal of Zhejiang University(Medical Sciences),2004,33(3):235-238.
Authors:LI Ming-zheng  JIN Zhong-chu  CHEN Wei-ya  
Institution:College of Medicine, Zhejiang University, Hangzhou 310031, China.
Abstract:OBJECTIVE: To investigate DNA repair in CHL cells and HeLa cells after DNA damage induced by different oxidative agents. METHODS: CHL cells and HeLa cells were exposed to various damaging agents, CHL cells: H(2)O(2) for 25 min, K(2)Cr(2)O(7) for 105 min, doxorubicin (Dox) for 75 min HeLa cells: H(2)O(2) for 25 min, K(2)Cr(2)O(7) for 105 min; then cells were continuously cultured for 0-3 h after washing. Alkaline single cell gel electrophoresis (ASCGE) assay was used to detect DNA strand breaks. RESULT: (1) DNA strand breaks were induced in CHL cells after exposure to H(2)O(2) K(2)Cr(2)O(7) or Dox, which were repaired evidently after continuous culture for 1 h(P<0.01). The damages induced by H(2)O(2) or K(2)Cr(2)O(7) were repaired completely after culture for 2-3 h. However, the demage induced by Dox was repaired incompletely. (2) DNA strand breaks were induced also in HeLa cells after exposure to H(2)O(2) or K(2)Cr(2)O(7), which were repaired evidently after continuous culture for 0.5 h(P<0.01),and completely after culture for 1 h. (3) The regression coefficient related to the rate of comet cells and repair time was statistically different (P<0.05) between CHL cells and HeLa cells. CONCLUSION: DNA damage induced by Dox is repaired more difficult than that induced by H(2)O(2) or K(2)Cr(2)O(7). The repair initiates immediately after DNA damage in both of cells, but more rapidly in HeLa cells than in CHL cells.
Keywords:Fibroblasts/pathol  HeLa cells/pathol  DNA strand breaks  DNA repair  Hydrogen peroxide/tox  Potassium dichromate/tox  Doxorubicin/ tox  Hamsters
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