Fischer André, Sananbenesi Farahnaz, Spiess Joachim, Radulovic Jelena
Laboratory on Cell Biologic Mechanisms of Memory, Department of Molecular Neuroendocrinology, Max Planck Institute for Experimental Medicine, Goettingen, Germany.
Curr Drug Targets CNS Neurol Disord. 2003 Dec;2(6):375-81. doi: 10.2174/1568007033482706.
Cyclin-dependent kinase 5 (Cdk5), a Ser/Thr kinase, regulates the phosphorylation of neuronal proteins and thereby influences neuronal morphology, migration and axon growth. Tightly coordinated interactions between Cdk5 and its activator proteins p35 and p39 are critical for the developmental processes of post-mitotic neurons as well as functioning of the adult CNS. Excessive up-regulation of Cdk5 activity leading to hyperphosphorylation of cytoskeletal proteins has been linked to neurodegenerative disorders, such as Alzheimer's disease (AD). On this basis it was proposed that Cdk5 might be a promising drug target. The physiologic role of Cdk5 in the adult CNS has been addressed recently. It was demonstrated that Cdk5 is involved in striatal and hippocampal neuronal plasticity and long-term behavioral changes associated with these processes. On the basis of the newly identified role of Cdk5 in synaptic plasticity, learning and memory the view that Cdk5 represents a good drug target in AD accompanied by cognitive dysfunctions may have to be revisited. Alternatively, targeting the mechanisms up-stream of Cdk5 leading to deregulation of Cdk5 activity, such as proteolytic cleavage of its activating subunits may prove to be more beneficial as a therapeutical approach.
细胞周期蛋白依赖性激酶5(Cdk5)是一种丝氨酸/苏氨酸激酶,可调节神经元蛋白的磷酸化,从而影响神经元形态、迁移和轴突生长。Cdk5与其激活蛋白p35和p39之间紧密协调的相互作用对于有丝分裂后神经元的发育过程以及成体中枢神经系统的功能至关重要。Cdk5活性的过度上调导致细胞骨架蛋白的过度磷酸化,这与神经退行性疾病如阿尔茨海默病(AD)有关。基于此,有人提出Cdk5可能是一个有前景的药物靶点。最近人们已经探讨了Cdk5在成体中枢神经系统中的生理作用。研究表明,Cdk5参与纹状体和海马神经元的可塑性以及与这些过程相关的长期行为变化。基于Cdk5在突触可塑性、学习和记忆方面新发现的作用,认为Cdk5是伴有认知功能障碍的AD的良好药物靶点这一观点可能需要重新审视。或者,针对导致Cdk5活性失调的Cdk5上游机制,如其激活亚基的蛋白水解切割,可能作为一种治疗方法被证明更有益。