• DocumentCode
    2508330
  • Title

    Exposure of Hela Cells to Serum Results in Increased Cellular Thiol Concentration and Formaldehyde-Induced DNA-Protein Crosslink

  • Author

    Xiao Lin ; Liang Si-Si ; Chang Qing ; Fu Cong ; Yang Xu

  • Author_Institution
    Coll. of Life Sci., Huazhong Normal Univ., Wuhan, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    How does inhaled formaldehyde transfer the genotoxicity from exposure organ to site distant organs via blood? This is the key question to understand leukemia induced by formaldehyde. To answer this question, we used new born calf serum (NBS) as "blood" and Hela cells as materials to investigate its effects on cellular thiol concentration and DNA-protein crosslink (DPC) induced by formaldehyde. Our results showed that when new born calf serum (NBS) were absent, 250 mumolldrL-1 formaldehyde induced relatively low amount of DPC, while cellular thiol concentration was also low. In contrast, DPC formation and cellular thiol concentration were significantly elevated in the presence of 1% and 10% NBS (p<0.01, p<0.05). These results indicated that NBS could regenerate cellular thiol concentration and stimulate DPC formation as a consequence in formaldehyde exposed cells. This effect may provide a basis for the understanding of site distant toxicity of formaldehyde and to explain whether inhaled formaldehyde could induce leukemia.
  • Keywords
    DNA; biological organs; blood; cancer; cellular biophysics; genetics; molecular biophysics; proteins; toxicology; tumours; Hela cell exposure; blood; cellular thiol concentration; formaldehyde-induced DNA-protein crosslink; genotoxicity; leukemia; new born calf serum; Amino acids; Biochemistry; Biological materials; Blood; Cancer; Cells (biology); Joining processes; Liver; Mice; NIST;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5162829
  • Filename
    5162829