Shah Kavita, Lahiri Debomoy K
Department of Chemistry and Purdue University Center for Cancer Research, 560 Oval Drive, West Lafayette, IN, 47907, USA.
Departments of Psychiatry and Medical & Molecular Genetics, Institute of Psychiatric Research, Neuroscience Research Center, Indiana University School of Medicine, 320 W. 15th Street, Indianapolis, IN, 46202-2266, USA.
Mol Neurobiol. 2017 Apr;54(3):2255-2268. doi: 10.1007/s12035-016-9792-7. Epub 2016 Mar 5.
Cdk5, a cyclin-dependent kinase family member, is a global orchestrator of neuronal cytoskeletal dynamics. During embryogenesis, Cdk5 is indispensable for brain development. In adults, it is essential for numerous neuronal processes, including higher cognitive functions such as learning and memory formation, drug addiction, pain signaling, and long-term behavior changes through long-term potentiation and long-term depression, all of which rely on rapid alterations in the cytoskeleton. Cdk5 activity becomes deregulated in various brain disorders, including Alzheimer's disease, Parkinson's disease, Huntington's disease, attention-deficit hyperactivity disorder, epilepsy, schizophrenia, and ischemic stroke; these all result in profound remodeling of the neuronal cytoskeleton. This Commentary specifically focuses on the pleiotropic contribution of Cdk5 in regulating neuronal microtubule remodeling. Because the vast majority of the physiological substrates of Cdk5 are associated with the neuronal cytoskeleton, our emphasis is on the Cdk5 substrates, such as CRMP2, stathmin, drebrin, dixdc1, axin, MAP2, MAP1B, doublecortin, kinesin-5, and tau, that have allowed to unravel the molecular mechanisms through which Cdk5 exerts its divergent roles in regulating neuronal microtubule dynamics, both in healthy and disease states.
细胞周期蛋白依赖性激酶5(Cdk5)是细胞周期蛋白依赖性激酶家族成员,是神经元细胞骨架动力学的全局协调者。在胚胎发育过程中,Cdk5对大脑发育不可或缺。在成体中,它对众多神经元过程至关重要,包括学习和记忆形成等高级认知功能、药物成瘾、疼痛信号传导以及通过长时程增强和长时程抑制实现的长期行为改变,所有这些都依赖于细胞骨架的快速改变。在包括阿尔茨海默病、帕金森病、亨廷顿病、注意力缺陷多动障碍、癫痫、精神分裂症和缺血性中风在内的各种脑部疾病中,Cdk5活性失调;这些疾病都会导致神经元细胞骨架的深刻重塑。本述评特别关注Cdk5在调节神经元微管重塑中的多效性作用。由于Cdk5的绝大多数生理底物都与神经元细胞骨架相关,我们重点关注Cdk5的底物,如CRMP2、stathmin、drebrin、dixdc1、axin、微管相关蛋白2(MAP2)、微管相关蛋白1B(MAP1B)、双皮质素、驱动蛋白-5和微管相关蛋白tau,这些底物有助于揭示Cdk5在健康和疾病状态下调节神经元微管动力学时发挥其不同作用的分子机制。