• DocumentCode
    2380365
  • Title

    PEP-1-Peroxiredoxin protein efficiently protects Raw 264.7 cells from lipopolysaccharide (LPS)-induced inflammation

  • Author

    Kim, Mi Jin ; Jeong, Hoon Jae ; Kang, Hye Won ; Kwon, Soon Won ; Woo, Su Jung ; Duk-Soo Kim ; Kwon, Hyeok Yil ; Lee, Kil Soo ; Dae Won Kim ; Park, Jinseu ; Eum, Won Sik ; Choi, Soo Young

  • Author_Institution
    Dept. of Biomed. Sci. & Res., Hallym Univ., Chunchon, South Korea
  • fYear
    2010
  • fDate
    18-18 Dec. 2010
  • Firstpage
    809
  • Lastpage
    809
  • Abstract
    It is well known that lipopolysaccharide (LPS) induces reactive oxygen species (ROS) generation and substantially enhanced inflammatory events. Peroxiredoxin (Prx) is antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. In this study, we constructed cell-permeable PEP-1-Prx fusion protein to elucidate the protective effects of Prx on inflammation in Raw 264.7 cells. PEP-1-Prx efficiently transduced into the cells and markedly inhibited LPS-induced ROS generation, cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS). In addition, PEP-1-Prx significantly reduced in the activation of mitogen-activated protein kinase (MAPK). These results indicate that PEP-1-Prx protects against LPS-induced inflammation by blocking ROS generation and MAPK, prompting the suggestion that PEP-1-Prx protein can be used as a therapeutic agent against skin inflammation.
  • Keywords
    biochemistry; cellular biophysics; enzymes; molecular biophysics; patient treatment; PEP-1-Prx fusion protein; PEP-1-peroxiredoxin protein; Raw 264.7 cells; alkyl hydroperoxides; antioxidant enzymes; cyclooxygenase-2; hydrogen peroxide; inflammation; lipopolysaccharide; mitogen-activated protein kinase; nitric oxide synthase; reactive oxygen species generation; Inflammation; Mitogen-activated protein kinase; Peroxiredoxin; Protein therapy; ROS;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedicine Workshops (BIBMW), 2010 IEEE International Conference on
  • Conference_Location
    Hong, Kong
  • Print_ISBN
    978-1-4244-8303-7
  • Electronic_ISBN
    978-1-4244-8304-4
  • Type

    conf

  • DOI
    10.1109/BIBMW.2010.5703918
  • Filename
    5703918