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X线修复交叉互补基因1对氢醌致人支气管上皮细胞DNA损伤的保护作用

方道奎 何云 张建清 胡大林 沙焱 庄志雄

中国药理学与毒理学杂志2009,Vol.23Issue(2):89-98,10.
中国药理学与毒理学杂志2009,Vol.23Issue(2):89-98,10.DOI:10.3867/j.issn.1000-3002.2009.02.002

X线修复交叉互补基因1对氢醌致人支气管上皮细胞DNA损伤的保护作用

X-ray repair cross complementing group 1 protects human bronchial epithelial cells from hydroquinone-induced DNA damage

方道奎 1何云 2张建清 1胡大林 3沙焱 4庄志雄1

作者信息

  • 1. 深圳市疾病预防控制中心,广东,深圳,518020
  • 2. 中山大学公共卫生学院,广东,广州,510080
  • 3. 佛山大学医学院,广东,佛山,528000
  • 4. 深圳市职业病防治院,广东,深圳,518001
  • 折叠

摘要

Abstract

AIM To explore the molecular mechanism of hydroquinone genotoxicity in human bronchial epithelial cells and investigate whether human X-ray repair cross complementing group 1 (XRCC1)was involved in protecting cells from the damage caused by hydroquinone. METHODS XRCC1 gene was knocked down by RNA interference and XRCC1-deficient cell was established by transfected recombinant plasmid pEGFP-C1-pU6-dsRNA. Normal human bronchial epithelial cells (normal cells) and cells transfected with the empty vector of pEGFP-C1 (vector cells) were used as the normal control and vector control. All cells were treated with different concentrations of hydroquinone (10-100 μmol·L-1) for 4 h. MTT assay was used to test cell viability and comet assay was used to detect the DNA damage and repairment. RESULTS MTT assay showed that hydroquinone inhibited the growth of cells in a concentration-dependant manner and the survival number of XRCC1-deficient cell was less than that of the two control groups. Comet assay revealed that different concentrations of hydroquinone caused more severe DNA damage in XRCC1-deficient cell line than in control cells and there were no significant difference in the two control groups. CONCLUSION The results suggest XRCC1 be involved in preventing cells from damage caused by hydroquinone.

关键词

X线修复交叉互补基因1/毒性/氢醌/上皮细胞,支气管,人

Key words

X-ray repair cross complementing 1/toxicity/hydroquinone/epithelial cells, bronchial, human

分类

医药卫生

引用本文复制引用

方道奎,何云,张建清,胡大林,沙焱,庄志雄..X线修复交叉互补基因1对氢醌致人支气管上皮细胞DNA损伤的保护作用[J].中国药理学与毒理学杂志,2009,23(2):89-98,10.

基金项目

国家重点基础研究发展计划资助项目(2002CB512904) (2002CB512904)

国家自然科学基金资助项目(39970636) (39970636)

The project supported by National Basic Research Program of China(2002CB512904) (2002CB512904)

and National Natural Science Foundation of China(39970636) (39970636)

中国药理学与毒理学杂志

OA北大核心CSCDCSTPCD

1000-3002

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