Activation of MKK6, an upstream activator of p38, in Alzheimer's disease

被引:124
|
作者
Zhu, XW
Rottkamp, CA
Hartzler, A
Sun, Z
Takeda, A
Boux, H
Shimohama, S
Perry, G
Smith, MA
机构
[1] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Nutr, Cleveland, OH 44106 USA
[3] Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 980, Japan
[4] StressGen Biotechnol Corp Inc, Victoria, BC, Canada
[5] Kyoto Univ, Fac Med, Dept Neurol, Kyoto 606, Japan
关键词
Alzheimer's disease; cell cycle; mitogen-activated protein kinase kinase 6; oxidative stress; p38;
D O I
10.1046/j.1471-4159.2001.00597.x
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
Mitogen-activated protein kinase (MAPK) p38 has been implicated in the pathogenesis of Alzheimer's disease, but the upstream cascade leading to p38 activation has not been elucidated in the disease. In the present study, we focused on mitogen-activated protein kinase kinase 6 (MKK6), one of the upstream activators of p38 MAPK. We found that MKK6 was not only increased but also specifically associated with granular structures in the susceptible neurons in the hippocampus and cortex of Alzheimer's disease patients, but was only weakly diffuse in the cytoplasm in neurons in control cases. Immunoblot analysis demonstrated a significant increase of MKK6 level in Alzheimer's disease compared with age-matched controls. In this regard, in hippocampal and cortical regions of individuals with Alzheimer's disease, the activated phospho-MKK6 was localized exclusively in association with pathological alterations including neurofibrillary tangles, senile plaques, neuropil threads and granular structures, overlapping with activated p38 MAPK suggesting both a functional and mechanic link. By immunoblot analysis, phospho-MKK6 is also significantly increased in AD compared with control cases. Together, these findings lend further credence to the notion that the p38 MAPK pathway is dysregulated in Alzheimer's disease and also indicates an active role for this pathway in disease pathogenesis.
引用
收藏
页码:311 / 318
页数:8
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