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DU Bin-bin, LIU Qing, ZHANG Wei-sheng, WANG Xiao-yan, JIA Pen-fei, WANG Xiao-hu, LI Sha, YANG Xiong-fei, ZHANG Hong, Guo Tian-kang, #. Role of NADPH Oxidase in HeLa Cell Lesion Induced by Xray Irradiation[J]. Nuclear Physics Review, 2008, 25(4): 391-396. doi: 10.11804/NuclPhysRev.25.04.391
Citation: DU Bin-bin, LIU Qing, ZHANG Wei-sheng, WANG Xiao-yan, JIA Pen-fei, WANG Xiao-hu, LI Sha, YANG Xiong-fei, ZHANG Hong, Guo Tian-kang, #. Role of NADPH Oxidase in HeLa Cell Lesion Induced by Xray Irradiation[J]. Nuclear Physics Review, 2008, 25(4): 391-396. doi: 10.11804/NuclPhysRev.25.04.391

Role of NADPH Oxidase in HeLa Cell Lesion Induced by Xray Irradiation

doi: 10.11804/NuclPhysRev.25.04.391
  • Received Date: 1900-01-01
  • Rev Recd Date: 1900-01-01
  • Publish Date: 2008-12-20
  • To investigate the role of NADPH oxidase in HeLa cell lesion induced by Xray irradiation, the change of cell survival was detected with MTT assay, reactive oxygen species (ROS) was measured by fluorospectrophotometer. Immunostaining and confocal laserscanning microscopy was employed to detect the colocalization of two subunit of NADPH oxidase, p47phox and gp91phox in the cell. Western blotting was used to detect the expression of gp91phox before and after Xray irradiation. After Xray irradiation, intracellular level of ROS increased obviously. But the increase could be blocked by diphenyleneiodonium (DPI), an inhibitor of NADPH oxidase. Meanwhile, cytosolic subunit p47phox moved to membrane and colocalizated with gp91phox after
    irradiation. Moreover, the results also show that gp91phox increased sharply after 12 Gy Xray irradiation. Therefore, NADPH oxidasemediated production of ROS plays an important role in HeLa cell lesion induced by Xray.
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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Role of NADPH Oxidase in HeLa Cell Lesion Induced by Xray Irradiation

doi: 10.11804/NuclPhysRev.25.04.391

Abstract: To investigate the role of NADPH oxidase in HeLa cell lesion induced by Xray irradiation, the change of cell survival was detected with MTT assay, reactive oxygen species (ROS) was measured by fluorospectrophotometer. Immunostaining and confocal laserscanning microscopy was employed to detect the colocalization of two subunit of NADPH oxidase, p47phox and gp91phox in the cell. Western blotting was used to detect the expression of gp91phox before and after Xray irradiation. After Xray irradiation, intracellular level of ROS increased obviously. But the increase could be blocked by diphenyleneiodonium (DPI), an inhibitor of NADPH oxidase. Meanwhile, cytosolic subunit p47phox moved to membrane and colocalizated with gp91phox after
irradiation. Moreover, the results also show that gp91phox increased sharply after 12 Gy Xray irradiation. Therefore, NADPH oxidasemediated production of ROS plays an important role in HeLa cell lesion induced by Xray.

DU Bin-bin, LIU Qing, ZHANG Wei-sheng, WANG Xiao-yan, JIA Pen-fei, WANG Xiao-hu, LI Sha, YANG Xiong-fei, ZHANG Hong, Guo Tian-kang, #. Role of NADPH Oxidase in HeLa Cell Lesion Induced by Xray Irradiation[J]. Nuclear Physics Review, 2008, 25(4): 391-396. doi: 10.11804/NuclPhysRev.25.04.391
Citation: DU Bin-bin, LIU Qing, ZHANG Wei-sheng, WANG Xiao-yan, JIA Pen-fei, WANG Xiao-hu, LI Sha, YANG Xiong-fei, ZHANG Hong, Guo Tian-kang, #. Role of NADPH Oxidase in HeLa Cell Lesion Induced by Xray Irradiation[J]. Nuclear Physics Review, 2008, 25(4): 391-396. doi: 10.11804/NuclPhysRev.25.04.391

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