Fu Amy K Y, Ip Nancy Y
Department of Biochemistry, Biotechnology Research Institute and Molecular Neuroscience Center, Hong Kong University of Science and Technology, Hong Kong, China.
Cell Adh Migr. 2007 Apr-Jun;1(2):110-2. doi: 10.4161/cam.1.2.4617. Epub 2007 Apr 21.
Emerging evidence has indicated a regulatory role of cyclin-dependent kinase 5 (Cdk5) in synaptic plasticity as well as in higher brain functions, such as learning and memory. However, the molecular and cellular mechanisms underlying the actions of Cdk5 at synapses remain unclear. Recent findings demonstrate that Cdk5 regulates dendritic spine morphogenesis through modulating actin dynamics. Ephexin1 and WAVE-1, two important regulators of the actin cytoskeleton, have both been recently identified as substrates for Cdk5. Importantly, phosphorylation of these proteins by Cdk5 leads to dendritic spine loss, revealing a potential mechanism by which Cdk5 regulates synapse remodeling. Furthermore, Cdk5-dependent phosphorylation of ephexin1 is required for the ephrin-A1 mediated spine retraction, pointing to a critical role of Cdk5 in conveying signals from extracellular cues to actin cytoskeleton at synapses. Taken together, understanding the precise regulation of Cdk5 and its downstream targets at synapses would provide important insights into the multi-regulatory roles of Cdk5 in actin remodeling during dendritic spine development.
新出现的证据表明,细胞周期蛋白依赖性激酶5(Cdk5)在突触可塑性以及学习和记忆等高级脑功能中具有调节作用。然而,Cdk5在突触处作用的分子和细胞机制仍不清楚。最近的研究结果表明,Cdk5通过调节肌动蛋白动力学来调节树突棘形态发生。Ephexin1和WAVE-1是肌动蛋白细胞骨架的两个重要调节因子,最近都被确定为Cdk5的底物。重要的是,Cdk5对这些蛋白质的磷酸化导致树突棘丢失,揭示了Cdk5调节突触重塑的潜在机制。此外,ephrin-A1介导的树突棘回缩需要Cdk5依赖的Ephexin1磷酸化,这表明Cdk5在将细胞外信号传递到突触处的肌动蛋白细胞骨架中起着关键作用。综上所述,了解Cdk5及其在突触处的下游靶点的精确调节,将为Cdk5在树突棘发育过程中肌动蛋白重塑的多重调节作用提供重要见解。