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Increased susceptibility of MER5 (peroxiredoxin III) knockout mice to LPS-induced oxidative stress
被引:131
作者:
Li, Lianqin
Shoji, Wataru
Takano, Hirohisa
Nishimura, Noriko
Aoki, Yasunobu
Takahashi, Ryoya
Goto, Sataro
Kaifu, Tomonori
Takai, Toshiyuki
Obinata, Masuo
机构:
[1] Tohoku Univ, Dept Cell Biol, Inst Dev Aging & Canc, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Natl Inst Environm Studies, Endocrine Disruptors & Dioxin Res Project, Tsukuba, Ibaraki, Japan
[3] Natl Inst Environm Studies, Environm Hlth Sci Div, Tsukuba, Ibaraki, Japan
[4] Natl Inst Environm Studies, Res Ctr Environm Risk, Tsukuba, Ibaraki, Japan
[5] Toho Univ, Sch Pharmaceut Sci, Dept Biochem, Tokyo, Japan
关键词:
oxidative stress;
reactive oxygen species (ROS);
lung inflammation;
peroxiredoxin;
MER5 (peroxiredoxin III);
D O I:
10.1016/j.bbrc.2007.02.022
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
MER5 (also called peroxiredoxin III, PrxIII) is a member of peroxircdoxin family that has antioxidant activity. The present study was performed to investigate its in vivo function using MER5 knockout mice. MER5 knockout mice were born in normal frequency and could grow to maturity, but we found that intracellular ROS levels are significantly higher in the macrophages of the knockout mice. We examined roles of MER5 function for the oxidative stress responses by intratracheal inoculation of lipopolysaccharide (LPS) to the mice. Lung inflammation such as inflammatory cell infiltration and airway wall thickening was more severely detected in the knockout mice. At the same time, oxidative damage on DNA and proteins was more strongly detected in lung tissues of the knockout mice, including 8-hydroxy-2'-deoxyguanosine (8-OHdG) formation and protein carbonylation. The degrees of lung inflammation and oxidative damage were positively related with LPS doses. Our results indicate that MER5 knockout mice accumulated higher intracellular ROS levels, which cause I-PS-induced lung injury more severely, and thus, Suggested that MER5 acts as an important scavenger of reactive oxygen species (ROS) under oxidative stress. (c) 2007 Elsevier Inc. All rights reserved.
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页码:715 / 721
页数:7
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