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细胞周期蛋白依赖性激酶5(cdk-5)过表达对大鼠tau蛋白磷酸化及空间记忆的影响。

The effect of cdk-5 overexpression on tau phosphorylation and spatial memory of rat.

作者信息

Liao Xiaomei, Zhang Yingchun, Wang Yipeng, Wang Jianzhi

机构信息

Department of Pathophysiology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

Sci China C Life Sci. 2004 Jun;47(3):251-7. doi: 10.1007/BF03182770.

Abstract

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.

摘要

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。

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