Involvement of cyclin dependent kinase5 activator p25 on tau phosphorylation in mouse brain

被引:68
作者
Takashima, A
Murayama, M
Yasutake, K
Takahashi, H
Yokoyama, M
Ishiguro, K
机构
[1] RIKEN, Brain Sci Inst, Lab Alzheimers Dis, Wako, Saitama 3510198, Japan
[2] Mitsubishi Kasei Inst Life Sci, Tokyo, Japan
关键词
cyclin dependent kinase5; p25; tau; Alzheimer's disease; neurofibrillary tangles;
D O I
10.1016/S0304-3940(01)01864-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
P35 or its truncated fragment p25 is required for cyclin dependent kinase (Cdk)5 activation. It has been reported that p25 is accumulated in the brain of Alzheimer's disease (AD) patients and that p25/Cdk5 induces high phosphorylation of tau and apoptosis in cultured neurons (Nature 402 (1999) 615). Our investigation of AD brain did not show specific accumulation of p25. Exposure to Ca ionophore (A23187) at 10(-6) M induced p25 accumulation in rat primary hippocampal neurons, causing neuronal death without showing hyperphosphorylation of tau. Transgenic mice expressing p25 showed the accumulation of p25 but neither hyperphosphorylation of tau nor neuronal death was shown in these mice. The feature of these mice was the progression of cell growth in pituitary gland. These results suggest that over-expression of p25 lead to the activation of cell cycle but not to the direct phosphorylation of tau. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:37 / 40
页数:4
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