Alteration of iron regulatory proteins (IRP1 and IRP2) and ferritin in the brains of scrapie-infected mice

被引:27
作者
Kim, Boe-Hyun
Jun, Yong-Chul
Jin, Jae-Kwang
Kim, Jae-Il
Kim, Nam-Ho
Leibold, Elizabeth A.
Connor, James R.
Choi, Eun-Kyoung
Carp, Richard I.
Kim, Yong-Sun
机构
[1] Hallym Univ, Coll Med, Dept Microbiol, Kyonggi Do 431060, South Korea
[2] Hallym Univ, Acad Sci, Ilsong Inst Life Sci, Kyonggi Do, South Korea
[3] New York State Inst Basic Res Dev Disabil, Staten Isl, NY 10314 USA
[4] Univ Utah, Dept Med, Salt Lake City, UT 84112 USA
[5] Univ Utah, Eccles Program Human Mol Biol & Genet, Salt Lake City, UT 84112 USA
[6] Penn State Univ, Coll Med, GM Leader Family Lab Alzheimers Dis Res, Dept Neurosurg, Hershey, PA USA
关键词
transmissible spongiform encephalopathies (TSEs); oxidative stress; neurodegeneration; iron regulatory proteins (IRPs); ferritin; Astrocytosis;
D O I
10.1016/j.neulet.2007.05.061
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Considerable evidence suggests that oxidative stress may be involved in the pathogenesis of Transmissible Spongiform Encephalopathies (TSEs). To investigate the involvement of iron metabolism in TSEs, we examined the expression levels of iron regulatory proteins (IRPs), ferritins, and binding activities of IRPs to iron-responsive element (IRE) in scrapie-infected mice. We found that the IRPs-IRE-binding activities and ferritins were increased in the astrocytes of hippocampus and cerebral cortex in the brains of scrapie-infected mice. These results suggest that alteration of iron metabolism contributes to development of neurodegeneration and that some protective mechanisms against iron-induced oxidative damage may occur during the pathogenesis of TSEs. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:158 / 163
页数:6
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