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
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;
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
DOI :
10.1109/BIBMW.2010.5703918