ZUO Ya-hui,WANG Fang,WANG Xiao-li,LI Jian-guo,WANG Zhong-wen,TONG Jian.Proteomics study of progeny of normal human liver cells irradiated by 60Co γ-rays[J].Chinese Journal of Radiological Medicine and Protection,2009,29(4):389-392
Proteomics study of progeny of normal human liver cells irradiated by 60Co γ-rays
Received:April 24, 2009  
DOI:
KeyWords:Human liver cell  Proteomics  Two-dimensional electrophoresis  Mass spectrometry  Genomic instability
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Author NameAffiliationE-mail
ZUO Ya-hui China Institute for Radiation Protection, Taiyuan 030006, China  
WANG Fang China Institute for Radiation Protection, Taiyuan 030006, China  
WANG Xiao-li China Institute for Radiation Protection, Taiyuan 030006, China  
LI Jian-guo China Institute for Radiation Protection, Taiyuan 030006, China  
WANG Zhong-wen 中国原子能科学研究院  
TONG Jian 苏州大学放射医学与公共卫生学院 tongjian@suda.edu.cn 
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Abstract::
      Objective To characterize the differential protein expression in the progeny of human liver cells surviving from ionizing radiation by the proteomic analysis. Methods Two-dimensional electrophoresis gel coupled with mass spectrometry was used to explore the specific protein expression in the progeny of 7702 human liver cells surviving from ionizing radiation. Alterations in expression level of protein spots between the control and the progeny groups were statistically analyzed by ImageMaster 2D Platinum software and mass spectrometry was used to identify the protein spots with significantly altered expression-level. Results The progeny of irradiated cells were derived from human liver cell line exposed to 0, 2, 4, 6 Gy of 60Co γ-irradiation. A total of 42 differentially expressed proteins between the control and the progeny of the irradiated cells groups were screened, of which 17 were identified by matrix assistant laser desorption ion-top off light-mass spectrometry (MALDI-TOF-MS) analysis, including 4 up-regulated and 13 down-regulated proteins. Conclusions The differentially expressed proteins profile could be significantly altered in the progeny of irradiated cells. The proteomics approach has the potential to detect the protein changes relevant to radiation-induced genomic instability(RIGI). Further study of differentially expressed proteins would likely reveal the molecular mechanisms of gene expression in RIGI.
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