Iron-induced oxidative stress modify tau phosphorylation patterns in hippocampal cell cultures

被引:104
作者
Egaña, JT
Zambrano, C
Nuñez, MT
Gonzalez-Billault, C
Maccioni, RB
机构
[1] Univ Chile, Fac Sci, Cellular & Mol Biol Lab, Santiago, Chile
[2] Univ Chile, Fac Sci, Millennium Inst Adv Studies Cell Biol & Biotechno, Lab Membrane Physiol, Santiago, Chile
关键词
Alzheimer's disease; brain hippocampal cells; Cdk5/p35; system; iron; neurodegeneration; oxidative stress; tau phosphorylation;
D O I
10.1023/A:1020727218493
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
Oxidative stress phenomena have been related with the onset of neurodegenerative diseases. Particularly in Alzheimer Disease (AD), oxygen reactive species (ROS) and its derivatives can be found in brain samples of postmortem AD patients. However, the mechanisms by which oxygen reactive species can alter neuronal function are still not elucidated. There is a growing amount of evidence pointing to a role for mitochondrial damage as the source of free radicals involved in oxidative stress. Among the species that participate in the production of oxygen reactive radicals, transition metals are one of the most important. Several reports have implicated the involvement of redox-active metals with the onset of different neurodegenerative diseases such as Alzheimer's Disease (AD), Progressive Supranuclear Palsy (PSP), Amyotrophic Lateral Sclerosis (ALS) and Parkinson's Disease (PD). On the other hand, our previous studies have indicated that Abeta-induced deregulation of the protein kinase Cdk5 associated with tau protein hyperphosphorylation constitute a critical pathway toward neurodegeneration. In the current paper we have shown that iron induces an imbalance in the function of Cdk5/p25 system of hippocampal neurons, resulting in a marked decrease in tau phosphorylation at the typical Alzheimer's epitopes. The loss of phosphorylated tau epitopes correlated with an increase in 4-hydroxy-nonenal (HNE) adducts revealing damage by oxidative stress. This effects on tau phosphorylation patterns seems to be a consequence of a decrease in the Cdk5/p25 complex activity that appears to result from a depletion of the activator p25, a mechanism in which calcium transients could be implicated.
引用
收藏
页码:215 / 223
页数:9
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