Liao Xiaomei, Zhang Yingchun, Wang Yipeng, Wang Jianzhi
Department of Pathophysiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Sci China C Life Sci. 2004 Jun;47(3):251-7. doi: 10.1007/BF03182770.
In Alzheimer's disease (AD), hyperphosphorylation of tau may be the underlying mechanism for the cytoskeletal abnormalities and neuronal death. It was reported that cyclin-dependent kinase5 (cdk-5) could phosphorylate tau at most AD-related epitopes in vitro. In this study, we investigated the effect of cdk-5 overexpression on tau phosphorylation and spatial memory in rat. We demonstrated that 24 h after transfection into rat hippocampus, cdk-5 was overexpressed and induced a reduced staining with antibody tau-1 and an enhanced staining with antibodies 12e8 and PHF-1, suggesting hyperphosphorylation of tau at Ser199/202, Ser262/356 and Ser396/404 sites. Additionally, the cdk-5 transfected rats showed long latency to find the hidden platform in Morris water maze compared to the control rat. 48 h after transfection, the level of cdk-5 was decreased significantly, and the latency of rats to find the hidden platform was prolonged. It implies that in vivo overexpression of cdk-5 leads to impairment of spatial memory in rat and tau hyperphosphorylation may be the underlying mechanism.
在阿尔茨海默病(AD)中,tau蛋白的过度磷酸化可能是细胞骨架异常和神经元死亡的潜在机制。据报道,细胞周期蛋白依赖性激酶5(cdk-5)在体外可使tau蛋白在大多数与AD相关的表位发生磷酸化。在本研究中,我们调查了cdk-5过表达对大鼠tau蛋白磷酸化和空间记忆的影响。我们证明,将其转染到大鼠海马体24小时后,cdk-5过表达,并导致tau-1抗体染色减少,而12e8和PHF-1抗体染色增强,这表明tau蛋白在Ser199/202、Ser262/356和Ser396/404位点发生了过度磷酸化。此外,与对照大鼠相比,转染cdk-5的大鼠在莫里斯水迷宫中找到隐藏平台的潜伏期较长。转染48小时后,cdk-5水平显著下降,大鼠找到隐藏平台的潜伏期延长。这意味着体内cdk-5过表达会导致大鼠空间记忆受损,tau蛋白过度磷酸化可能是其潜在机制。